ProSci Catalog

Antibody Product list

13100 Kirkham Way Tel: 858-513-2638
Suite 207 1-888-513-9525
Poway, CA 92064 Fax: 858-513-2692
www.prosci-inc.com
orders@prosci-inc.com
Antibody Listed by Category
Product Name Cat. No. Species Application Description Release Date
Apoptosis-Chromatin condensation and DNA fragmentation factors
Acinus (CP) 2215 H WB Inducer of chromatin condensation 4thQ 2000
Acinus (CT) 2217 H WB Inducer of chromatin condensation 4thQ 2000
Acinus (IN) 2219 H WB Inducer of chromatin condensation 4thQ 2000
Acinus (NP) 2241 H WB Inducer of chromatin condensation 4thQ 2000
AIF (CT) 2301 H M R WB Apoptosis Inducing Factor 4thQ 2000
AIF (IN) 2267 H M R WB Apoptosis Inducing Factor
AIF (NT) 2239 H WB Apoptosis Inducing Factor
CAD / DFF40 (CT) 2011 M WB Caspase Activated DNase
CAD / DFF40 (I17) 2007 M R WB Caspase Activated DNase
CIDE-A (CT) 2085 H WB Cell death-Inducing DFF-like Effector
CIDE-A (CT) 2089 M WB Cell death-Inducing DFF-like Effector 3rdQ 2000
CIDE-B (CT) 2091 M WB Cell death-Inducing DFF-like Effector
DFF40 / CAD (I18) 2107 H M R WB Caspase Activated DNase
DFF40 / CAD (IN) 2155 H WB Caspase Activated DNase
DFF40 / CAD (NT) 2153 H WB Caspase Activated DNase
DFF45 / ICAD (CT) 1141 H WB DNA fragmentation factor & Inhibitor of CAD
DFF45 / ICAD (NT) 1148 H WB, IHC DNA fragmentation factor & Inhibitor of CAD
DNase II (CT) 2059 H WB DNase involved in apoptosis
EndoG 3035 H M R WB Endonuclease G New
ICAD / DFF45 (CT) 2003 M WB, IHC Inhibitor of CAD
ICAD / DFF45 (NT) 2001 M WB, IHC Inhibitor of CAD
Apoptosis-Caspases
Casp-9 / Mch6 / Apaf-3 (IN1) 2071 H WB A new caspase
Casp-9 / Mch6 / Apaf-3 (IN2) 2073 H WB A new caspase
Casp-10 / FLICE2 (CT) 1128 H M R WB A new caspase
Casp-12 (IN) 2327 H M R WB, IHC A new caspase 4thQ 2000
Casp-12 (NT) 2325 H M R WB A casp. in Apoptosis & Alzheimer's Disease 4thQ 2000
Casp-13 / ERICE 2245 H M R WB Evolutionarily Related ICE
Apoptosis-CED4 homologue
Apaf-1 (CT) 2015 H M R WB Apoptosis Protease Activating Factor
Apaf-1 (NT) 2013 H M R WB Apoptosis Protease Activating Factor
FLASH (CT) 2271 H WB Homolog of CED4 4thQ 2000
Apoptosis-BcI-2 family
Bcl10 / CIPER/ CLAP (NT) 2161 H WB, IHC Involved in apoptosis and tumor 4thQ 2000
Bim / BOD (IN) 2065 H M R WB A new member in Bcl-2 family
Bmf (CT) 3029 H WB A new member in Bcl-2 family New
Bmf (NT) 3031 H M WB A new member in Bcl-2 family New
Bnip3L / Nix (IN) 2289 H WB A new member in Bcl2 family 4thQ 2000
PUMA (CT) bbc3 3041 H M WB A novel member in Bcl-2 family New
PUMA (NT) bbc3 3043 H WB A novel member in Bcl-2 family New

Product Name Cat. No. Species Application Description Release Date
Apoptosis-TRAIL and TRAIL receptors
DcR1 / TRAIL-R3 (ED) 2179 H M R WB Decoy Receptor 1 for TRAIL
DcR1 / TRAIL-R3 (ED2) 2299 H M R WB Decoy Receptor 1 for TRAIL 3rdQ 2000
DcR2 / TRAIL-R4 (ID) 2021 H M R WB Decoy Receptor 2 for TRAIL
DR4 / TRAIL-R1 (CT) 1139 H WB Death Receptor for TRAIL
DR4 / TRAIL-R1 (NT) 1167 H WB Death Receptor for TRAIL
DR5 / TRAIL-R2 2019 H M WB Death Receptor for TRAIL
TRAIL / Apo-2L (CT) 1113 H WB Ligand for DR4 and DR5
Apoptosis-Other cell death receptors
DR3 / Wsl-1 / Apo-3 (CT) 1120 H M R WB Cell Death Receptor
DR3 / Wsl-1 / Apo-3 (ED) 1158 H M WB Cell Death Receptor
DR3 / Wsl-1 / Apo-3 (NT) 1166 H M WB Cell Death Receptor
DR6 (NT) 2157 H WB Death Receptor 6
Apoptosis-TNF and Fas related molecules
ADAM10 / KUZ (CT) 2051 H WB TNFα converting enzyme
ARTS 3025 H WB An apoptosis related protein New
DcR3 / TR6 (NT) 2140 H M R WB Decoy Receptor for FASL and LIGHT
SODD (NT) 2143 H M R WB Silencer Of Death Domains
TACE/adam17 (CT) 1131 H M R WB TNFα converting enzyme
Apoptosis-Regulating kinases
ASK1 / MAPKKK5 (CT) 1151 H WB Apoptosis Signal-regulation Kinase
DAPK2 2323 H M R WB Death-Associated Protein kinase 2 1stQ 2001
DRAK1 (NT) 2147 H WB DAPK Related Apoptosis-inducing Kinase
DRAK2 (CT) 2149 H WB DAPK Related Apoptosis-inducing Kinase
RICK / RIP2 (CT) 2183 H WB RIP-like Interacting CLARP Kinase
RICK / RIP2 (NT) 2075 H M R WB RIP-like Interacting CLARP Kinase
RIP3 2283 M R WB Mouse Receptor Interacting Protein 3 1stQ 2001
ZIPK (IN) 2067 H M R WB Apoptosis inducing kinase
Apoptosis-Inhibitory molecules
ARC (CT) 2081 H WB Apoptosis Repressor with CARD domain
ARC (NT) 2185 H M R WB Apoptosis Repressor with CARD domain
mFLIP / I-FLICE (CT) 1156 M WB FLICE inhibitory protein
FLIP / I-FLICE (CT) 1161 H M R WB FLICE inhibitory protein
FLIP / I-FLICE (NT) 1159 H M R WB FLICE inhibitory protein
FLIPs (CT) 2055 H WB FLICE inhibitory protein 3rdQ 2000
ILP-2 3017 H M R WB A novel member in IAP family New
Livin, KIAP 2505 H WB A novel member in IAP family New
Smac / DIABLO (CT) 2409 H M R WB IAPs binding protein 1stQ 2001
mSmac / DIABLO (CT) 2411 H M R WB, IHC IAPs binding protein 1stQ 2001
Survivin / TIAP (CT) 2235 H WB, IHC A new inhibitor of apoptosis 3rdQ 2000
Survivin / TIAP (NT) 2233 H WB, IHC A new inhibitor of apoptosis 3rdQ 2000
mSurvivin / TIAP (CT) 2237 M WB, IHC A new inhibitor of apoptosis 4thQ 2000

Product Name Cat. No. Species Application Description Release Date
Apoptosis-Adapter molecules
ASC 2287 H WB A novel CARD-containing adaptor protein 1stQ 2001
CARD9 2515 H WB A new CARD-containing protein New
DEDAF 2227 H M R WB A novel regulator of apoptosis 3rdQ 2001
Daxx (CT) 1163 H M WB Adapter Molecule
F1Aα (CT) 2279 H M R WB A novel death receptor-binding protein 1stQ 2001
RAIDD / CRADD (CT) 1117 H WB Adapter Molecule
RAIDD / CRADD (IN) 1115 H WB Adapter Molecule
Signal Transduction
CIKS/Act1 (CT) 2499 H WB A novel NF-κB activator 3rdQ 2001
CIKS/Act1 (NT) 2501 H WB A novel NF-κB activator 3rdQ 2001
DOK (CT) 1107 H WB Tyrosine kinase substrate p62DOK
IKKα / IKK-1 (C1) 2025 H WB, IHC IκB kinase alpha
IKKα / IKK-1 (C2) 2115 H WB IκB kinase alpha
IKKα / IKK-1 (C3) 2117 H WB IκB kinase alpha
IKKβ / IKK-2 (C3) 2121 H WB IκB kinase beta
IKKε / IKKi (CT) 2329 H WB IκB Kinase epsilon 1stQ 2001
IKKγ / NEMO / FIP3 (NT) 2335 H M R WB IκB Kinase gamma 1stQ 2001
IL-1RAcP (C1) 2131 H WB IL-1R accessory protein
IL-1RAcP (C2) 2129 H WB IL-1R accessory protein
IRAK (CT) 1007 H M R WB, IP IL-1R associated kinase
IRAK-2 (C2) 2123 H WB IL-1R associated kinase
IRAK-2 (CT) 2213 H WB IL-1R Associated Kinase
IRAK-M 2355 H M R WB A novel IL-1R Associated Kinase 1stQ 2001
MADD / DENN (CT) 1150 H M R WB Activator of MAPK pathway
MYD88 (CT) 2127 H M R WB Adapter in IL-1 & LPS signal
MYD88 (IN) 2125 H WB Adapter in IL-1 & LPS signal
NAK/TBK1 (CT) 2351 H M WB NF-κB activating kinase 2ndQ 2001
NIK (CT) 1129 H WB NF-κB inducing kinase
SIRPα / SHPS-1 (CT) 1125 H M R WB Tyrosine kinase substrate
STAT1 (CT) 1021 H M R WB, IP JAK activated transcription
HIV and chemokine receptors
Bonzo / STRL33 (CT) 1170 H WB HIV coreceptor
Bonzo / STRL33 (NT2) 2209 H WB HIV coreceptor
CCR5 (NT) 1112 H WB HIV & chemokine receptor
CCR8 (EL) 2097 H WB HIV & chemokine receptor
CX3CR1 / V28 (EL) 2201 H WB HIV & chemokine receptor
CX3CR1 / V28 (NT) 2093 H M R WB, FACS HIV & chemokine receptor
CXCR4 (EL) 1012 H M WB HIV & chemokine receptor
CXCR4 (NT) 1009 H M WB, IP, IHC HIV & chemokine receptor
DC-SIGN (CT) 2347 H WB A novel HIV biding protein 3rdQ 2001
DC-SIGN (ED) 2349 H WB A novel HIV biding protein 3rdQ 2001
Eotaxin (CT) 1123 H WB CCR3 ligand
GPR15 / BOB (NT) 2101 H M R WB HIV coreceptor

Product Name Cat. No. Species Application Description Release Date
Neurobiology
APP (AβNT) 2133 H M R WB Amyloid protein precursor
APP (CT) 2136 H M R WB Amyloid protein precursor
BACE / Asp2 (CT) 2253 H M WB Beta-site APP Cleaving Enzyme
BACE2 / Asp1 (NT) 2247 H M R WB Beta-site APP Cleaving Enzyme 2 4thQ 2000
BACE2 / Asp1 (CT) 2249 H WB Beta-site APP Cleaving Enzyme 2 4thQ 2000
GFRα-1 / GDNFR α (IN) 1133 H M R WB GDNF receptor
GFRα-2 / GDNFR β (IN) 1135 H M R WB Neurturin receptor
GFRα-3 / GDNFR γ (IN) 1137 H M R WB Persephin receptor
Neurturin 1121 H WB Ligand for GFRα-2
P53 Network
Chk2 (NT) 2391 H M R WB A novel check point kinase 2ndQ 2001
MTBP (IN2) 2447 H WB MDM2 binding protein 2ndQ 2001
p53DINP1, SIP 3045 H M R WB Apoptosis-associated p53 target New
p53R2 (NT) 2383 H M R WB A novel ribonucleotide reductase 2ndQ 2001
PERP 2451 H WB A mediator of p53 induced apoptosis 2ndQ 2001
PID/MTA2 2443 H M R WB Involved in P53 deacetylation 2ndQ 2001
Immunology
APRIL (ED) 2223 H WB A new member in the TNF family 2ndQ 2001
APRIL (ED2) 2415 H M WB A new member in the TNF family 2ndQ 2001
BAFF / BLyS / Thank / Tall-1 (CT) 2221 H M R WB B cell Activating Factor in TNF Family
IL-21 (IN) 2465 H WB Interleukin 21, related to IL2 and IL15 3rdQ 2001
IL21R (ED) 2469 H M R WB Interleukin 21 receptor 3rdQ 2001
IL21R (NT) 2471 H M R WB Interleukin 21 receptor 3rdQ 2001
IL22R (NT) 2497 H R WB Interleukin 22 receptor 3rdQ 2001
IL22R (CT) 2489 H R WB Interleukin 22 receptor 3rdQ 2001
TCCR (NT) 2481 H WB A new T cell cytokine receptor 3rdQ 2001
TCCR (CT) 2483 H WB A new T cell cytokine receptor 3rdQ 2001
WB-Western blot / IHC-immunohistochemistry / IP-immunoprecipitation / NT-N-terminus
CT-C-terminus / ED-extracellular domain / ID-intracellular domain / IN-intermediate domain
NP-N-terminus of the peptide / CP-C-terminus of the peptide
EL-extracelluar loop / FACS-Flow Cytometry / H-human / M-mouse / R-rat

peptide Product list

13100 Kirkham Way Toll free: 888-513-9525
Suite 207 Tel: 858-513-2638
Poway, CA 92064 Fax: 858-513-2692
www.prosci-inc.com
orders@prosci-inc.com
Peptide List
Product Name Cat. No. Source Sequences
Acinus (CP) peptide 2215P Human TRTALHGVKWPQSNPK
Acinus (CT) peptide 2217P Human SRSTPVRDRGGRR
Acinus (IN) peptide 2219P Human DTSENRPENDVPEPP
Acinus (NP) peptide 2241P Human DDPVRTAQVPSPPRGK
ADAM10 (CT) peptide 2051P Human PQRQRPRESYQMGHMRR
AIF (CT) peptide 2301P Human KDGEQHEDLNEVAK
AIF (IN) peptide 2267P Human PKSATEQSGTGIRSE
AIF (NT) peptide 2239P Human KQKKAALSASEGEE
Apaf-1 (CT) peptide 2015P Human TFYTNGTNLKKIHVSPDFKT
Apaf-1 (NT) peptide 2013P Human HREALEKDIKTSYIMDHC
APP (AbNT) peptide 2133P Human CDAEFRHDSGY
APP (CT) peptide 2136P Human CGYENPTYKFFEQMQN
APRIL (ED) peptide 2223P Human GTGGPSQNGEGYP
APRIL (ED2) peptide 2415P Human CIRSMPSHPDRAYNS
ARC (CT) peptide 2081P Human PDPEPEPDFEERDESEDS
ARC (NT) peptide 2185P Human GNAQERPSETIDRERKR
ASC peptide 2287P Human RESQSYLVEDLERS
BACE (CT) peptide 2253P Human CLRQQHDDFADDISLLK
BACE2 (CT) peptide 2249P Human CQRRPRDPEVVNDESS
BACE2 (NT) peptide 2247P Human APTPGPGTPAERHADG
BAFF (CT) peptide 2221P Human EEGDELQLAIPRENAQ
BCL-10 (NT) peptide 2161P Human APSLTEEDLTEVKKDC
Bim (IN) peptide 2065P Human AERPPQLRPGAPTSLQTEP
Bnip3L (IN) peptide 2289P Human DAQHESGQSSSRGSSH
Bonzo (CT) peptide 1170P Human KSSEDNSKTFSASHNVEATS
Bonzo (NT2) peptide 2209P Human GFSSFNDSSQEEHQD
CAD (CT) peptide 2011P Mouse KLECDRSRIYRPQTGS
CAD (I17) peptide 2007P Mouse YNGSYFDRGAEASSRL
Casp-10 (CT) peptide 1128P Human ISAQTPRPPMRRWSSVS
Casp-12 (NT) peptide 2325P Murine AARRTHERDPIYKIKG
Casp-13 peptide 2245P Human ETVAGPDESVGSAAT
Casp-9 (IN1) peptide 2071P Human EDIQRAGSGSRRDQAR
Casp-9 (IN2) peptide 2073P Human ASTSPEDESPGSNPEPDATP
Caspase-12 (IN) peptide 2327P Murine CTPSSPSESKRKVEDDE
CCR5 (NT) peptide 1112P Human SSPIYDINYYTSEPC
CCR8 (EL) peptide 2097P Human CYSFYNQQTLKWKIFTNFK
Chk2 (NT) peptide 2391P Human SRESDVEAQQSHGSSAC
CIDE-A (CT) peptide 2085P Human DDKEERPSLRSQAKGRFT
CIKS/Act1 (CT) peptide 2499P Human REEEYVAPPRGPLPT
CIKS/Act1 (NT) peptide 2501P Human PPQLQETRMNRSIP
CX3CR1 (EL) peptide 2201P Human CLGDYPEVLQEIWPV
CX3CR1 (NT) peptide 2093P Human DQFPESVTENFEYDDLAEAC
CXCR4 (EL) peptide 1012P Human DRYICDRFYPNDLWV
CXCR4 (NT) peptide 1009P Human MEGISIYTSDNYTE
DAP kinase 2 peptide 2323P Human ARRKALHPRRRSSTS
Daxx (CT) peptide 1163P Human TSVATQCDPEEIIVLSDSD
DC-SIGN (CT) peptide 2347P Human CSRDEEQFLSPAPATPNPPPA
DC-SIGN (ED) peptide 2349P Human CYFMSNSQRNWHDSITA
DcR1 (ED) peptide 2179P Human CVEEFGANATVETPAAEET
DcR1 (ED2) peptide 2299P Human CKEGTFRNENSPE

Product Name Cat. No. Source Sequences
DcR2 (ID) peptide 2021P Human GGPERVHRVLFRRRS
DcR3 (NT) peptide 2140P Human AETPTYPWRDAETGERC
DEDAF peptide 2227P Human TPKGDMSAVNDESF
DFF40 (IN) peptide 2155P Human NGSYFDRGAKGGSRLC
DFF40 (NT) peptide 2153P Human QKPKSVKLRALRSPRKC
DFF40/CAD (I18) peptide 2107P Mouse EGLESRFRNKSGYLRYS
DFF45 (CT) peptide 1141P Human KASPPGDLQNPKRARQDPT
DFF45/35 (NT) peptide 1148P Human EVTGDAGVPESGEIRTLKPC
DNase II (CT) peptide 2059P Human CNGMARKPSRAYKI
DR3 (CT) peptide 1120P Human ERMGLDGCVEDLRSRLQRGP
DR3 (ED) peptide 1158P Human APCTEPCGNSTCLVCPQDT
DR3 (NT) peptide 1166P Human QGGTRSPRCDCAGDFH
DR4 (CT) peptide 1139P Human CDSGKFIYLEDGTGSAVSLE
DR4 (NT) peptide 1167P Human ASGTEAAAATPSKVWGSSAG
DR5 (CT) peptide 2019P Human KIEDHLLSSGKFMYLEGNAD
DR6 (NT) peptide 2157P Human QPEQKASNLIGTYRHC
DRAK1 (NT) peptide 2147P Human EKPGSGGSSPGATSGC
DRAK2 (CT) peptide 2149P Human CSKRFRFDDSLPNPHE
Eotaxin peptide 1123P Human DSMKYLDQKSPTPKP
F1Aα peptide 2279P Human DINYQDQIPRTLEE
FLASH (CT) peptide 2271P Human SERFQQLMKLFEKSKC
FLIP (CT) peptide 1161P Human NGYMYDWNSRVSAKEKYY
FLIP (NT) peptide 1159P Human SAEVIHQVEEALDTDEKE
FLIPs (CT) peptide 2055P Human QKSLKDPSNNFRMITPYAH
GFRα-1 (IN) peptide 1133P Human KNKPLGPAGSENEI
GFRα-3 (IN) peptide 1137P Human RFHRQLFSQDWADS
GPR15 (NT) peptide 2101P Human YYATSPNSDIRETHSH
ICAD (CT) peptide 2003P Mouse RRSPLPGEPQRPKRAKRDSS
ICAD (NT) peptide 2001P Mouse ELSRGASAPDPDDVRPLKPC
IKKα (C1) peptide 2025P Human CLGHLSTIIHEANEEQGNS
IKKα (C2) peptide 2115P Human TPQDGETSAQMIEENLN
IKKα (C3) peptide 2117P Human CTQSSARSLVGSSLEGA
IKKβ (C3) peptide 2121P Human CSKVRGPVSGSPDSMNASR
IKKε/IKK-i (CT) peptide 2329P Human NRIIERLNRVPAPPDV
IKKγ/NEMO (NT) 2335P Human CQYQAPDMDTLQIHVME
IL-1RAcP (C2) peptide 2129P Human KWKGEKSKYPQGRFWK
IL-1RAcP (CT) peptide 2131P Human KKSPRRSSSDEQGLSYSSLKN
IL-21 (IN) peptide 2465P Human TCPSCDSYEKKPPKE
IL-21R (ED) peptide 2469P Human NITDQSGNYSQECGS
IL-21R (NT) peptide 2471P Human CPDLVCYTDYLQT
IL-22R (CT) peptide 2489P Human DSLFRGLALTVQWES
IL-22R (NT) peptide 2497P Human QSSNFENILTWDSGPE
IRAK (CT) peptide 1007P Human DRQGPEESDEFQS
IRAK-M peptide 2355P Human CSSKFSWDEYEQYKKE
IRAK2 (C2) peptide 2123P Human APWAGAATPLLPTENGEGR
IRAK2 (CT) peptide 2213P Human READSSSEACVGLEPPQDVT
MADD (CT) peptide 1150P Human AAVHSSEEDLRTPPRPVSS
mCIDE-A (CT) peptide 2089P Mouse GDTEEQPSPKPSTKG
mCIDE-B (CT) peptide 2091P Mouse EGADRWQWHGQRHLHS
mFLIP (CT) peptide 1156P Mouse DKVYAWNSGVSSKEKYS
mSmac/DIABLO (CT) peptide 2411P Murine SDEGADQEEEAYLRED
MyD88 (CT) peptide 2127P Human CTKSWFWTRLAKALSLP
MyD88 (IN) peptide 2125P Human CDFQTKFALSLSPGAHD
MTBP (IN2) peptide 2447P Human GAVECFEEEDSNSRESLS
NAK/TBK1 (CT) peptide 2351P Human ERFGSLTMDGGLRNVD

Product Name Cat. No. Source Sequences
NIK (CT) peptide 1129P Human SFAWSWRVKHGQLENRP
NTN (NT) peptide 1121P Human DAHSRYHTVHELSARE
p53R2 (NT) peptide 2383P Human GDPERPEAAGLDQDER
PID/MTA2 peptide 2443P Human PAPSHPASTNEPIVLED
RAIDD (CT) peptide 1117P Human CHNGLRAVEVDPSLLLHMLE
RAIDD (IN) peptide 1115P Human CAGDRLTGIPSHILNSSPSD
RICK (CT) peptide 2183P Human KLKDNKQMGLQPYPE
RICK (NT) peptide 2075P Human PTIPYHKLADLRYLSRGASG
RIP3 peptide 2283P Murine AQFGRGRGWQPFHK
SIRPα (CT) peptide 1125P Human KPEPSFSEYASVQVPRK
Smac/DIABLO (CT) peptide 2409P Human EERAESEQEAYLRED
SODD (NT) peptide 2143P Human SALRRSGYGPSDGPSC
Survivin (CT) peptide 2235P Human CKKVRRAIEQLAAMD
Survivin (NT) peptide 2233P Human MGAPTLPPAWQP
Survivin peptide 2237P Mouse AKTTRQSIEQLAA
TACE (CT) peptide 1131P Human ASFKLQRQNRVDSKETE
TRAIL (CT) peptide 1113P Human CTNEHLIDMDHEASFFGA
ZIPK (IN) peptide 2067P Human RRRNVRGEDSGRKPERRRLK

lysate Product list

13100 Kirkham Way Toll free: 888-513-9525
Suite 207 Tel: 858-513-2638
Poway, CA 92064 Fax: 858-513-2692
www.prosci-inc.com
orders@prosci-inc.com
Product Name Catalog No. Application Size
Cell Lysate
293 whole cell lysate 1210 Western blot 200 µg
3T3 whole cell lysate 1212 Western blot 200 µg
U937 whole cell lysate 1215 Western blot 200 µg
A431 whole cell lysate 1202 Western blot 200 µg
A549 whole cell lysate 1203 Western blot 200 µg
HeLa whole cell lysate 1201 Western blot 200 µg
HepG2 whole cell lysate 1211 Western blot 200 µg
HL60 whole cell lysate 1209 Western blot 200 µg
Jurkat whole cell lysate 1205 Western blot 200 µg
K562 whole cell lysate 1204 Western blot 200 µg
MDA-MB-361 whole cell lysate 1217 Western blot 200 µg
MOLT4 whole cell lysate 1206 Western blot 200 µg
PC-3 whole cell lysate 1216 Western blot 200 µg
Raji whole cell lysate 1207 Western blot 200 µg
SW1353 whole cell lysate 1214 Western blot 200 µg
T24 whole cell lysate 1213 Western blot 200 µg
THP-1 whole cell lysate 1208 Western blot 200 µg
Human Tissue Lysate
Human brain tissue lysate 1303 Western blot 200 µg
Human heart tissue lysate 1301 Western blot 200 µg
Human kidney tissue lysate 1305 Western blot 200 µg
Human liver tissue lysate 1304 Western blot 200 µg
Human lung tissue lysate 1302 Western blot 200 µg
Human pancreas tissue lysate 1307 Western blot 200 µg
Human small intestine tissue lysate 1308 Western blot 200 µg
Human spleen tissue lysate 1306 Western blot 200 µg
Human Tumor Tissue Lysate
Lysate List
Human brain tumor lysate 1322 Western blot 200 µg
Human breast tumor lysate 1323 Western blot 200 µg
Human colon normal tissue lysate 1341-N Western blot 200 µg
Human colon tumor tissue lysate 1341-T Western blot 200 µg
Human kidney tumor lysate 1324 Western blot 200 µg
Human liver normal tissue lysate 1342-N Western blot 200 µg
Human liver tumor tissue lysate 1342-T Western blot 200 µg
Human lung tumor lysate 1321 Western blot 200 µg

Product Name Catalog No. Application Size
Mouse Tissue Lysate
Mouse brain tissue lysate 1403 Western blot 200 µg
Mouse heart tissue lysate 1401 Western blot 200 µg
Mouse kidney tissue lysate 1405 Western blot 200 µg
Mouse liver tissue lysate 1404 Western blot 200 µg
Mouse lung tissue lysate 1402 Western blot 200 µg
Mouse skeletal muscle tissue lysate 1407 Western blot 200 µg
Mouse small intestine tissue lysate 1408 Western blot 200 µg
Mouse spleen tissue lysate 1406 Western blot 200 µg
Rat Tissue Lysate
Rat brain tissue lysate 1463 Western blot 200 µg
Rat kidney tissue lysate 1465 Western blot 200 µg
Rat liver tissue lysate 1464 Western blot 200 µg
Rat lung tissue lysate 1462 Western blot 200 µg
Rat skeletal muscle tissue lysate 1467 Western blot 200 µg
Rat spleen tissue lysate 1466 Western blot 200 µg

Antibody Data Sheets

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IRAK (CT)
CATALOG No.: 1007
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα and
LPS. A serine/threonine protein kinase associated with IL-1
receptor (IRAK) and its homologue mouse pelle-like protein
kinase (mPLK) were identified recently (1,2). IRAK is
associated with the IL-1 receptor subunits IL-1RI and IL-
1RAcP after IL-1 binding and serves as a signaling molecule
to mediate IL-1 response (3). IRAK mediates a signaling
cascade leading to NF-κB activation by members in IL-1
family including IL-1 and a novel cytokine IL-18 (also termed
IGIF) (1,4).
SOURCE:
Rabbit anti-IRAK polyclonal antibody was raised against a
peptide corresponding to amino acids 700 to 712 of human
IRAK (1).
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:1000 dilution and for immunoprecipitation with 2 to 4 µg
per sample. THP-1 or HeLa whole cell lysate can be used as
positive control and an 80 kDa band should be detected in
the lysate from non-activated cells. It is human, mouse, and
rat reactive, and has no cross response to IRAK2. For
research use only.
STORAGE: It is supplied as purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis of IRAK
in THP-1 (THP) and HeLa
(HL) whole cell lysates with
anti-IRAK at 1:2000 dilution.
REFERENCES:
1. Cao Z; Henzel WJ; Gao X. IRAK: a kinase associated with the
interleukin-1 receptor. Science 1996;271:1128-31.
2. Trofimova M; Sprenkle AB; Green M; Sturgill TW; Goebl MG;
Harrington MA. Developmental and tissue-specific expression of
mouse pelle-like protein kinase. J Bio Chem 1996; 271: 17609-
12.
3. Jianing Huang, Xiong Gao, Shyun Li, and Zhaodan Cao.
Recruitment of IRAK to the interleukin 1 receptor complex requires
interleukin-1 receptor accessory protein. Proc Natl Acad Sci USA
1997;94:12829-12832
4. Robinson D, Shibuya K, Mui A, Zonin F, Murphy E, Sana T,
Hartley SB, Menon S, Kastelein R, Bazan F, O'Garra A. IGIF does
not drive Th1 development but synergizes with IL-12 for interferongamma
production and activates IRAK and NF-κB. Immunity
1997;7:571-581
(RD1299)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-CXCR4 (NT) Fusin, LESTR, HUMSTR
CATALOG NO.: 1009
BACKGROUND:
Human immunodeficiency virus (HIV) and related viruses
require coreceptors, in addition to CD4, to infect target cells.
Some G protein-coupled receptors including CCR5, CXCR4,
CCR3, CCR2b and CCR8 in the chemokine receptor family,
and four new human molecules GPR15, STRL33, GPR1 and
V28 were recently identified as HIV coreceptors (1). Among
them, CXCR4 (fusin, LESTR or HUMSTR) is a principal
coreceptor for T-cell tropic strains of HIV-1 fusion and entry
of human white blood cells (2,3). CXCR4 is also required for
the infection by dual-tropic strains of HIV-1 and mediates
CD-4 independent infection by HIV-2 (4,5). The α-chemokine
SDF-1 is the ligand for CXCR4 and prevents infection by T-
tropic HIV-1 (6,7). CXCR4 associates with the surface CD4-
gp120 complex before HIV enters target cells (8). CXCR4
messenger RNA levels correlated with HIV-1 permissiveness
in diverse human cell types (2). Antibodies to CXCR4 block
HIV-1 and HIV-2 fusion and infection of human target cells
(2,5,10). The amino-terminal domain and the second
extracellular loop of CXCR4 serve as HIV binding sites
(10,11).
SOURCE:
Rabbit anti-CXCR-4 polyclonal antibody was raised against a
peptide corresponding to amino acids 1 to 14 of human
CXCR4 (3,9).
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:1000 to 1:2000 dilution and for immunoprecipitation and
immunocytochemistry. HeLa whole cell lysate can be used
as positive control. It is human and mouse reactive. For
research use only.
Western blot analysis of
CXCR4 in HeLa total cell
lysate with anti-CXCR4 (NT)
at 1:2000 dilution.
REFERENCES:
1. Dimitrov DS. Cell 1997;91:721-730
2. Feng Y et al. Science 1996;272:872-7.
3. Berson JF et al. J Virol 1996;70:6288-95.
4. Doranz BJ et al. Cell 1996;85:1149-1158
5. Endres MJ et al. Cell 1996;87:745-756
6. Bleul CC et al. Nature 1996;382:829-833
7. Oberlin E et al. Nature 1996;382:833-835
8. Lapham CK et al. Science 1996;274:602-5.
9. Leoetscher M et al. J Biol Chem 1994;269:232-237
10. Brelot A et al. J Virol 1997;71:4744--954751.
11. Lu Z et al. Proc Natl Acad Sci USA 1997;94:6426-6431
(RD1299)
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable for
one year.

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Anti-CXCR4 (EL) Fusin, LESTR, HUMSTR
CATALOG NO.: 1012
BACKGROUND:
Human immunodeficiency virus (HIV) and related viruses
require coreceptors, in addition to CD4, to infect target cells.
Some G protein-coupled receptors including CCR5, CXCR4,
CCR3, CCR2b and CCR8 in the chemokine receptor family,
and four new human molecules GPR15, STRL33, GPR1 and
V28 were recently identified as HIV coreceptors (1). Among
them, CXCR4 (fusin, LESTR or HUMSTR) is a principal
coreceptor for T-cell tropic strains of HIV-1 fusion and entry
of human white blood cells (2,3). CXCR4 is also required for
the infection by dual-tropic strains of HIV-1 and mediates
CD-4 independent infection by HIV-2 (4,5). The α-chemokine
SDF-1 is the ligand for CXCR4 and prevents infection by T-
tropic HIV-1 (6,7). CXCR4 associates with the surface CD4-
gp120 complex before HIV enters target cells (8). CXCR4
messenger RNA levels correlated with HIV-1 permissiveness
in diverse human cell types (2). Antibodies to CXCR4 block
HIV-1 and HIV-2 fusion and infection of human target cells
(2,5,10). The amino-terminal domain and the second
extracellular loop of CXCR4 serve as HIV biding sites
(10,11).
APPLICATION: This polyclonal antibody can be used for
Western blot at 1:500 to 1:1000 dilution. HeLa whole cell
lysate can be used as positive control. It is human and
mouse reactive. For research use only.
SOURCE:
Rabbit anti-CXCR-4 polyclonal antibody was raised
against a peptide corresponding to amino acids 182 to 196
in the second extracellular loop (EL) of human CXCR4
(3,9).
Western blot analysis of
CXCR4 in HeLa total cell
lysate with anti-CXCR4
(EL) at 1:1000 dilution.
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
REFERENCES:
1. Dimitrov DS. Cell 1997;91:721-730
2. Feng Y et al. Science 1996;272:872-7.
3. Berson JF et al. J Virol 1996;70:6288-95.
4. Doranz BJ et al. Cell 1996;85:1149-1158
5. Endres MJ et al. Cell 1996;87:745-756
6. Bleul CC et al. Nature 1996;382:829-833
7. Oberlin E et al. Nature 1996;382:833-835
8. Lapham CK et al. Science 1996;274:602-5.
9. Leoetscher M et al. J Biol Chem 1994;269:232-237
10. Brelot A et al. J Virol 1997;71:4744--954751
11. Lu Z et al. Proc Natl Acad Sci USA 1997;94:6426-6431
(RD1299)

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techsupport@prosci-inc.com
Anti-STAT1α
CATALOG No.: 1021
BACKGROUND:
STATs (signal transducers and activators of transcription)
are a family of cytoplasmic latent transcription factors that
are activated to regulate gene expression in response to a
large number of extracellular signaling polypeptides
including cytokines, interferons, and growth factors. After
phosphorylation by JAK tyrosine kinases, STATs enter the
nucleus to regulate transcription of many different genes.
Among the seven STATs (Stat1, Stat2, Stat3, Stat4, Stat5a,
Stat5b, and Stat6), Stat1, Stat3, Stat5a, and Stat5b have a
wide activation profile (1,2). STAT1 is activated by many
different ligands including IFN family (IFN-α, IFN-β, IFN-γ
and IL-10), gp130 family (IL-6, IL-11, LIF, CNTF, and G-
CSF), and receptor tyrosine kinases (EGF, PDGF, and CSF-
1) (3). STAT1 has two forms, the 91 kDa STAT1α and the
84 kDa STAT1β which are encoded by the same gene with
splicing variant (4).
SOURCE:
Rabbit anti-STAT1α polyclonal antibody was raised against
a peptide corresponding to amino acids 712 to 750 of human
STAT1α (4). The sequences differ from the murine
corresponding sequences by four amino acids.
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:1000 to 1:2000 and for immunoprecipitation at 2 to 4 µg
per sample. It is human, mouse, and rat reactive. Whole cell
lysate from HeLa, Jurkat, or A431 cells can be used as
positive control and a 91 kDa band can be detected. No
reaction to the 84 kDa STAT1β. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
Western blot analysis
of STAT1α in whole
cell lysates from HeLa
(H), Jurkat (J), A431
(A), K562 (K), and
NIH3T3 (N) cells,
respectively, with anti-
STAT1α at 1:1000
dilution.
REFERENCES:
1. Leonard WJ, O'Shea JJ. Jaks and STATs: biological
implications. Annu Rev Immunol 1998;16:293-322.
2. Schindler C, Darnell JE Jr. Transcriptional responses to
polypeptide ligands: the JAK-STAT pathway. Annu Rev Biochem
1995;64:621-51.
3. Darnell JE Jr. STATs and gene regulation. Science
1997;277:1630-5.
4. Schindler C, Fu XY, Improta T, Aebersold R, Darnell JE Jr.
Proteins of transcription factor IS GF-3: one gene encodes the 91-
and 84-kDa ISGF-3 proteins that are activated by interferon alpha.
Proc Natl Acad Sci USA 1992;89:7836
(RD1299)

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techsupport@prosci-inc.com
Anti-p62 dok
CATALOG No.: 1107
STORAGE:
It is supplied as affinity purified IgG with immunogenic
BACKGROUND:
Signals from most growth factors and cytokines are
peptide, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at -20°C. Stable for one year at 2-8°C.
transduced by receptor tyrosine kinases or non-receptor
tyrosine kinases. Activated tyrosine kinases phosphorylate
their substrates, which mediate the cellular response to
extracellular stimuli. A long-sought major substrate termed
p62 dok (downstream of tyrosine kinase) for many tyrosine
kinases including c-kit, v-abl, v-Fps, v-Src, v-Fms, and
activated EGF, PDGF, IGF, VEGF and insulin receptors was
Western blot analysis of
p62 dok in Jurkat (Jur) and
THP-1 (THP) total cell
lysates with anti-p62 dok at
1:1000 dilution.
identified recently from human and mouse by several
laboratories (1,2). Upon phosphorylation, p62 dok
forms a
complex with the ras GTPase-activating protein (RasGAP)
(1-3). p62 dok represents a new family with very recently
identified p56 dok (4)
SOURCE:
Rabbit anti-p62 dok polyclonal antibody was raised against a
peptide corresponding to amino acids 425 to 439 of human
p62 dok (1).
APPLICATION:
This polyclonal antibody can be used for detection of p62 dok
expression by Western blot at 1:1000 to 1:2000 dilution.
Whole cell lysate from Jurkat cells can be used as positive
control and a 62 kDa band should be detected. This antibody
is for research use only.
REFERENCES:
1. Carpino N, Wisniewski D, Strife A, Marshak D, Kobayashi R,
Stillman B, Clarkson B p62(dok): a constitutively tyrosinephosphorylated,
GAP-associated protein in chronic myelogenous
leukemia progenitor cells. Cell 1997;88:197-204.
2. Yamanashi Y, Baltimore D Identification of the Abl- and rasGAPassociated
62 KDa protein as a docking protein, Dok. Cell
1997;88:205-211.
3. Holland SJ, Gale NW, Gish GD, Roth RA, Songyang Z, Cantley
LC, Henkemeyer M, Yancopoulos GD, Pawson T. Juxtamembrane
tyrosine residues couple the Eph family receptor EphB2/Nuk to
specific SH2 domain proteins in neuronal cells. EMBO J
1997;16:3877-3888.
4. Di Cristofano A, Carpino N, Dunant N, Friedland G, Kobayashi
R, Strife A, Wisniewski D, Clarkson B, Pandolfi PP, Resh MD.
Molecular cloning and characterization of p56(dok-2) defines a new
family of RasGAP-binding proteins. J Biol Chem 1998;273:4827-
4830.
(RD1299)

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Anti-CCR5 (NT)
CATALOG NO.: 1112
BACKGROUND:
Human immunodeficiency virus (HIV) and related virus
require coreceptors, in addition to CD4, to infect target cells.
Some G protein-coupled receptors including CCR5, CXCR4,
CCR3, CCR2b and CCR8 in the chemokine receptor family,
and four new human molecules GPR15, STRL33, GPR1 and
V28 were recently identified as HIV coreceptors (1,2).
Among them, CCR5 (CC-CKR-5) is a principal coreceptor for
macrophage- and dual-tropic HIV-1 strains fusion and entry
of human white blood cells (3,4). CCR5 is required for the
infection by HIV-1, HIV-2, and SIV (1,2). The β-chemokines
RANTES, MIP-1α and MIP-1β are the ligands for CCR5 and
prevent infection by M-tropic HIV-1 (3-5). CXC5 associates
with the surface CD4-gp120 of HIV complex and leads to
membrane fusion and virus entry of target cells (6,7). The
amino-terminal domain and the extracellular loops of CCR5
serve as HIV biding sites (8,9). CCR5 messenger RNA is
expressed in lymphoid organs and monocytes.
SOURCE:
Rabbit anti-CCR5 polyclonal antibody was raised against a
peptide corresponding to amino acids 6 to 20 of human
CCR5 (10,11).
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:1000 to 1:2000 dilution. THP-1 whole cell lysate can be
used as positive control and an approximate 40 kDa band
can be detected. For research use only.
Western blot analysis of
CCR5 in THP-1 whole cell
lysate with anti-CCR5 (NT)
at 1:1000 dilution.
REFERENCES:
1. Dimitrov, DS. Cell 1997;91:721-30
2. Littman, DR. Cell 1998;93:677-80
3. Deng, H, et al. Nature 1996;381:661-6
4. Dragic, T, et al. Nature 1996;381:667-73
5. Coochi, F. et al. Science 1995;270:1811-5.
6. Wu, L. et al. Nature 1996;384:179-83
7. Trkola , A. et al. Nature 1996;384:184-7
8. Doranz, BJ. et al. J Virol 1997;71:6305-14
9. Dragic, T, et al. J Virol 1998;72:279-85
10. Raport, CJ, et al. J Biol Chem 1996;271:17161-6
11. Combadiere, C. et al. J Leuk Biol 1996;60:147-52
(RD0900)
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.

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Anti-TRAIL (CT) Apo-2L
CATALOG No.: 1113
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand in the TNF family through their
death domain containing receptors, TNFR1 and Fas. A novel
member in the TNF family was recently identified and
designated TRAIL (for TNF-related apoptosis-inducing
ligand) and Apo-2L (for Apo-2 ligand) 1,2 . TRAIL is a type II
membrane protein and expressed in a variety of human
tissues. Two novel death domain containing receptors DR4
and DR5 have been identified as the receptor for TRAIL 3-6 .
Like TNF and Fas ligand, TRAIL induces apoptosis and NFκB
activation in many tissues and cells.
SOURCE:
Rabbit anti-TRAIL (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 261 to 277
of human TRAIL (1).
APPLICATION:
This polyclonal antibody can be used for detection of TRAIL
by Western blot at 1:500 dilution. For research use only.
STORAGE:
It is supplied as ion chromatography purified IgG, 100 µg in
200 µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year. Azide free antibody is available.
Western blot analysis of
TRAIL in HeLa cell lysate
containing 10, 2.5, or 1 ng of
recombinant protein
containing extracellular
domain of TRAIL with anti-
TRAIL (CT) at 1 µg/ml.
REFERENCES:
1. Wiley SR, Schooley K, Smolak PJ, Din WS, Huang CP, Nicholl
JK, Sutherland GR, Smith TD, Rauch C, Smith CA, et al.
Identification and characterization of a new member of the TNF
family that induces apoptosis. Immunity 1995;3:673-682
2. Pitti RM; Marsters SA; Ruppert S; Donahue CJ; Moore A;
Ashkenazi A. Induction of apoptosis by Apo-2 ligand, a new
member of the tumor necrosis factor cytokine family. J. Biol. Chem.
1996;271:12687-90
3. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R;
Ebner R; Ni J; Dixit VM. The receptor for the cytotoxic ligand
TRAIL. Science; 1997;276:111-113
4. Schneider P, Thome M, Burns K, Bodmer JL, Hofmann K,
Kataoka T, Holler N, Tschopp J. TRAIL receptors 1 (DR4) and 2
(DR5) signal FADD-dependent apoptosis and activate NF-κB.
Immunity 1997;7:831-836
5. Pan G, Ni J, Wei YF, Yu G, Gentz R, Dixit VM. An antagonist
decoy receptor and a death domain-containing receptor for TRAIL.
Science 1997;277:815-818
6. Sheridan JP, Marsters SA, Pitti RM, Gurney A, Skubatch M,
Baldwin D, Ramakrishnan L, Gray CL, Baker K, Wood WI,
Goddard AD, Godowski P, Ashkenazi A. Control of TRAIL-induced
apoptosis by a family of signaling and decoy receptors. Science
1997;277:818-821
(RD0500)

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Anti-RAIDD (IN) CRADD
CATALOG No.: 1115
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain (DD)-containing receptors, TNFR1 and Fas.
The death signals are transduced by a group of DDcontaining
adapter molecules. A novel cell death adapter
was recently identified by two independent groups and
designated RAIDD (RIP-associated ICH-1/CED-3-
homologous protein with DD) and CRADD (caspase and RIP
adapter with DD) 1,2 . RAIDD contains a DD and a CARD (for
caspase recruitment domain) which interact with RIP and
caspase, respectively, to transduce death signals 1,3 . RAIDD
is constitutively expressed in many tissues and mediates
apoptosis caused by Fas and TNFR-1.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis of
RAIDD in whole cell
lysates from HeLa (H) or
K562 (K) cells with anti-
RAIDD (IN) at 1:500
dilution.
REFERENCES:
1. Duan H, Dixit VM. RAIDD is a new 'death' adaptor molecule.
Nature 1997;385:86-89
SOURCE:
Rabbit anti-RAIDD (IN) polyclonal antibody was raised
against a peptide corresponding to amino acids 99 to 117 of
human RAIDD 1 .
APPLICATION:
This polyclonal antibody can be used for detection of RAIDD
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from HeLa or K562 cells can be used as positive control and
a 22 kDa band should be detected. This antibody is for
research use only.
2. Ahmad M, Srinivasula SM, Wang L, Talanian RV, Litwack G,
Fernandes-Alnemri T, Alnemri ES. CRADD, a novel human
apoptotic adaptor molecule for caspase-2, and FasL/tumor
necrosis factor receptor-interacting protein RIP. Cancer Res 1997
57:615-619
3. Hofmann K, Bucher P, Tschopp J. The CARD domain: a new
apoptotic signalling motif. Trends Biochem Sci 1997;22:155-15
(RD1299)

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Anti-RAIDD (CT) CRADD
CATALOG No.: 1117
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain (DD)-containing receptors, TNFR1 and Fas.
The death signals are transduced by a group of DDcontaining
adapter molecules. A novel cell death adapter
was recently identified by two independent groups and
designated RAIDD (RIP-associated ICH-1/CED-3-
homologous protein with DD) and CRADD (caspase and RIP
adapter with DD) 1,2 . RAIDD contains a DD and a CARD (for
caspase recruitment domain) which interact with RIP and
caspase, respectively, to transduce death signals 1,3 . RAIDD
is constitutively expressed in many tissues and mediates
apoptosis caused by Fas and TNFR-1.
SOURCE:
Rabbit anti-RAIDD (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 181 to 199
of human RAIDD 1 .
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis of
RAIDD in HeLa total cell lysate
with anti-RAIDD (CT) at 1:500
dilution.
REFERENCES:
1. Duan H, Dixit VM. RAIDD is a new 'death' adaptor
molecule. Nature 1997;385:86-89
2. Ahmad M, Srinivasula SM, Wang L, Talanian RV,
Litwack G, Fernandes-Alnemri T, Alnemri ES. CRADD, a
novel human apoptotic adaptor molecule for caspase-2,
and FasL/tumor necrosis factor receptor-interacting protein
RIP. Cancer Res 1997 57:615-619
APPLICATION:
This polyclonal antibody can be used for detection of RAIDD
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from HeLa cells can be used as positive control and a major
22 kDa band should be detected. This antibody is for
research use only.
3. Hofmann K, Bucher P, Tschopp J. The CARD domain: a
new apoptotic signalling motif. Trends Biochem Sci
1997;22:155-15
(RD1299)

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Anti-DR3 (CT) Wsl-1, Apo-3, TRAMP, LARD
CATALOG No.: 1120
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain containing receptors, TNFR1 and Fas. A novel
cell death receptor was recently identified by several groups
independently and designated DR3, Wsl-1, Apo-3, TRAMP
and LARD 1-5 . The ligand for this novel cell death receptor
has not yet been defined. DR3 is highly expressed in the
tissues enriched in lymphocytes including PBL, thymus and
spleen. Like TNFR1, DR3 induces apoptosis and NF-κB
activation.
SOURCE:
Rabbit anti-DR3 (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 398 to 417 of human
DR3 1,2 .
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:500 to 1:1000 dilution. Jurkat total cell lysate can be used
as positive control and a 59 kDa band should be detected. It
is human, mouse, and rat reactive and has no cross reaction
to other death receptors. For research use only.
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis of
DR3 in Jurkat total cell
lysate with anti-DR3 (CT)
at 1:500 dilution.
REFERENCES:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan
DR; Xing L; Gentz R; Ni J; Dixit VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT;
Grinham CJ; Brown R; Farrow SN. Nature, 1996;384:372-5.
3. Marsters SA; Sheridan JP; Donahue CJ; Pitti RM; Gray CL;
Goddard AD; Bauer KD; Ashkenazi A. Curr Biol, 1996;6:1669-76.
4. Bodmer JL; Burns K; Schneider P; Hofmann K; Steiner V;
Thome M; Bornand T; Hahne M; Schroter M; Becker K; et al.
Immunity, 1997;6:79-88.
5. Screaton GR; Xu XN; Olsen AL; Cowper AE; Tan R; McMichael
AJ; Bell JI. Proc. Nat. Acad. Sci. USA. 1997;94:4615-9.
(RD1299)

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Anti- Neurturin
CATALOG No.: 1121
BACKGROUND:
Glial cell line-derived neurotrophic factor (GDNF) plays key
roles in the control of vertebrate neuron survival and
differentiation. A novel neurotrophic factor was recently
cloned from human and mouse and designated neurturin (1,
2). Physiological responses to neurturin (NTN) require the
presence of receptor tyrosine kinase RET and a novel
glycosylphosphatidylinositol linked receptor NTNRα (3,4).
The cDNAs encoding NTNRα from human, rat, chicken, and
mouse have been cloned recently (3-8) and termed
GDNFRβ, Ret ligand 2 (RETL2) or TGF-β-related
neurotrophic factor receptor 2 (TrnR2) and nominated as
GFRα-2 recently (9). NTN binds to and forms a complex with
GFRα-2 and the Ret PTK and activates the RET receptor
tyrosine kinase pathway. Both NTN and GDNF can activate
the MAP kinase and phosphatidylinositol 3-kinase pathways
and play a critical role in the development of many neuronal
populations. Neurturin and GDNF define a new family of
neurotrophic factors.
SOURCE:
Rabbit anti-neurturin polyclonal antibody was raised against
a peptide corresponding to amino acids 178 to 193 of human
neurturin (1).
APPLICATION:
This polyclonal antibody can be used for detection of
neurturin by Western blot. An approximate 14 kDa band of
the full length recombinant NTN was detected. For research
use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at -20°C.
Stable for one year at 2-8°C.
Western blot analysis of NTN in
HeLa cell lyaste containing 10 or
2.5 ng of full length recombinant
NTN with anti-neurturin at 1:500.
REFERENCES:
1. Kotzbauer PT, Lampe PA, Heuckeroth RO, et al. Neurturin, a relative
glial-cell-line-derived neurotrophic factor. Nature 1996;384:467-470
2.
2. Heuckeroth RO, Kotzbauer P, Copeland NG, et al. Neurturin, a novel
neurotrophic factor, is localized to mouse chromosome 17 and human
chromosome 19p13.3. Genomics 1997;44(1):137-40
3. Klein RD, Sherman D, Ho WH, et al. GPI-linked protein that interacts with
Ret to form a candidate neurturin receptor. Nature 1997;387:717-721
4. Buj-Bello A, Adu J, Pinon LG, et al. Neurturin responsiveness requires a
GPI-linked receptor and the Ret receptor tyrosine kinase. Nature
1997;387:721-724
5. Baloh RH, Tansey MG, Golden JP, et al. TrnR2, a novel receptor that
mediates neurturin and GDNF signaling through Ret. Neuron 1997;18:793-
802
6. Sanicola M, Hession C, Worley D, et al. Glial cell line-derived neurotrophic
factor-dependent RET activation can be mediated by two different cellsurface
accessory proteins. Proc Natl Acad Sci USA 1997;94:6238-6243
7. Suvanto P, Wartiovaara K, Lindahl M, et al. Cloning, mRNA distribution
and chromosomal localisation of the gene for glial cell line-derived
neurotrophic factor receptor beta, a homologue to GDNFR-alpha. Hum Mol
Genet 1997;6:1267-1273
8. Wang CY, Ni J, Jiang H, et al. Cloning and characterization of glial cell
line-derived neurotrophic factor receptor-B: a novel receptor for members of
glial cell line-derived neurotrophic factor family of neurotrophic factors.
Neuroscience 1998;83(1):7-14
9. Nomenclature Committee. Nomenclature of GPI-linked receptors for the
GDNF ligand family. GFRα Neuron 1997;19:485 (RD0500)

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Anti-Eotaxin
CATALOG No.: 1123
BACKGROUND:
Chemokines play a key role in inflammation. The CC
chemokine eotaxin is a potent and specific eosinophil
chemoattractant that is expressed by a variety of cell types
in certain inflammatory conditions (1,2). Some G-protein
coupled chemokine receptors are also utilized as virus
coreceptors for fusion and infection of cells. The eotaxin
receptor CCR3 is required for HIV-1 entry into target cells
such as microglia and eotaxin inhibits the infection of HIV-1
(3,4).
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 1123P).
Western blot analysis of
eotaxin in HeLa cell lysate
containing 10, 2.5, or 1 ng of
full length recombinant
eotaxin with anti-eotaxin at 1
µg/ml.
SOURCE:
This polyclonal antibody was raised in rabbits against a
peptide corresponding to amino acids 83 to 97 of human
eotaxin (1,2).
APPLICATION:
This polyclonal antibody can be used for detection of eotaxin
by Western blot at 0.5 to 1 µg/ml. The recombinant protein
can be used as positive control and monomer and
homodimer are detected at approximate 9 and 18 kDa. For
research use only.
REFERENCES:
1. Kitaura M, Nakajima T, Imai T, et al. Molecular cloning of human
eotaxin, an eosinophil-selective CC chemokine, and identification
of a specific eosinophil eotaxin receptor, CC chemokine receptor 3.
J Biol Chem 1996;271:7725-30
2. Ponath PD, Qin S, Ringler DJ, et al. Cloning of the human
eosinophil chemoattractant, eotaxin. Expression, receptor binding,
and functional properties suggest a mechanism for the selective
recruitment of eosinophils. J Clin Invest 1996;97:604-12
3. He J, Chen Y, Farzan M, et al. CCR3 and CCR5 are coreceptors
for HIV-1 infection of microglia. Nature.
1997;385(6617):645-9
4. Choe H, Farzan M, Sun Y, et al. The beta-chemokine receptors
CCR3 and CCR5 facilitate infection by primary HIV -1 isolates. Cell.
1996;85:1135-48
(WD0500)
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.

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Anti-SIRPα (CT) SHPS-1, MyD-1, BIT, p84
CATALOG No.: 1125
BACKGROUND:
Protein tyrosine phosphatases (PTPases) SHP-1 and SHP-2
are critical regulators in the intracellular signaling pathways
that result in cell responses such as mitosis, differentiation,
migration, survival, transformation or death. SHP-2 is a
signal transducer for several receptor tyrosine kinases and
cytokine receptors. A novel SHP-2 associated glycoprotein
was recently cloned from human, rat, mouse and cattle by
several labs and was designated SIRPα (1), SHPS-1 (2,3),
MyD-1 (4), BIT (5,6) and p84 (7). SIRPα is a new gene
family containing at least fifteen members. SIRPα is a
substrate of many activated tyrosine kinases such as insulin
receptor, EGFR, PDGFR and src, and a specific docking
protein for SHP-2 (1,2,5,8). SIRPα has regulatory effects on
cellular responses induced by serum, growth factors, insulin,
oncogenes, growth hormones and cell adhesion and plays a
general role in different physiological and pathological
processes (1,2,5,8).
SOURCE:
Rabbit anti-SIRPα polyclonal antibody was raised against a
peptide corresponding to amino acids 487 to 503 of human
SIRPα1 (1). The sequences of immunogenic peptide differ
from those of mouse, rat and bovine by one amino acid (1-
7).
cells can be used as positive control and 75-110 kDa bands
should be detected. It is human, mouse, and rat reactive
and recognizes SIRPα1, 2 and 3. For research use only.
Western blot analysis of
SIRPα in THP-1 whole
cell lysate with anti-
SIRPα at 1:2000
dilution.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
REFERENCES:
1. Kharitonenkov A, et al. Nature 1997;386:181-186.
2. Fujioka Y, et al. Mol Cell Biol 1996;16:6887-6899
3. Yamao T, et al. Biochem Biophys Res Commun 1997;231:61-67
4. Brooke GP, et al. Eur J Immunol 1998;28:1-11
5. Ohnishi H, et al. J Biol Chem 1996;271:25569-25574
6. Ohnishi H, et al. Genomics 1997;40:504-506
7. Comu S, et al. J Neurosci 1997;17:8702-8710
8. Stofega MR, et al. J Biol Chem 1998;273:7112-7117
(RD1299)
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:1000 to 1:2000 dilution. Whole cell lysate from THP-1

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Anti-Caspase-10 (CT) FLICE2
CATALOG No.: 1128
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD)- containing
adapter molecules and members of the ICE/CED-3 protease
family. A novel ICE/CED-3 protease was identified recently,
designated FLICE2 and Mch4 1,2 and renamed as caspase-
10. Caspase-10 has two death effector domains (DEDs) that
bind to the DED in the adapter molecule FADD and recruits
both TNFR1 and CD95 to form complexes with these
receptors. Caspase-10 is therefore involved in the CD95 and
TNFR1 induced apoptosis 1 . Caspase-10 cleaves and
activates caspase-3, -4, -6, -7, -8 and -9, which causes the
proteolytic cleavage of many key proteins such as PARP.
Cleavage of PARP occurs in many different systems during
apoptosis and is the hallmark of programmed cell death 3 .
Caspase-10 is expressed in many tissues and cell lines 1,2 .
SOURCE:
Rabbit anti-caspase-10 polyclonal antibody was raised
against a peptide corresponding to amino acids 505 to 521
of human FLICE2 1 .
APPLICATION:
This polyclonal antibody can be used for detection of
caspase-10 by Western blot at 1:500 to 1:1000 dilution.
HeLa whole cell lysate can be used as positive control and a
59 kDa band can be detected. This antibody only recognizes
FLICE2 form of caspase-10. It is human, mouse and rat
reactive. For research use only.
Western blot analysis of
caspase-10 in HeLa (H), Jurkar
(J), A431 (A), K562 (K), and
NIH3T3 (3T3) whole cell
lysates with anti-caspase-10 at
1:1000 dilution.
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
REFERENCES:
1. Vincenz.C. and Dixit,V.M. Fas-associated death domain protein
interleukin-1beta-converting enzyme 2 (FLICE2), an ICE/Ced-3
homologue, is proximally involved in CD95- and p55-mediated
death signaling. J. Biol. Chem. 1997;272:6578-6583
2. Fernandes-Alnemri T, Armstrong RC, Krebs J, Srinivasula SM,
Wang L Bullrich F, Fritz LC, Trapani JA, Tomaselli KJ, Litwack G,
Alnemri ES. In vitro activation of CPP32 and Mch3 by Mch4, a
novel human apoptotic cysteine protease containing two FADD-like
domains. Proc. Natl. Acad. Sci. USA. 1996;93:7464-7469
3. Cohen GM. Caspases: the executioners of apoptosis. Biochem J
1997;326:1-16
(RD1299)

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Anti-NIK (CT)
CATALOG No.: 1129
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα, LPS
and mitogens. A serine/threonine protein kinase which
mediates NF-κB activation by IL-1, TNFα and CD95 was
identified recently and designated NIK (for NF-κB inducing
kinase) (1). NIK is an activator of IκB kinase alpha and beta
(IKKα and IKKβ) (2-5). Therefore, NIK is a key molecule in
the NF-κB signaling pathway leading to the induction of a
variety of gene expression in response to proinflammatory
cytokines and bacteria products.
SOURCE:
Rabbit anti-NIK polyclonal antibody was raised against a
peptide corresponding to amino acids 931 to 947 of human
NIK (1).
APPLICATION:
This polyclonal antibody can be used for detection of NIK by
Western blot. 293 cell lysate can be used as positive control.
STORAGE:
It is supplied as 100 µg purified IgG in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 1129P).
293 cell lysate, 200 µg/100 µl, is available for positive
control (Catalog No. 1210).
REFERENCES:
1. Malinin NL, Boldin MP, Kovalenko AV, Wallach . MAP3Krelated
kinase involved in NF-kappaB induction by TNF, CD95 and
IL-1. Nature 1997;385:540-544
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M.
Identification and characterization of an IkappaB kinase. Cell
1997;90:373-383
3. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DV. IkappaB
kinase-beta: NF-kappaB activation and complex formation with
IkappaB kinase-alpha and NIK. Science 1997;278:866-869
4. Ling L, Cao Z, Goeddel D. NF-kappaB -inducing kinase activates
IKK-alpha by phosphorylation of Ser-176. Proc Natl Acad Sci USA
1998;95:3792-3797
5. Nakano H, Shindo M, Sakon S, Nishinaka S, Mihara M, Yagita
H, Okumura K. Differential regulation of IkappaB kinase alpha and
beta by two upstream kinases, NF-kappaB-inducing kinase and
mitogen-activated protein kinase/ERK kinase kinase-1. Proc Natl
Acad Sci USA 1998;95:3537-3542 (RD0400)

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Anti-TACE (CT) ADAM17
CATALOG No.: 1131
BACKGROUND:
Tumor-necrosis factor-α is a proinflammatory cytokine and
contributes to a variety of inflammatory disease responses
and programmed cell death. TNF-α is synthesized as a 26K
type II membrane-bound precursor that is cleaved by a
convertase to generate secreted 17K mature TNF-α. TNF-α
converting enzyme (TACE) protein was recently purified and
the human and mouse TACE cDNAs were cloned by several
groups separately (1-3). TACE is a membrane-bound
metalloprotease-disintegrin in the family of mammalian
ADAM (for a disintegrin and metalloprotease). TACE also
processes other cell surface proteins, including TNF
receptor, TGFα, the L-selectin adhesion molecule, and
alpha-cleavage of amyloid protein precursor (APP) (4,5).
TACE mRNA is expressed in a variety of human and murine
tissues. TACE was selected as one of the few targets in
cytokine activation by the Eighth International Conference of
the Inflammation Research Association (6)
SOURCE:
Rabbit anti-TACE (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 807 to 823
of human TACE (1,2). This sequence differs from those of
mouse and rat TACE by one amino acid (3).
APPLICATION:
This polyclonal antibody can be used for detection of TACE
by Western blot at 1:500 to 1:2000 dilution. HeLa or Jurkat
whole cell lysate can be used as positive control and 80 to
130 kDa bands can be detected, which may represent
mature protein, precursor, and glycosylated TACE. It is
human, mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at -20°C, stable for one year.
Western blot analysis of
TACE in HeLa (1,3) and
Jurkat (2,4) whole cell lysate
in the absence (1,2) or
presence (3,4) of blocking
peptide (Catalog no. 1131P)
with anti-TACE (CT) at 1:500
dilution.
REFERENCES:
1. Black RA, Rauch CT, Kozlosky CJ, et al. A
metalloproteinase disintegrin that releases tumour-necrosis
factor-alpha from cells. Nature 1997;385:729-733
2. Moss ML, Jin SL, Milla ME, et al. Cloning of a disintegrin
metalloproteinase that processes precursor tumour-necrosis
factor-alpha. Nature 1997;385:733-736
3. Mizui Y, Yamazaki K, Sagane K, Tanaka I. cDNA cloning of
mouse tumor necrosis factor-alpha converting enzyme (TACE)
and partial analysis of its promoter. Gene 1999;233:67-74
4. Peschon JJ, Slack JL, Reddy P, et al. An essential role for
ectodomain shedding in mammalian development. Science
1998;282:1281-4
5. Buxbaum JD, Liu KN, Luo Y, et al. Evidence that tumor
necrosis factor alpha converting enzyme is involved in
regulated alpha-secretase cleavage of the Alzheimer amyloid
protein precursor. J Biol Chem 1998;273:27765-7
6. Giegel DA, Chaplin DD. Targets in cytokine activation.
Agents Actions Suppl 1998;49:1-3 (WD1299)

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Anti- GFRα-1 GDNFRα, RETL1, TrnR1
CATALOG No.: 1133
BACKGROUND:
Glial cell line-derived neurotrophic factor (GDNF) is a potent
survival factor for central and peripheral neurons and is
essential for the development of kidneys and the enteric
nerves system. Physiological responses to GDNF require
the presence of a novel glycosylphosphadidylinositol linked
protein GDNFRα, which is a cell surface receptor for GDNF
(1,2). The cDNAs encoding GDNFRα from human, rat,
chicken and mouse have been cloned recently (1-5).
GDNFRα was also termed Ret ligand 1 (RETL1) or TGF-βrelated
neurotrophic factor receptor 1 (TrnR1) and
nominated as GFRα-1 recently (5-7). GFRα-1 binds GDNF
specifically and mediates activation of the Ret protein
tyrosine kinase (PTK). Thus, GDNF, GFRα and the Ret PTK
form a complex to transduce GDNF signal and to mediate
GDNF function.
SOURCE:
Rabbit anti- GFRα-1 polyclonal antibody was raised against
a peptide corresponding to amino acids 369 to 382 of human
GFRα-1 (1).
APPLICATION:
This polyclonal antibody can be used for detection of GFRα-
1 by Western blot. The amino acid sequence of
immunogenic peptide is identical to those of mouse and rat
and the antibody recognizes GFRα-1 from human, mouse
and rat origins. This antibody is for research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
REFERENCES:
Western blot analysis of
GFRα-1 in crude
membrane fractions of
human brain (B), liver (L),
kidney (K), and spleen (S),
respectively, with anti-
GFRα−1 at 1:500 dilution.
1. Jing S; Wen D; Yu Y; Holst PL ; Luo Y; Fang M; Tamir R; Antonio L; Hu Z;
Cupples R; Louis JC; Hu S; Altrock BW; Fox GM. GDNF-induced activation
of the Ret protein tyrosien kinase is mediated by GDNFR-α, a novel receptor
for GDNF. Cell, 1996;85:1113-24.
2. Treanor JJS; GoodmanL; Sauvage FD; Stone DM; Poulsen KT; Beck CD;
Gray C; Armanini MP; Pollock RA; Herti F; Phillips HS; Goddard A; Moore
MW; Buj-Bello A;Davies AM; Asai N; Takahashi M; Vandlen R; Henderson
CE; Rosenthal A. Characterization of a multicomponent receptor for GDNF.
Nature, 1996;382:80-83.
3. Sanicola M, Hession C, Worley D, Carmillo P, Ehrenfels C, Walus L,
Robinson S, Jaworski G, Wei H, Tizard R, Whitty A, Pepinsky RB, Cate RL.
Glial cell line-derived neurotrophic factor-dependent RET activation can be
mediated by two different cell-surface accessory proteins. Proc Natl Acad
Sci U S. 1997;94:6238-6243
4. Buj-Bello A, Adu J, Pinon LG, Horton A, Thompson J, Rosenthal A,
Chinchetru M, Buchman VL, Davies AM. Neurturin responsiveness requires
a GPI-linked receptor and the Ret receptor tyrosine kinase. Nature
1997;387:721-724
5. Dey,B.K., Wong,Y.W. and Too,H.P. Cloning of a novel murine isoform of
the glial cell line-derived neurotrophic factor receptor. Neuroreport
1998;9:37-42
6. Baloh RH, Tansey MG, Golden JP, Creedon DJ, Heuckeroth RO, Keck
CL, ZimonjicDB, Popescu NC, Johnson EM Jr, Milbrandt J. TrnR2, a novel
receptor that mediates neurturin and GDNF signaling through Ret. Neuron
1997;18:793-802
7. Nomenclature Committee. Nomenclature of GPI-linked receptors for the
GDNF ligand family. GFRα.. Neuron 1997;19:485 (RD1299)

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Anti- GFRα−2, GDNFRβ, RETL2, TrnR2, NTNR-α
CATALOG No.: 1135
BACKGROUND:
Members of the glial cell line-derived neurotrophic factor
(GDNF) family, including GDNF and neurturin (NTN) (1),
play key roles in the control of vertebrate neuron survival
and differentiation. Physiological responses to NTN require
the presence of a novel glycosylphosphadidylinositol linked
protein NTNRα, which is a cell surface receptor for NTN
(2,3). The cDNAs encoding NTNRα from human, rat,
chicken, and mouse have been cloned recently (2-7).
NTNRα was also termed GDNFRβ, Ret ligand 2 (RETL2) or
TGF-β-related neurotrophic factor receptor 2 (TrnR2) (4-7)
and nominated as GFRα-2 recently (8). GFRα-2 binds NTN
and mediates activation of RET receptor tyrosine kinase by
both NTN and GDNF. Thus, NTN, GFRα-2, and the Ret PTK
form a complex to transduce NTN signal and to mediate
NTN function.
SOURCE:
Rabbit anti-GFRα-2 polyclonal antibody was raised against
a peptide corresponding to amino acids 377 to 391 of
human GFRα-2. The amino acid sequences of immunogenic
peptide are identical to those of mouse and rat.
APPLICATION:
This polyclonal antibody can be used for detection of GFRα-
2 by Western blot at 1:1000 to 1:2000 dilution. HeLa whole
cell lysate can be used as positive control and a 52 kDa
band should be detected. It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
REFERENCES:
Western blot analysis of GFRα-2
in HeLa total cell lysate with anti-
GFRα-2 at 1:1000 dilution.
1. Kotzbauer PT, Lampe PA, Heuckeroth RO, Golden JP, Creedon
DJ, Johnson EM Jr, lbrandt J. Neurturin, a relative glial-cell-linederived
neurotrophic factor. Nature 1996;384:467-470
2. Klein RD, Sherman D, Ho WH, Stone D, Bennett GL, Moffat B,
Vandlen R, Simmons L, Gu Q, Hongo JA, Devaux B, Poulsen K,
Armanini M, Nozaki C, Asai N, Goddard A, Phillips H, Henderson
CE, Takahashi M, Rosenthal A. A GPI-link ed protein that interacts
with Ret to form a candidate neurturin receptor. Nature
1997;387:717-721
3. Buj-Bello A, Adu J, Pinon LG, Horton A, Thompson J, Rosenthal
A, Chinchetru M, Buchman VL, Davies AM. Neurturin
responsiveness requires a GPI-linked receptor and the Ret receptor
tyrosine kinase. Nature 1997;387:721-724
4. Baloh RH, Tansey MG, Golden JP, Creedon DJ, Heuckeroth RO,
Keck CL, Zimonjic DB, Popescu NC, Johnson EM Jr, Milbrandt J.
TrnR2, a novel receptor that mediates neurturin and GDNF
signaling through Ret. Neuron 1997;18:793-802
5. Sanicola M, Hession C, Worley D, Carmillo P, Ehrenfels C,
Walus L, Robinson S, Jaworski G, Wei H, Tizard R, Whitty A,
Pepinsky RB, Cate RL. Glial cell line-derived neurotrophic factordependent
RET activation can be mediated by two different cellsurface
accessory proteins. Proc Natl Acad Sci USA 1997;94:6238-
6243
6. Suvanto P, Wartiovaara K, Lindahl M, Arumae U, Moshnyakov
M, Horelli-Kuitunen N, Airaksinen MS, Palotie A, Sariola H, Saarma
M. Cloning, mRNA distribution and chromosomal localisation of the
gene for glial cell line-derived neurotrophic factor receptor beta, a
homologue to GDNFR-alpha. Hum Mol Genet 1997;6:1267-1273
7. Wang CY, Ni J, Jiang H, Hsu TA, Dugich-Djordjevic M, Feng L,
Zhang M, Mei L, Gentz R, Lu B. Cloning and characterization of
glial cell line-derived neurotrophic factor receptor-B: a novel
receptor for members of glial cell line-derived neurotrophic factor
family of neurotrophic factors. Neuroscience 1998 Mar;83(1):7-14
8. Nomenclature Committee. Nomenclature of GPI-linked receptors
for the GDNF ligand family. GFRα. Neuron 1997;19:485 (RD1299)

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Anti- GFRα-3, GDNFRγ, RETL2, TrnR2, NTNR-α
CATALOG No.: 1137
BACKGROUND:
Members of the glial cell line-derived neurotrophic factor
(GDNF) family including GDNF and neurturin (NTN) play
essential roles in the control of vertebrate neuron survival
and differentiation. A new member of the GDNF family was
recently identified and designated persephin (1).
Physiological responses to these neurotrophic factors
require two receptor subunits, the novel
glycosylphosphadidylinositol linked protein GFRα and Ret
receptor tyrosine kinase GFRβ (2). Following the findings of
GFRα-1 and -2, a novel receptor in GFRα family was
identified very recently from human and mouse and
designated GFRα-3 (3-7). GFRα-3 binds persephin, thus,
persephin, GFRα-3, and Ret PTK form a complex to
transduce persephin signal and to mediate persephin
function.
SOURCE:
Rabbit anti-GFRα-3 polyclonal antibody was raised against
a peptide corresponding to amino acids from 347 to 360 of
murine GFRα-3 (6).
APPLICATION:
This polyclonal antibody can be used for detection of GFRα-
3 expression by Western blot at 1:500 to 1:1000 dilution.
Murine kidney, liver or heart tissue lysates can be used as
positive control. It is human mouse, and rat reactive. For
research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
REFERENCES:
Western blot analysis of
GFRα−3 in crude cell
membrane fractions of
murine heart (H), spleen
(S), kidney (K), liver (L),
and brain (B), respectively,
with anti-GFRα−3 at 1:500
dilution.
1. Milbrandt J, de Sauvage FJ, Fahrner TJ, et al. Persephin, a
novel neurotrophic factor related to GDNF and neurturin. Neuron
1998;20:245-253.
2. Nomeclature Committee. Nomeclature of GPI-linked receptors
for the GDNF ligand family. GFRα. Neuron 1997: 19:485.
3. Jing S. Yu Y, Fang M, Hu Z, Holst PL, Boone T, Delaney J.
Schultz H, Zhou R, Fox GM. GFRalpha-2 and GFRalpha-3 are two
new receptors for ligands of the DGNF family. J Biol Chem 1997;
272:33111-33117
4. Baloh RH, Gorodinsky A, Golden JP, Tansey MG, Keck CL,
Popescu NC, Johnson EM Jr, Milbrandt J. GFRalpha3 is an orphan
member of the GDNF/neurturin/persephin receptor family. Proc Natl
Acad Sci USA 1998;95:5801-5806.
5. Worby CA, Vega QC, Chao HH, Seasholtz AF, Thompson RC,
Dixon JE. Identification and characterization of GFRalpha-3, a
novel Co-receptor belonging to the glial cell line-derived
neurotrophic receptor family. J Biol Chem 1998;273:3502-3508.
6 Naveilhan P, Baudet C, Mikaels A, Shen L, Westphal H, Ernfors
P. Expression and regulation of GFRalpha3, a glial cell line-derived
neurotrophic factor family receptor. Proc Natl Acad Sci USA
1998;95:1295-1300.
7. Nomoto,S., Ito,S., Yang,L.X. and Kiuchi,K. Molecular cloning and
expression analysis of GFR alpha-3, a novel cDNA related to
GDNFR alpha and NTNR alpha. Biochem. Biophys. Res. Commun.
1998;244:849-853. (RD1299)

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Anti-DR4 (CT) TRAIL-R1
CATALOG No.: 1139
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand in the TNF family through their
death domain containing receptors, TNFR1 and Fas. A
novel death domain containing receptor was recently
identified and designated DR4 (for death receptor 4) 1 . The
ligand for this novel death receptor has been identified and
termed TRAIL 2,3 , which is a new member in the TNF family.
DR4 is also called TRAIL receptor-1 (TRAIL-R1) 4 . DR4 is
expressed in most of human tissues including spleen,
peripheral blood leukocytes, small intestine and thymus.
Like TNFR1, Fas and DR3, DR4 mediates apoptosis and
NF-κB activation in many tissues and cells.
SOURCE:
Rabbit anti-DR4 (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 427 to 445 of
human DR4 mature protein.
APPLICATION:
This polyclonal antibody can be used for detection of DR4
expression by Western blot at 1:500 to 1:1000 dilution. HeLa
whole cell lysate can be used as positive control and a 57
kDa band should be detected. It is human, mouse, and rat
reactive and has no cross reaction to DR5. For research use
only.
Western blot analysis of DR4
in HeLa total cell lysate with
anti-DR4 (CT) at 1:500
dilution.
REFERENCES:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R; Ebner
R; Ni J; Dixit VM. The receptor for the cytotoxic ligand TRAIL.
Science; 1997;276:111-113
2. Wiley SR, Schooley K, Smolak PJ, Din WS, Huang CP, Nicholl
JK, Sutherland GR, Smith TD, Rauch C, Smith CA, et al.
Identification and characterization of a new member of the TNF
family that induces apoptosis. Immunity 1995;3:673-682
3. Pitti RM; Marsters SA; Ruppert S; Donahue CJ; Moore A;
Ashkenazi A. Induction of apoptosis by Apo-2 ligand, a new member
of the tumor necrosis factor cytokine family. J. Biol. Chem.
1996;271:12687-90
4. Schneider P, Thome M, Burns K, Bodmer JL, Hofmann K,
Kataoka T, Holler N, Tschopp J. TRAIL receptors 1 (DR4) and 2
(DR5) signal FADD-dependent apoptosis and activate NF-κB.
Immunity 1997;7:831-836
(RD1299)
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.

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Anti-DFF45 (CT)
CATALOG No.: 1141
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A human 45 kDa
DNA fragmentation factor (DFF45) was identified recently
which was cleaved by caspase-3 during apoptosis (1).
Mouse homologue of human DFF45 was identified as a
DNase inhibitor designated ICAD (2,3). Upon cleavage of
DFF45/ICAD, a caspase activated deoxyribonuclease
(DFF40/CAD) is released and activated and eventually
causes the degradation of DNA in the nuclei (2-5).
Therefore, the cleavage of DFF45/ICAD, which causes
DFF40/CAD activation and DNA degradation, is the hallmark
of apoptotic cell death.
SOURCE:
Rabbit anti-DFF45 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 313 to 331
of human DFF45 (1).
APPLICATION:
This polyclonal antibody can be used for detection of DFF45
and one of the cleaved fragments of DFF45 by Western blot
(6) at 1:1000 to 1:2000 dilution and for immunoprecipitation.
HeLa whole cell lysate can be used as positive control and a
45 kDa band can be detected in non-apoptotic cells. For
research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of
DFF45 in HeLa (H), Jurkat
(J), A431 (A), and K562 (K)
whole cell lysate with anti-
DFF45 (CT) at 1:1000
dilution.
REFERENCES:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric protein
that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
2. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
3. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
4. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X. The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
5. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H,
Nagata S. Molecular cloning and characterization of human
caspase-activated DNase. Proc Natl Acad Sci USA 1998;95:9123-8
6. Tang D, Kidd VJ. Cleavage of DFF-45/ICAD by multiple
caspases is essential for its function during apoptosis. J Biol Chem
1998;273:28549-52
(RD1299)

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Anti-DFF45/35 (NT)
CATALOG No.: 1148
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A human 45 kDa
DNA fragmentation factor (DFF45) was identified recently
that was cleaved by caspase-3 during apoptosis (1). Mouse
homologue of human DFF45 was identified as a DNase
inhibitor designated ICAD (2,3). DFF45/ICAD have short
forms that were termed DFF35 and ICADs, respectively,
(2,4). Upon cleavage of DFF45/ICAD, the caspase activated
deoxyribonuclease (DFF40/CAD) is released and activated
and eventually causes the degradation of DNA in the nuclei
(2-5). Therefore, the cleavage of DFF45/ICAD, which causes
DFF40/CAD activation and DNA degradation, is the hallmark
of apoptotic cell death.
SOURCE:
Rabbit anti-DFF45 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 2 to 21 of
human DFF45 (1).
APPLICATION:
This polyclonal antibody can be used for detection of DFF45,
DFF35, and one the cleaved fragment by Western blot at
1:1000 to 1:2000 dilution and for immunohistochemistry.
Jurkat whole cell lysate can be used as positive control and
45 and 35 kDa bands can be detected in non-apoptotic cells.
For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of
DFF45/35 in HeLa, (H),
K562 (K), Jurkat (J), and
Raji (R) whole cell lysate
with anti-DFF45/35 (NT)
at 1:1000 dilution.
REFERENCES:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
2. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
3. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
4. Gu J, Dong RP, Zhang C, McLaughlin DF, Wu MX, Schlossman
SF. Functional interaction of DFF35 and DFF45 with caspaseactivated
DNA fragmentation nuclease DFF40. J Biol Chem
1999;274:20759-62
5. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X. The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
6. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H,
Nagata S. Molecular cloning + characterization of human caspaseactivated
DNase. Proc Natl Acad Sci USA 1998;95:9123-8
(RD1299)

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Anti-MADD DENN
CATALOG No.: 1150
BACKGROUND:
MAP kinase-activating death domain protein (MADD) was
initially identified as the type 1 tumor necrosis factor receptor
(TNFR1) associated protein though their death domains (1).
Overexpression of MADD activates MAP kinases ERK and
JNK and induces the phosphorylation of cytosolic
phospholipase A2 (1). MADD shares 98% identity with
DENN (for differentially expressed in neoplastic vs. normal
cells), which was recently identified as a substrate for c-jun
N-terminal kinase 3 (JNK3) (2, 3). MADD has greater than
94% overall identity to a GDP/GTP exchange protein Rab3-
GEP (4, 5). MADD is 87% identical to KIAA0358, a brain
protein of unknown function (4). Identification of MADD as a
component of the TNFR1 signaling complex and the
similarity between MADD and Rab3-GEP provides a
connection between TNFR1 activation and downstream
MAP kinase activity through a guanine-nucleotide exchange
protein.
SOURCE:
Rabbit anti-MADD polyclonal antibody was raised against a
peptide corresponding to amino acids 1570 to 1588 of
human MADD (1). The sequence of immunogenic peptide is
identical to that of DENN and differs by one amino acid with
rat GDP/GTP exchange protein Rab3-GEP (2,5).
APPLICATION:
This polyclonal antibody can be used for detection of MADD
by Western blot at 1:250 to 1:500 dilution. Whole cell lysate
from HeLa or NIH3T3 cells can be used as positive control
and 200 to 220 kDa bands should be detected. It is human
and mouse reactive. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
Western blot analysis
of MADD in whole cell
lysates from the
indicated cell lines with
anti-MADD at 1:250
dilution.
REFERENCES:
1. Schievella AR, Chen JH, Graham JR, Lin LL. MADD, a novel
death domain protein that interacts with the type 1 tumor necrosis
factor receptor and activates mitogen-activated protein kinase. J
Biol Chem 1997;272:12069-12075
2. Chow VT, Lee SS. DENN, a novel human gene differentially
expressed in normal and neoplastic cells. DNA Seq 1996;6:263-
273
3. Zhang Y, Zhou L, Miller CA. A splicing variant of a death
domain protein that is regulated by a mitogen-activated kinase is a
substrate for c-Jun N-terminal kinase in the human central nervous
system. Proc Natl Acad Sci U S A 1998;95:2586-2591
4. Brown TL and Howe PH. MADD is highly homologous to a Rab3
guanine-nucleotide exchange protein (Rab3-GEP). Curr Biol
1998;8:R191
5. Wada M, Nakanishi H, Satoh A, Hirano H, Obaishi H, Matsuura
Y, Takai Y. Isolation and characterization of a GDP/GTP exchange
protein specific for the Rab3 subfamily small G proteins. J Biol
Chem 1997;272:3875-3878.
(RD1299)

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Anti-ASK1 (CT) MAPKKK5
CATALOG No.: 1151
BACKGROUND:
Mitogen-activated protein (MAP) kinase cascades are
activated in response to various extracellular stimuli,
including cytokines, growth factors and environmental
stresses. A novel MAP kinase kinase kinase (MAPKKK) was
recently identified and designated ASK1 (for apoptosis
signal-regulating kinase 1) and MAPKKK5 (1-3). ASK1
activated two different subgroups of MAPKK, MKK4 and
MKK6, which in turn activated c-Jun N-terminal kinase (JNK)
and p38 MAP kinase, respectively. ASK1/MAPKKK5 is
activated by TNFR and Fas through the interaction with
members of the TRAF family and Fas-associated protein
Daxx. Overexpression of ASK1 induced apoptotic cell death,
and a catalytically inactive form of ASK1 inhibited TNF-αinduced
apoptosis. ASK1 is expressed in variety of human
and mouse tissues.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year
Western blot analysis of
ASK1 in SW1353 whole cell
lysate with anti-ASK1 at
1:500 dilution.
REFERENCES:
1. Ichijo H, Nishida E, Irie K, ten Dijke P, Saitoh M, Moriguchi T,
Takagi M, Matsumoto K, Miyazono K, Gotoh Y. Induction of
apoptosis by ASK1, a mammalian MAPKKK that activates
SAPK/JNK and p38 signaling pathways. Science 1997;275:90-4
SOURCE:
Rabbit anti-ASK1 polyclonal antibody was raised against a
peptide corresponding to amino acids 1356 to 1375 of
human ASK1 (1). This sequence is different from that of
mouse by last two amino acids (3).
APPLICATION:
This polyclonal antibody can be used for detection of ASK1
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from SW1353 can be used as positive control and a 155
kDa band can be detected. For research use only.
2. Wang XS, Diener K, Jannuzzi D, Trollinger D, Tan TH,
Lichenstein H, Zukowski M, Yao Z. Molecular cloning and
characterization of a novel protein kinase with a catalytic domain
homologous to mitogen-activated protein kinase kinase kinase. J
Biol Chem 1996;271:31607-11
3. Tobiume K, Inage T, Takeda K, Enomoto S, Miyazono K, Ichijo
H. Molecular cloning and characterization of the mouse apoptosis
signal-regulating kinase 1. Biochem Biophys Res Commun
1997;239:905-10
(RD1299)

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Anti-mFLIP (CT) CASHα
CATALOG No.: 1156
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD) containing
adapter molecules and members of the ICE/CED-3 protease
family. Caspases-8 (FLICE) and -10 (FLICE2) are two
pivotal members in the ICE/CED-3 protease family. FLICEinhibitory
proteins were identified in virus and human and
designated v-FLIPs and FLIP respectively (1,2). The human
FLIP was also cloned by several labs independently and
termed Casper, I-FLICE, FLAME-1, CASH, CLARP and
MRIT (3-8). FLIP contains two death effector domains
(DEDs) and a caspase-like domain. FLIP interacts with
adapter protein FADD and caspase-8 and –10, and potently
inhibits apoptosis induced by all known death receptors
CD95, DR3, TRAIL-R and TNFR1.
SOURCE:
Rabbit anti-mFLIP polyclonal antibody was raised against a
peptide corresponding to amino acids 449 to 465 of mouse
FLIP L /CASHα (2,6).
APPLICATION:
This polyclonal antibody can be used for the detection of
FLIP by Western blot at 1:500 to 1:1000 dilution. NIH/3T3
whole cell lysate can be used as positive control and a 55
kDa band can be detected. FLIP has short form (FLIP S ) and
long form (FLIP L ) and this antibody recognizes the FLIP L
only. This antibody is for research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at -20°C. Stable for
one year at 2-8°C.
Western blot analysis of mFLIP
in NIH/3T3 whole cell lysate
with anti-mFLIP (CT) at 1:500
dilution.
REFERENCES:
1. Thome M, Schneider P, Hofmann K, Fickenscher H, Meinl E, Neipel F,
Mattmann C, Burns K, Bodmer JL, Schroter M, Scaffidi C, Krammer PH,
Peter ME, Tschopp J. Viral FLICE-inhibitory proteins (FLIPs) prevent
apoptosis induced by death receptors. Nature 1997;386:517-521.
2. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V,
Bodmer JL, Schroter M, Burns K, Mattmann C, Rimoldi D, French LE,
Tschopp J. Inhibition of death receptor signals by cellular FLIP. Nature
1997;388:190-195.
3. Shu HB, Halpin DR, Goeddel DV. Casper is a FADD- and caspase-related
inducer of apoptosis. Immunity 1997;6:751-763.
4. Hu S, Vincenz C, Ni J, Gentz R, Dixit VM. I-FLICE, a novel inhibitor of
tumor necrosis factor receptor-1- and CD-95-induced apoptosis. J Biol Chem
1997;272:17255-17257.
5. Srinivasula SM, Ahmad M, Ottilie S, Bullrich F, Banks S, Wang Y,
Fernandes -Alnemri T, Croce CM, Litwack G, Tomaselli KJ, Armstrong RC,
Alnemri ES. FLAME-1, a novel FADD-like anti-apoptotic molecule that
regulates Fas/TNFR1-induced apoptosis. J Biol Chem 1997;272:18542-
18545.
6. Goltsev YV, Kovalenko AV, Arnold E, Varfolomeev EE, Brodianskii VM,
Wallach D. CASH, a novel caspase homologue with death effector domains.
J Biol Chem 1997;272:19641-19644.
7. Inohara N, Koseki T, Hu Y, Chen S, Nunez G. CLARP, a death effector
domain-containing protein interacts with caspase-8 and regulates apoptosis.
Proc Natl Acad Sci USA 1997;94:10717-10722.
8. Han DK, Chaudhary PM, Wright ME, Friedman C, Trask BJ, Riedel RT,
Baskin DG, Schwartz SM, Hood L. MRIT, a novel death-effector domaincontaining
protein, interacts with caspases and BclXL and initiates cell death.
Proc Natl Acad Sci USA 1997;94:11333-11338.
9. Wallach D. Apoptosis. Placing death under control. Nature 1997;388:123.
(RD1299)

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Anti-DR3 (ED) Wsl-1, Apo-3, TRAMP, LARD
CATALOG No.: 1158
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain containing receptors, TNFR1 and Fas. A
novel cell death receptor was recently identified by several
groups independently and designated DR3, Wsl-1, Apo-3,
TRAMP and LARD 1-5 . The ligand for this novel death
receptor has been defined as TWEAK, also termed Apo3L.
DR3 is highly expressed in the tissues enriched in
lymphocytes including PBL, thymus and spleen. Like
TNFR1, DR3 induces apoptosis and NF-κB activation.
SOURCE:
Rabbit anti-DR3 (ED) polyclonal antibody was raised against
a peptide corresponding to amino acids 59 to 77 in
extracellular domain (ED) of human DR3 precusor 1,2 .
APPLICATION:
This polyclonal antibody can be used for detection of DR3
expression by Western blot at 1:500 to 1:1000 dilution.
Jurkat total cell lysate can be used as positive control and a
59 kDa band should be detected. It is human and mouse
reactive. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of DR3
in Jurkat total cell lysate with
anti-DR3 (ED) at 1:1000
dilution.
REFERENCES:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan
DR; Xing L; Gentz R; Ni J; Dixit VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT;
Grinham CJ; Brown R; Farrow SN. Nature, 1996;384:372-5.
3. Marsters SA; Sheridan JP; Donahue CJ; Pitti RM; Gray CL;
Goddard AD; Bauer KD; Ashkenazi A. Curr Biol, 1996;6:1669-76.
4. Bodmer JL; Burns K; Schneider P; Hofmann K; Steiner V; Thome
M; Bornand T; Hahne M; Schroter M; Becker K; et al. Immunity,
1997;6:79-88.
5. Screaton GR; Xu XN; Olsen AL; Cowper AE; Tan R; McMichael
AJ; Bell JI. Proc. Nat. Acad. Sci. USA. 1997;94:4615-9.
(RD1299)

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Anti-FLIP (NT) Casper, I-FLICE, FLAME-1, CASH, CLARP
CATALOG No.: 1159
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD)- containing
adapter molecules and members of the ICE/CED-3 protease
family. Caspases-8 (FLICE) and -10 (FLICE2) are two
pivotal members in the ICE/CED-3 protease family. FLICEinhibitory
proteins were identified in virus and human and
designated v-FLIPs and FLIP, respectively 1,2 . The human
FLIP was also cloned by several labs independently and
termed Casper, I-FLICE, FLAME-1, CASH and CLARP 3-7 .
FLIP contains two death effector domains (DEDs) and a
caspase-like domain. FLIP interacts with adapter protein
FADD and caspase-8 and –10, and potently inhibits
apoptosis induced by all known death receptors. Four splice
variants of c-FLIPs have been identified and termed FLIPα,
β, γ, and δ, respectively 8 .
SOURCE:
Rabbit anti-FLIP (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 2 to 18 of
human FLIP 2 . The sequence is identical in all FLIP splice
variants.
APPLICATION:
This polyclonal antibody can be used for Western blot at
1:500 to 1:1000 dilution. It recognizes all FLIP splice
variants including FLIPα, β, γ, and δ and is human, mouse
and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
REFERENCES:
1. Thome M, Schneider P, Hofmann K, Fickenscher H, Meinl E,
Neipel F, Mattmann C, Burns K, Bodmer JL, Schroter M, Scaffidi C,
Krammer PH, Peter ME, Tschopp J. Viral FLICE-inhibitory proteins
(FLIPs) prevent apoptosis induced by death receptors. Nature
1997;386:517-521
2. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner
V, Bodmer JL, Schroter M, Burns K, Mattmann C, Rimoldi D,
French LE, Tschopp J. Inhibition of death receptor signals by
cellular FLIP. Nature 1997;388:190-195
3. Shu HB, Halpin DR, Goeddel DV. Casper is a FADD- and
caspase-related inducer of apoptosis. Immunity 1997;6:751-763
4. Hu S, Vincenz C, Ni J, Gentz R, Dixit VM. I-FLICE, a novel
inhibitor of tumor necrosis factor receptor-1- and CD-95-induced
apoptosis. J Biol Chem 1997;272:17255-17257
5. Srinivasula SM, Ahmad M, Ottilie S, Bullrich F, Banks S, Wang
Y, Fernandes-Alnemri T, Croce CM, Litwack G, Tomaselli KJ,
Armstrong RC, Alnemri ES. FLAME-1, a novel FADD-like antiapoptotic
molecule that regulates Fas/TNFR1-induced apoptosis. J
Biol Chem 1997;272:18542-18545
6. Goltsev YV, Kovalenko AV, Arnold E, Varfolomeev EE,
Brodianskii VM, Wallach D. CASH, a novel caspase homologue
with death effector domains. J Biol Chem 1997;272:19641-19644
7. Inohara N, Koseki T, Hu Y, Chen S, Nunez G. CLARP, a death
effector domain-containing protein interacts with caspase-8 and
regulates apoptosis. Proc Natl Acad Sci USA 1997;94:10717-10722
8. Wallach D. Apoptosis. Placing death under control. Nature
1997;388:123 (RD1299).

13100 Kirkham Way
Suite 207
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www.prosci-inc.com
Toll Free: 888-513-9525
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Fax: 858-513-2692
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Anti-FLIPα (CT) Casper, I-FLICE, FLAME-1, CASH, CLARP
CATALOG No.: 1161
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD)- containing
adapter molecules and members of the ICE/CED-3 protease
family. Caspases-8 (FLICE) and -10 (FLICE2) are two
pivotal members in the ICE/CED-3 protease family. FLICEinhibitory
proteins were identified in virus and human and
designated v-FLIPs and FLIP, respectively 1,2 . The human
FLIP was also cloned by several labs independently and
termed Casper, I-FLICE, FLAME-1, CASH and CLARP 3-7 .
FLIP contains two death effector domains (DEDs) and a
caspase-like domain. FLIP interacts with adapter protein
FADD and caspase-8 and –10, and potently inhibits
apoptosis induced by all known death receptors. Four splice
variants of c-FLIPs have been identified and termed FLIPα,
β, γ, and δ, respectively 8 .
SOURCE:
Rabbit anti-FLIP (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 447 to 464 at C-
terminus of human FLIPα/FLIP L form 2 .
APPLICATION:
This polyclonal antibody can be used for detection of FLIP
by Western blot at 1:500 to 1:2000 dilution. HeLa whole cell
lysate can be used as positive control and a 55 kDa band
can be detected. It is human, mouse and rat reactive. This
antibody recognizes the FLIPα only. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of
FLIP in HeLa (H), Jurkat (J),
and K562 (K) whole cell
lysate with anti-FLIP (CT) at
1:1000 dilution.
REFERENCES:
1. Thome M, Schneider P, Hofmann K, et al. Viral FLICE-inhibitory
proteins (FLIPs) prevent apoptosis induced by death receptors.
Nature 1997;386:517-521
2. Irmler M, Thome M, Hahne M, et al. Inhibition of death receptor
signals by cellular FLIP. Nature 1997;388:190-195
3. Shu HB, Halpin DR, Goeddel DV. Casper is a FADD- and
caspase-related inducer of apoptosis. Immunity 1997;6:751-763
4. Hu S, Vincenz C, Ni J, Gentz R, Dixit VM. I-FLICE, a novel
inhibitor of tumor necrosis factor receptor-1- and CD-95-induced
apoptosis. J Biol Chem 1997;272:17255-17257
5. Srinivasula SM, Ahmad M, Ottilie S, et al.. FLAME-1, a novel
FADD-like anti-apoptotic molecule that regulates Fas/TNFR1-
induced apoptosis. J Biol Chem 1997;272:18542-18545
6. Goltsev YV, Kovalenko AV, Arnold E, Varfolomeev EE,
Brodianskii VM, Wallach D. CASH, a novel caspase homologue
with death effector domains. J Biol Chem 1997;272:19641-19644
7. Inohara N, Koseki T, Hu Y, Chen S, Nunez G. CLARP, a death
effector domain-containing protein interacts with caspase-8 and
regulates apoptosis. Proc Natl Acad Sci USA 1997;94:10717-10722
8. Wallach D. Apoptosis. Placing death under control. Nature
1997;388:123 (RD1299)

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Anti-Daxx (CT)
CATALOG No.: 1163
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain containing receptors, TNFR1 and Fas. Cell
death signals are transduced by death domain (DD)-
containing adapter molecules and members of the ICE/CED-
3 protease family. A novel DD-containing molecule was
recently cloned from mouse, human and monkey and
designated Daxx 1,2 . Daxx binds specifically to the Fas death
domain and enhances Fas induced apoptosis and activates
the Jun N-terminal kinase (JNK) pathway. Daxx is widely
expressed in fetal and adult human and mouse tissues
indicating its important function in Fas signaling pathways 1,2 .
SOURCE:
Rabbit anti-Daxx (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 722 to 740
at C-terminus of human Daxx 1,2 .
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
APPLICATION:
This polyclonal antibody can be used for detection of Daxx
by Western blot at 1:500 to 1:1000 dilution. HeLa whole cell
lysate can be used as positive control and a 120 kDa major
band can be detected. The sequences of immunogenic
peptide are identical among human, monkey and mouse
origins of Daxx 1,2 , and the antibody recognizes Daxx from
all these species. For research use only.
Western blot analysis of Daxx in
HeLa total cell lysate with anti-
Daxx (CT) at 1:1000 dilution.
REFERENCES:
1. Yang X, Khosravi-Far R, Chang HY, Baltimore D. Daxx, a novel
Fas-binding protein that activates JNK and apoptosis. Cell
1997;89:1067-1076
2. Kiriakidou M, Driscoll DA, Lopez-Guisa JM, Strauss JF 3rd.
Cloning and expression of primate Daxx cDNAs and mapping of
the human gene to chromosome 6p21.3 in the MHC region. DNA
Cell Biol 1997;16:1289-1298
(RD1299)

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Anti-DR3 (NT) Wsl-1, Apo-3, TRAMP, LARD
CATALOG No.: 1166
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand of the TNF family through their
death domain containing receptors, TNFR1 and Fas. A novel
cell death receptor was recently identified by several groups
independently and designated DR3, Wsl-1, Apo-3, TRAMP
and LARD 1-5 . The ligand for this novel death receptor has
been defined as TWEAK, also termed Apo3L. DR3 is highly
expressed in the tissues enriched in lymphocytes including
PBL, thymus and spleen. Like TNFR1, DR3 induces
apoptosis and NF-κB activation.
SOURCE:
Rabbit anti-DR3 (NT) polyclonal antibody was raised against
a peptide corresponding to amino acids 25 to 40 of human
DR3 precusor 1,2 .
APPLICATION:
This polyclonal antibody can be used for detection of DR3 by
Western blot at 1:500 to 1:1000 dilution. Jurkat whole cell
lysate can be used as positive control and a 59 kDa band
can be detected. It is human and mouse reactive and has no
cross reaction to other death receptors. For research use
only.
STORAGE: It is supplied as purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis
of DR3 in Jurkat total
cell lysate with anti-
DR3 (NT) at 1:1000
dilution.
REFERENCES:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan
DR; Xing L; Gentz R; Ni J; Dixit VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT;
Grinham CJ; Brown R; Farrow SN. Nature, 1996;384:372-5.
3. Marsters SA; Sheridan JP; Donahue CJ; Pitti RM; Gray CL;
Goddard AD; Bauer KD; Ashkenazi A. Curr Biol, 1996;6:1669-76.
4. Bodmer JL; Burns K; Schneider P; Hofmann K; Steiner V;
Thome M; Bornand T; Hahne M; Schroter M; Becker K; et al.
Immunity, 1997;6:79-88.
5. Screaton GR; Xu XN; Olsen AL; Cowper AE; Tan R; McMichael
AJ; Bell JI. Proc. Nat. Acad. Sci. USA. 1997;94:4615-9.
(RD1299)

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Anti-DR4 (NT) TRAIL-R1
CATALOG No.: 1167
BACKGROUND:
Apoptosis, or programmed cell death, occurs during normal
cellular differentiation and development of multicellular
organisms. Apoptosis is induced by certain cytokines
including TNF and Fas ligand in the TNF family through their
death domain containing receptors, TNFR1 and Fas. A novel
death domain containing receptor was recently identified and
designated DR4 (for death receptor 4) 1 . The ligand for this
novel death receptor has been identified and termed
TRAIL 2,3 , which is a new member in the TNF family. DR4 is
also called TRAIL receptor-1 (TRAIL-R1) 4 . DR4 is expressed
in most of human tissues including spleen, peripheral blood
leukocytes, small intestine and thymus. Like TNFR1, Fas
and DR3, DR4 mediates apoptosis and NF-κB activation in
many tissues and cells.
SOURCE:
Rabbit anti-DR4 (NT) polyclonal antibody was raised against
a peptide corresponding to amino acid 1 to 20 of human
DR4 mature protein.
STORAGE:
Supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of DR4
in HeLa (H), K562 (K), and
Jurkat (J) whole cell lysate
with anti-DR4 (NT) at 1:500
dilution.
REFERENCES:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R; Ebner R; Ni J;
Dixit VM. The receptor for the cytotoxic ligand TRAIL. Science;
1997;276:111-113
2. Wiley SR, Schooley K, Smolak PJ, Din WS, Huang CP, Nicholl JK,
Sutherland GR, Smith TD, Rauch C, Smith CA, et al. Identification and
characterization of a new member of the TNF family that induces apoptosis.
Immunity 1995;3:673-682
APPLICATION:
This polyclonal antibody can be used for detection of DR4 by
Western blot at 1:500 to 1:1000 dilution. HeLa or Jurkat
whole cell lysate can be used as positive control and a 57
kDa band can be detected. For research use only.
3. Pitti RM; Marsters SA; Ruppert S; Donahue CJ; Moore A; Ashkenazi A.
Induction of apoptosis by Apo-2 ligand, a new member of the tumor necrosis
factor cytokine family. J. Biol. Chem. 1996;271:12687-90
4. Schneider P, Thome M, Burns K, Bodmer JL, Hofmann K, Kataoka T,
Holler N, Tschopp J. TRAIL receptors 1 (DR4) and 2 (DR5) signal FADDdependent
apoptosis and activate NF-κB. Immunity 1997;7:831-836
(RD1299)

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Anti-Bonzo (CT) STRL33, TYMSTR
CATALOG NO.: 1170
BACKGROUND:
Human immunodeficiency virus (HIV) and simian
immunodeficiency virus (SIV) require coreceptors, in addition
to CD4, to infect target cells. Some G protein-coupled
receptors including CCR5, CXCR4, CCR3, and CCR2b in
the chemokine receptor family have been identified as HIV
coreceptors. An orphan G protein-coupled receptor was
recently cloned and designated Bonzo, STRL33 and
TYMSTR, and identified as HIV and SIV coreceptor (1-4).
Bonzo/STRL33 is used by SIV, HIV-2 and HIV-1. The
messenger RNA of Bonzo/STRL33 is expressed in lymphoid
tissues and activated peripheral blood lymphocytes.
SOURCE:
Rabbit anti-Bonzo polyclonal antibody was raised against a
peptide corresponding to amino acids 319 to 338 of human
origin (1,2). The sequence of this peptide is identical to those
of macaque and African green monkey.
APPLICATION:
This polyclonal antibody can be used for detection of Bonzo
by Western blot at 1:1000 dilution. Whole cell lysate from
SW1353 cells can be used as positive control. This antibody
is for research use only.
STORAGE:
It is supplied as purified IgG fraction, 100 µg in 200 µl of
PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis of
Bonzo in SW1353 total
cells lysate with anti-
Bonzo (CT) at 1:1000
dilution.
REFERENCES:
1. Deng HK, Unutmaz D, KewalRamani VN, Littman DR.
Expression cloning of new receptors used by simian and human
immunodeficiency viruses. Nature 1997;388:296-300
2. Liao F, Alkhatib G, Peden KW, Sharma G, Berger EA, Farber
JM. STRL33, A novel chemokine receptor-like protein, functions as
a fusion cofactor for both macrophage-tropic and T cell line-tropic
HIV-1. J Exp Med 1997;185:2015-23
3. Alkhatib G, Liao F, Berger EA, Farber JM, Peden KW. A new
SIV co-receptor, STRL33. Nature 1997;388:238
4. Loetscher M, Amara A, Oberlin E, Brass N, Legler D, Loetscher
P, D'Apuzzo M, Meese E, Rousset D, Virelizier JL, Baggiolini M,
Arenzana-Seisdedos F, Moser B. TYMSTR, a putative chemokine
receptor selectively expressed in activated T cells, exhibits HIV -1
coreceptor function. Curr Biol 1997;7:652-60 (RD1299)

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Anti-ICAD (NT)
CATALOG No.: 2001
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A human DNA
fragmentation factor (DFF) was identified recently which is
cleaved by caspase-3 during apoptosis (1). Mouse
homologue of human DFF was identified as a DNase
inhibitor designated ICAD, for inhibitor of caspase-activated
DNase (2,3). Upon cleavage of DFF/ICAD, a caspase
activated deoxyribonuclease (CAD) is released and
activated and eventually causes the degradation of DNA in
the nuclei (2,3). Therefore, the cleavage of CAD inhibitor
molecule DFF/ICAD, which causes DNase activation and
DNA degradation, is the hallmark of apoptotic cell death (4).
SOURCE:
Rabbit anti-ICAD (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 2 to 21 of
mouse ICAD (2).
APPLICATION:
This polyclonal antibody can be used for detection of of
ICAD by Western blot at 1:500 to 1:1000 dilution. Murine
lung tissue lysate can be used as positive control and a 45
kDa band cad be detected. This antibody is for research use
only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis of
ICAD in murine lung
tissue lysate with anti-
ICAD (NT) at 1:500
dilution.
REFERENCES:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
2. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
3. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
4. Wyllie A. Apoptosis. An endonuclease at last. Nature
1998;39120-21(RD1299)

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Anti-ICAD (CT)
CATALOG No.: 2003
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A human DNA
fragmentation factor (DFF) was identified recently which was
cleaved by caspase-3 during apoptosis (1). Mouse
homologue of human DFF was identified as a DNase
inhibitor designated ICAD, for inhibitor of caspase-activated
DNase (2,3). Upon cleavage of DFF/ICAD, a caspase
activated deoxyribonuclease (CAD) is released and
activated and eventually causes the degradation of DNA in
the nuclei (2,3). Therefore, the cleavage of CAD inhibitor
molecule DFF/ICAD, which causes DNase activation and
DNA degradation, is the hallmark of apoptotic cell death (4).
SOURCE:
Rabbit anti-ICAD (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 312 to 331
of mouse ICAD (2).
APPLICATION:
This polyclonal antibody can be used for detection of ICAD
by Western blot at 1:500 to 1:2000 dilution. Murine lung
tissue lysate can be used as positive control and a 45 kDa
band can be detected. This antibody is for research use
only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis
of ICAD in murine lung
(L), brain (B), liver (L),
and kidney tissue
lysate with anti-ICAD
(CT) at 1:1000 dilution.
REFERENCES:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
2. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
3. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
4. Wyllie A. Apoptosis. An endonuclease at last. Nature
1998;39120-21
(RD1299)

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Anti-CAD (I17)
CATALOG No.: 2007
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A mouse DNase
that causes DNA fragmentation was identified recently and
designated CAD (for caspase activated deoxyribonuclease)
(1,2). The human homologue of mouse CAD was more
recently identified by two groups independently and termed
CPAN and DFF40 (3,4). Human DFF45 and its mouse
homologue ICAD are the inhibitors of CPAN/DFF40 and
CAD, respectively (5). Upon cleavage of DFF45/ICAD by
activated caspase, DFF40/CAD is released and activated
and eventually causes the degradation of DNA in the nuclei
(1-4). Activation of CAD/DFF40, which causes DNA
degradation, is the hallmark of apoptotic cell death.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis of
CAD in murine kidney
tissue lysate with anti-CAD
(I17) at 1:500 dilution.
REFERENCES:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
2. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
3. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
SOURCE:
Rabbit anti-CAD (I17) polyclonal antibody was raised against
a peptide corresponding to amino acids 205 to 222 of murine
CAD (1).
APPLICATION:
This polyclonal antibody can be used for detection of CAD
by Western blot at 1:500 to 1:1000 dilution. Murine kidney
tissue lysate can be used as positive control and a 40 kDa
band should be detected. It is mouse and rat reactive. For
research use only.
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
4. Halenbeck R, MacDonald H, Roulston A, Chen TT, Conroy L,
Williams LT. CPAN, a human nuclease regulated by the caspasesensitive
inhibitor DFF45. Curr Biol 1998;8:537-40
5. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
(RD1299)

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Anti-CAD (CT)
CATALOG No.: 2011
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A mouse DNase
that causes DNA fragmentation was identified recently and
designated CAD (for caspase activated deoxyribonuclease)
(1,2). The human homologue of mouse CAD was more
recently identified by two groups independently and termed
CPAN and DFF40 (3,4). Human DFF45 and its mouse
homologue ICAD are the inhibitors of CPAN/DFF40 and
CAD, respectively (1, 2, 5). Upon cleavage of DFF45/ICAD
by activated caspase, DFF40/CAD is released and activated
and eventually causes the degradation of DNA in the nuclei
(1-4). Activation of CAD/DFF40, which causes DNA
degradation, is the hallmark of apoptotic cell death.
SOURCE:
Rabbit anti-CAD (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 314 to 329 of murine
CAD (1).
APPLICATION:
This polyclonal antibody can be used for detection of CAD
by Western blot at 1:500 to 1:1000 dilution. Tissue lysate
from murine lung or kidney can be used as positive control
and a 40 kDa band should be detected. For research use
only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis of
CAD in murine lung (L) and
kidney (K) tissue lysates
with anti-CAD (CT) at 1:500
dilution.
REFERENCES:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
2. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
3. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
4. Halenbeck R, MacDonald H, Roulston A, Chen TT, Conroy L,
Williams LT. CPAN, a human nuclease regulated by the caspasesensitive
inhibitor DFF45. Curr Biol 1998;8:537-40
5. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
(RD1299)

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Anti-Apaf-1 (NT)
CATALOG No.: 2013
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
The mammalian homologues of the key cell death gene
CED-4 in C. elegans has been identified recently from
human and mouse and designated Apaf-1 (for apoptosis
protease-activating factor 1) (1,2). Apaf-1 binds to
cytochrome c (Apaf-2) and caspase-9 (Apaf-3), which leads
to caspase-9 activation. Activated caspase-9 in turn cleaves
and activates caspase-3 that is one of the key proteases,
being responsible for the proteolytic cleavage of many key
proteins in apoptosis (3). Apaf-1 can also associate with
caspase-4 and caspase-8 (4). Apaf-1 is ubiquitously
expressed in human tissues (1).
SOURCE:
Rabbit anti-Apaf-1 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 12 to 28 of
human Apaf-1 (1). The sequences of the immunogenic
peptide are identical between human and mouse (1,2)
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
REFERENCES:
1. Zou H, Henzel WJ, Liu X, Lutschg A, Wang X. Apaf-1, a human
protein homologous to C. elegans CED-4, participates in
cytochrome c-dependent activation of caspase-3. Cell
1997;90:405-13
2. Cecconi F, Alvarez-Bolado G, Meyer BI, Roth KA, Gruss P.
Apaf1 (CED-4 homolog) regulates programmed cell death in
mammalian development. Cell 1998;94:727-37
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M,
Alnemri ES, Wang X. Cytochrome c and dATP-dependent
formation ofApaf-1/caspase-9 complex initiates an apoptotic
protease cascade. Cell 1997;91:479-89
4. Hu Y, Benedict MA, Wu D, Inohara N, Nunez G. Bcl-XL interacts
with Apaf-1 and inhibits Apaf-1-dependent caspase-9 activation.
Proc Natl Acad Sci USA 1998;95:4386-91 (RD1299)
APPLICATION:
This polyclonal antibody can be used for detection of Apaf-1
by Western blot at 1:1000 to 1:2000 dilution. Whole cell
lysate from HeLa cells can be used as positive control and a
130 kDa band should be detected. It is human, mouse, and
rat reactive. This antibody is for research use only.

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Anti-Apaf1 (CT)
CATALOG No.: 2015
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
The mammalian homologous of the key cell death gene
CED-4 in C. elegans was identified recently from human and
mouse and designated Apaf1 for apoptosis proteaseactivating
factor 1 (1,2). Apaf1 binds to cytochrome c (Apaf2)
and caspase-9 (Apaf3), which leads to caspase-9 activation.
Activated caspase-9 in turn cleaves and activates caspase-3
that is one of the key proteases, being responsible for the
proteolytic cleavage of many key proteins in apoptosis (3).
Apaf1 can also associate with caspase-4 and caspase-8 (4).
Apaf1 transcript is ubiquitously expressed in human tissues
(1).
SOURCE:
Rabbit anti-Apaf1 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 1158 to
1177 of human Apaf1 (1). The sequence of the immunogenic
peptide differs from that of murine Apaf1 by one amino acid
(1,2)
APPLICATION:
This polyclonal antibody can be used for detection of Apaf1
by Western blot at 1:500 to 1:2000 dilution. Human heart
tissue lysate can be used as positive control and a 130 kDa
band should be detected. It is human, mouse and rat
reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
Apaf1 in human heart
tissue lysate with anti-Apaf1
(2015) at 1:500 dilution in
the absence (A) or
presence (B) of blocking
peptide.
REFERENCES:
1. Zou H, Henzel WJ, Liu X, Lutschg A, Wang X. Apaf-1, a human
protein homologous to C. elegans CED-4, participates in
cytochrome c-dependent activation of caspase-3. Cell
1997;90:405-13
2. Cecconi F, Alvarez-Bolado G, Meyer BI, Roth KA, Gruss P.
Apaf1 (CED-4 homolog) regulates programmed cell death in
mammalian development. Cell 1998;94:727-37
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M,
Alnemri ES, Wang X. Cytochrome c and dATP-dependent
formation of Apaf-1/caspase-9 complex initiates an apoptotic
protease cascade. Cell 1997;91:479-89
4. Hu Y, Benedict MA, Wu D, Inohara N, Nunez G. Bcl-XL interacts
with Apaf-1 and inhibits Apaf-1-dependent caspase-9 activation.
Proc Natl Acad Sci USA 1998;95:4386-91
(WD1299)
RELATED PRODUCTS:
Blocking peptide, 50 µg / 250 µl, is available for competition
studies (Catalog No. 2015P).

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Anti-DR5 Apo2, TRAIL-R2, TRICK2, KILLER
CATALOG No.: 2019
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand in the TNF family through their death domain
containing receptors. TRAIL/Apo2L is a new member of the
TNF family. DR4 was recently identified as the receptor for
TRAIL. A novel death domain containing receptor for TRAIL
was more recently identified and designated DR5, Apo2,
TRAIL-R2, TRICK2, or KILLER by several groups
independently (1-7). Like DR4, DR5 transcript is widely
expressed in normal tissues and in many types of tumor
cells. DR5 binds to TRAIL and mediates TRAIL induced cell
death. Overexpression of DR5 induces apoptosis and
activates NF-κB.
SOURCE:
Rabbit anti-DR5 polyclonal antibody was raised against a
peptide corresponding to amino acids 388 to 407 of human
DR5 precursor (1,2).
APPLICATION:
This polyclonal antibody can be used for detection of DR5
expression by Western blot at 1:500 to 1:1000 dilution.
Whole cell lysate from HeLa cells can be used as positive
control. It is human and mouse reactive and has no cross
reaction to DR4. For research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100 µg
in 200 µl of PBS containing 0.02% sodium azide. Store at -
20°C. Stable for one year at 2-8°C.
Western blot analysis of DR5
in HeLa (H) and K562 (K)
whole cell lysates with anti-
DR5 at 1:500 dilution.
2. Sheridan JP, Marsters SA, Pitti RM, Gurney A, Skubatch M,
Baldwin D, Ramakrishnan L, Gray CL, Baker K, Wood WI,
Goddard AD, Godowski P, Ashkenazi A. Control of TRAIL-induced
apoptosis by a family of signaling and decoy receptors. Science
1997;277:818-21
3. Walczak H, Degli-Esposti MA, Johnson RS, Smolak PJ, Waugh
JY, Boiani N, Timour MS, Gerhart MJ, Schooley KA, Smith CA,
Goodwin RG, Rauch CT. TRAIL-R2: a novel apoptosis-mediating
receptor for TRAIL. EMBO J 1997;16:5386-97
4. MacFarlane M, Ahmad M, Srinivasula SM, Fernandes-Alnemri
T, Cohen GM, Alnemri ES. Identification and molecular cloning of
two novel receptors for the cytotoxic ligand TRA IL. J Biol Chem
1997;272:25417-20
5. Screaton GR, Mongkolsapaya J, Xu XN, Cowper AE, McMichael
AJ, Bell JI. TRICK2, a new alternatively spliced receptor that
transduces the cytotoxic signal from TRAIL. Curr Biol 1997;7:693-6
6. Wu GS, Burns TF, McDonald ER 3rd, Jiang W, Meng R, Krantz
ID, Kao G, Gan DD, Zhou JY, Muschel R, Hamilton SR, Spinner
NB, Markowitz S, Wu G, el-Deiry WS. KILLER/DR5 is a DNA
damage-inducible p53-regulated death receptor gene. Nat Genet
1997;17:141-3
7. Chaudhary PM, Eby M, Jasmin A, Bookwalter A, Murray J, Hood
L Death receptor 5, a new member of the TNFR family, and DR4
induce FADD-dependent apoptosis and activate the NF-kappaB
pathway. Immunity 1997;7:821-30 (RD1299)
REFERENCES:
1. Pan G, Ni J, Wei YF, Yu G, Gentz R, Dixit VM. An antagonist
decoy receptor and a death domain-containing receptor for TRAIL.
Science 1997;277:815-8

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Anti-DcR2 (ID) TRAIL-R4, TRUNDD
CATALOG No.: 2021
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand in the TNF family through their death domain
containing receptors. TRAIL/Apo2L is a new member of the
TNF family and induces apoptosis of a variety of tumor cell
lines. DR4 and DR5 are the recently identified functional
receptors for TRAIL, and DcR1/TRID is a decoy receptor (1-
3). Another member of the TRAIL receptor family was more
recently identified and designated DcR2, TRAIL-R4, or
TRUNDD (4-6). DcR2 has an extracellular TRAIL-binding
domain but lacks intracellular death domain and does not
induce apoptosis. Like DR4 and DR5, DcR2 transcript is
widely expressed in normal human tissues. Overexpression
of DcR2 attenuated TRAIL-induced apoptosis.
SOURCE:
Rabbit anti-DcR2 (ID) polyclonal antibody was raised against
a peptide corresponding to amino acids 249 to 263 of human
DcR2 precursor (4-6).
APPLICATION:
This polyclonal antibody can be used for detection of DcR2
expression by Western blot at 1:1000 to 1:2000 dilution.
Whole cell lysate from HeLa cells can be used as positive
control. It is human, mouse, and rat reactive. For research
use only.
Western blot analysis of
DcR2 in HeLa whole cell
lysate with anti-DcR2 (ID)
at 1:1000 dilution.
REFERENCES:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R;
Ebner R; Ni J; Dixit VM. The receptor for the cytotoxic ligand
TRAIL. Science; 1997;276:111-113
2. Pan G, Ni J, Wei YF, Yu G, Gentz R, Dixit VM. An antagonist
decoy receptor and a death domain-containing receptor for TRAIL.
Science 1997;277:815-8
3. Sheridan JP, Marsters SA, Pitti RM, Gurney A, Skubatch M,
Baldwin D, Ramakrishnan L, Gray CL, Baker K, Wood WI,
Goddard AD, Godowski P, Ashkenazi A. Control of TRAIL-induced
apoptosis by a family of signaling and decoy receptors. Science
1997;277:818-21
4. Marsters SA, Sheridan JP, Pitti RM, Huang A, Skubatch M,
Baldwin D, Yuan J, Gurney A, Goddard AD, Godowski P,
Ashkenazi A. A novel receptor for Apo2L/TRAIL contains a
truncated death domain. Curr Biol 1997;7:1003-6
5. Degli-Esposti MA, Dougall WC, Smolak PJ, Waugh JY, Smith
CA, Goodwin RG. The novel receptor TRAIL-R4 induces NFkappaB
and protects against TRAIL-mediated apoptosis, yet
retains an incomplete death domain. Immunity 1997;7:813-20
STORAGE:
It is supplied as affinity chromatography purified IgG, 100 µg
in 200 µl of PBS containing 0.02% sodium azide. Store at -
20°C. Stable for one year at 2-8°C.
6. Pan G, Ni J, Yu G, Wei YF, Dixit VM. TRUNDD, a new member
of the TRAIL receptor family that antagonizes TRAIL signalling.
FEBS Lett 1998;424:41-5
(RD1299)

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Anti-IKKα (C1)
CATALOG No.: 2025
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα, and
bacteria product LPS. NF-κB is associated with IκB proteins
in the cell cytoplasm, which inhibit NF-κB activity. The longsought
IκB kinase (IKK), which phosphorylates IκB, and
mediates IκB degradation and NF-κB activation, was
recently identified by several laboratories (1-5). IKK is a
serine protein kinase, and the IKK complex contains alpha
and beta subunits (IKKα and IKKβ). IKKα and IKKβ interact
with each other and both are essential for the NF-κB
activation. IKKα specifically phosphorylates IκB-α. IKKα is
expressed in variety of human tissues.
SOURCE:
Rabbit anti-IKKα (C1) polyclonal antibody was raised against
a peptide corresponding to amino acids 716 to 734 of human
IKKα (1,2), which differs from corresponding murine
sequence by four amino acids.
APPLICATION:
This polyclonal antibody can be used for detection of IKKα
by Western blot at 1:1000 to 1:2000 dilution. Whole cell
lysate from HeLa or Jurkat cells can be used as positive
control and an 85 kDa band should be detected. It has no
cross response to IKKβ or IKKγ. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of IKKα
in HeLa whole cell lysate with
anti-IKKα (C1) at 1:1000
dilution.
REFERENCES:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A
cytokine-responsive IkappaB kinase that activates the transcription
factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M.
Identification and characterization of an IkappaB kinase. Cell
1997;90:373-83
3. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The
IkappaB kinase complex (IKK) contains two kinase subunits,
IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and
NF-kappaB activation. Cell 1997;91:243-52
4. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DY. IkappaB
kinase-beta: NF-kappaB activation and complex formation with
IkappaB kinase-alpha and NIK. Science 1997;278:866-9
5. Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J,
Young DB, Barbosa M, Mann M, Manning A, Rao A. IKK-1 and
IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB
activation. Science 1997; 278:860-6 (RD1299)

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Anti-ADAM10 (CT) KUZ, MADM
CATALOG No.: 2051
BACKGROUND:
Proinflammatory cytokine tumor necrosis factor-α (TNF-α)
contributes to a variety of inflammatory responses and
programmed cell death. Notch receptor and its ligand
participate in cell fate decisions during vertebrate
development and are associated with several human
disorders, including a T-cell lymphoma. TNF-α, notch and its
ligand delta are all membrane-bond molecules, which are
cleaved by proteases to release mature proteins or
functional receptor. ADAM10, a metalloprotease-disintegrin
in the family of mammalian ADAM (for a disintegrin and
metalloprotease), was recently identified to cleave TNF-α,
notch and its ligand delta (1-3). The genes encoding human,
mouse, and bovine ADAM10 were recently cloned and
designated ADAM 10, kuzbanian (KUZ), and MADM,
respectively, (1,2,4). ADAM10 mRNA is expressed in a
variety of human and bovine tissues (1,4).
SOURCE:
Rabbit anti-ADAM10 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 732 to 748
of human ADAM10 (1). This sequence is identical to those of
bovine and rat origins and differs from that of mouse
ADAM10 by one amino acid (2,4).
APPLICATION:
This polyclonal antibody can be used for detection of
ADAM10 by Western blot at 1:500 to 1:2000 dilution. Jurkat
whole cell lysate can be used as positive control and an
approximately 85 kDa band can be detected, which may
represent precursor. A 60 kDa faint band was detected in
some cell lines including Jurkat, which appears to be the
processed mature protein. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at -20°C, stable for one year.
REFERENCES:
Western blot analysis of
ADAM10 in Jurkat whole cell
lysate in the absence (1) or
presence (2) of blocking
peptide (Catalog no. 2051P)
with anti-ADAM10 (CT) at
1:1000 dilution.
1. Rosendahl MS, Ko SC, Long DL, et al. Identification and
characterization of a pro-tumor necrosis factor-alpha-processing
enzyme from the ADAM family of zinc metalloproteases. J Biol
Chem 1997;272:24588-93
2. Pan D, Rubin GM. Kuzbanian controls proteolytic processing of
Notch and mediates lateral inhibition during Drosophila and
vertebrate neurogenesis. Cell 1997;90:271-80
3. Qi H, Rand MD, Wu X, Sestan N, Wang W, Rakic P, Xu T,
Artavanis-Tsakonas S. Processing of the notch ligand delta by the
metalloprotease Kuzbanian. Science 1999;283:91-4
4. Howard L, Lu X, Mitchell S, Griffiths S, Glynn P. Molecular
cloning of MADM: a catalytically active mammalian disintegrinmetalloprotease
expressed in various cell types. Biochem J
1996;317:45-50
(RD1299)

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Anti-FLIP γ/δ (CT) FLIP, I-FLICE, FLAME-1, CASH, CLARP
CATALOG No.: 2055
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD)-containing
adapter molecules and members of the ICE/CED-3 protease
family. Caspases-8 (FLICE) and -10 (FLICE2) are two
pivotal members in the ICE/CED-3 protease family. FLICEinhibitory
proteins were identified in virus and human and
designated v-FLIPs and c-FLIPs, respectively 1,2 . The human
FLIPs were also cloned by several labs independently and
termed Casper, I-FLICE, FLAME-1, CASH, CLARP and
usurpin 3-7 . FLIP contains two death effector domains (DEDs)
and a caspase-like domain. FLIP interacts with adapter
protein FADD and caspase-8 and –10, and potently inhibits
apoptosis induced by all known death receptors CD95, DR3,
TRAIL-R and TNFR1. Four splice variants of c-FLIPs have
been identified and termed FLIPα, β, γ, and δ, respectively 8 .
SOURCE:
Rabbit anti-FLIP (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 191 to 209 at C-
terminus of human FLIPδ/FLIP s form 2 .
APPLICATION:
This antibody can be used for detection of FLIP by Western
blot at 1:1000 dilution. Jurkat cell lysate can be used as
positive control and 35 kDa and 25 kDa bands can be
detected. This antibody recognizes human and murine FLIPγ
and FLIPδ but not FLIPα and FLIPβ. For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of
FLIPγ/δ in total cell
lysates from HeLa (H),
Jurkat (J), THP-1 (T),
A431 (A), K562 (K) and
NIH3T3 (N) cells with
anti-FLIPγ/δ (CT) at
1:1000 dilution.
REFERENCES:
1. Thome M, Schneider P, Hofmann K, Fickenscher H, Meinl E, Neipel F,
Mattmann C, Burns K, Bodmer JL, Schroter M, Scaffidi C, Krammer PH,
Peter ME, Tschopp J. Viral FLICE-inhibitory proteins (FLIPs) prevent
apoptosis induced by death receptors . Nature 1997;386:517-521
2. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V,
Bodmer JL, Schroter M, Burns K, Mattmann C, Rimoldi D, French LE,
Tschopp J. Inhibition of death receptor signals by cellular FLIP. Nature
1997;388:190-195
3. Shu HB, Halpin DR, Goeddel DV. Casper is a FADD- and caspase-related
inducer of apoptosis. Immunity 1997;6:751-763
4. Hu S, Vincenz C, Ni J, Gentz R, Dixit VM. I-FLICE, a novel inhibitor of
tumor necrosis factor receptor-1- and CD-95-induced apoptosis . J Biol Chem
1997;272:17255-17257
5. Srinivasula SM, Ahmad M, Ottilie S, Bullrich F, Banks S, Wang Y,
Fernandes -Alnemri T, Croce CM, Litwack G, Tomaselli KJ, Armstrong RC,
Alnemri ES. FLAME-1, a novel FADD-like anti-apoptotic molecule that
regulates Fas/TNFR1-induced apoptosis. J Biol Chem 1997;272:18542-
18545
6. Goltsev YV, Kovalenko AV, Arnold E, Varfolomeev EE, Brodianskii VM,
Wallach D. CASH, a novel caspase homologue with death effector domains.
J Biol Chem 1997;272:19641-19644
7. Inohara N, Koseki T, Hu Y, Chen S, Nunez G. CLARP, a death effector
domain-containing protein interacts with caspase-8 and regulates apoptosis.
Proc Natl Acad Sci USA 1997;94:10717-10722
8. Tschopp J, Irmler M, Thome M. Inhibition of fas death signals by FLIPs.
Curr Opin Immunol 1998;10:552-8 (RD 1299)

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Anti-DNase II (CT)
CATALOG No.: 2059
BACKGROUND:
Apoptosis is characterized by several morphological nuclear
changes including chromatin condensation and nuclear
fragmentation. These changes are triggered by the activation
of members of caspase family, caspase activated DNase,
and several novel proteins including AIF and Acinus (1).
DNase II causes both chromatin condensation and DNA
fragmentation (1). The genes encoding human (2-4), porcine
(4), and murine (5) DNase II have been cloned. The DNase
II gene encodes a 40 kDa proenzyme. The mature enzyme
consists of two non-identical subunits, the 32 kDa (α) and 12
kDa (β) chains, generated by proteolytic processing.
Overexpression of DNase II induces chromatin condensation
(3). DNase II is ubiquitously expressed in human tissues.
SOURCE:
Rabbit anti-DNase II (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 347 to 360
of human DNase II precursor (2-4).
APPLICATION:
This polyclonal antibody can be used for detection of DNase
II expression by Western blot at 1:500 to 1:1000 dilution.
Human spleen tissue lysate or THP-1 cell lysate can be used
as positive control and an approximate 40 kDa band can be
detected, which represents the pro-enzyme of DNase II. For
research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
DNase II in human spleen
tissue lysate in the absence
(lane 1) or presence (lane
2) of blocking peptide with
anti-DNase II (CT) at 1:500
dilution.
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death. Nature
1999;401:127-8
2. Yasuda T, Takeshita H, Iida R, Nakajima T, Hosomi O,
Nakashima Y, Kishi K. Molecular cloning of the cDNA encoding
human deoxyribonuclease II. J Biol Chem 1998;273:2610-6
3. Krieser RJ, Eastman A. The cloning and expression of human
deoxyribonuclease II. A possible role in apoptosis. J Biol Chem
1998;273:30909-14
4. Shiokawa D, Tanuma S. Cloning of cDNAs encoding porcine
and human DNase II. Biochem Biophys Res Commun
1998;247:864-9
5. Baker KP, Baron WF, Henzel WJ, Spencer SA. Molecular
cloning and characterization of human and murine DNase II. Gene
1998;215:281-9
(RD0400)

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Anti-Bim (IN) BOD
CATALOG No.: 2065
BACKGROUND:
Members in the Bcl-2 family are critical regulators of
apoptosis by either inhibiting or promoting cell death. Bcl-2
homology 3 (BH3) domain is a potent death domain. BH3
domain containing pro-apoptotic proteins, including Bad,
Bax, Bid, Bik, and Hrk, form a growing subclass of the Bcl-2
family. A novel BH3 domain containing protein was recently
identified and designated Bim or BOD in human, mouse and
rat (1,2). Bim/BOD interacts with diverse members in the
pro-survival Bcl-2 sub-family including Bcl-2, Bcl-x L and Bclw.
Bim/BOD induces apoptosis. The messenger RNA of Bim
is ubiquitously expressed in multiple tissues and cell lines
(1,2).
SOURCE:
Rabbit anti-Bim (IN) polyclonal antibody was raised against a
peptide corresponding to amino acids 22 to 40 of human
origin (1). The sequence is identical to that of mouse and
differs from that of rat by one amino acid.
APPLICATION:
This polyclonal antibody can be used for detection of Bim by
Western blot at 1:1000 dilution. Human K562 cell lysate can
be used as positive control and a 23 kDa band can be
detected. This antibody is human, mouse, and rat reactive.
This antibody is for research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of Bim in
K562 (K) and A549 (A) whole cell
lysates with anti-Bim (IN) at
1:1000 dilution.
REFERENCES:
1. O'Connor,L., Strasser,A., O'Reilly,L.A., Hausmann,G.,
Adams,J.M., Cory,S. and Huang,D.C. Bim: a novel member of the
Bcl-2 family that promotes apoptosis. EMBO J. 1998;17:384-395
2. Hsu, S.Y., Lin, P., and Hsueh, A.J. BOD (Bcl-2-related ovarian
death gene) is an ovarian BH3 domain-containing proapoptotic Bcl-
2 protein capable of dimerization with diverse antiapoptotic Bcl-2
members. Mol Endocrinol 1998;12:1432-40
(RD1299)

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Anti-ZIP kinase (IN)
CATALOG No.: 2067
BACKGROUND:
Apoptosis is mediated by death domain containing adapter
molecules and a caspase family of proteases. Certain
serine/threonine protein kinases, such as ASK-1 and RIP,
are mediators of apoptosis. A novel serine/threonine kinase
that mediates apoptosis was recently identified and
designated ZIP kinase (1). ZIP kinase contains an N-terminal
kinase domain and a C-terminal leucine zipper structure and
binds to ATF4 that is a member of ATF/CREB family. ZIP
kinase has high sequence homology to DAP kinase (deathassociated
protein kinase), which is a mediator of apoptosis
induced by gamma interferon. Overexpression of ZIP kinase
induces apoptosis. ZIP and DAP kinases represent a novel
kinase family, which mediates apoptosis through their
catalytic activities. The messenger RNA was ubiquitously
expressed in various tissues (1).
STORAGE:
Supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of ZIP
kinase in HeLa (H) and Jurkat
(J) whole cell lysates with
anti-ZIP kinase (IN) at 1:500
dilution.
REFERENCES:
1. Kawai T, Matsumoto M, Takeda K, Sanjo H, Akira S. ZIP kinase,
a novel serine/threonine kinase which mediates apoptosis. Mol Cell
Biol 1998;18:1642-51
(RD1299)
SOURCE:
Rabbit anti-ZIP kinase (IN) polyclonal antibody was raised
against a peptide corresponding to amino acids 279 to 298
of human origin (1).
APPLICATION:
This polyclonal antibody can be used for detection of ZIP
kinase by Western blot at 1:1000 dilution. Jurkat or HeLa
whole cell lysate can be used as positive control and a 52
kDa band should be detected. It has no cross response to
DAP kinase. It is human, mouse, and rat reactive. For
research use only.

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Anti-Caspase-9 (I16) ICE-LAP6, Mch6, Apaf-3
CATALOG No.: 2071
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
A novel member in the caspase family was recently
identified and designated ICE-LAP6, Mch6, and Apaf-3 (1-3).
Caspase-9 and Apaf-1 bind to each other, which leads to
caspase-9 activation (3). Caspase-9 is also activated by
granzyme B and CPP32 (1,2). Activated caspase-9 cleaves
and activates caspase-3 that is one of the key proteases,
being responsible for the proteolytic cleavage of many key
proteins in apoptosis (3). Caspase-9 play a central role in
cell death induced by a wide variety of apoptosis activators
including TNFα, TRAIL, anti-CD-95, FADD, and TRADD (4).
Caspase-9 is expressed in a variety of human tissues (1,2).
SOURCE:
Rabbit anti-caspase-9 (I16) polyclonal antibody was raised
against a peptide corresponding to amino acids 41 to 56 of
human caspase-9 (1-3).
APPLICATION:
This polyclonal antibody can be used for detection of
caspase-9 by Western blot at 1:1000 to 1:2000 dilution.
Whole cell lysate from HeLa cells can be used as positive
control and a 46 kDa band should be detected. It has no
cross response to other members in caspase family. It is
human, mouse, and rat reactive. This antibody is for
research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
caspase-9 in HeLa whole
cell lysate with anticaspase-9
(I16) at 1:1000
dilution.
REFERENCES:
1. Duan H, Orth K, Chinnaiyan AM, Poirier GG, Froelich CJ, He
WW, Dixit VM. ICE-LAP6, a novel member of the ICE/Ced-3 gene
family, is activated by the cytotoxic T cell protease granzyme B. J
Biol Chem 1996;271:16720-4
2. Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, Robertson N,
Armstrong RC, Wang L, Trapani JA, Tomaselli KJ, Litwack G,
Alnemri ES. The Ced-3/interleukin 1beta converting enzyme-like
homolog Mch6 and the lamin-cleaving enzyme Mch2alpha are
substrates for the apoptotic mediator CPP32. J Biol Chem
1996;271:27099-106
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M,
Alnemri ES, Wang X. Cytochrome c and dATP-dependent
formation of Apaf-1/caspase-9 complex initiates an apoptotic
protease cascade. Cell 1997;91:479-89
4. Pan G, O'Rourke K, Dixit VM. Caspase-9, Bcl-XL, and Apaf-1
form a ternary complex. J Biol Chem 1998;273:5841-5
(RD1299)

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Anti-Caspase-9 (I20) ICE-LAP6, Mch6, Apaf-3
CATALOG No.: 2073
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
A novel member in the caspase family was recently
identified and designated ICE-LAP6, Mch6, and Apaf-3 (1-3).
Caspase-9 and Apaf-1 bind to each other, which leads to
caspase-9 activation (3). Caspase-9 is also activated by
granzyme B and CPP32 (1,2). Activated caspase-9 cleaves
and activates caspase-3 that is one of the key proteases,
being responsible for the proteolytic cleavage of many key
proteins in apoptosis (3). Caspase-9 play a central role in
cell death induced by a wide variety of apoptosis activators
including TNFα, TRAIL, anti-CD-95, FADD, and TRADD (4).
Caspase-9 is expressed in a variety of human tissues (1,2).
SOURCE:
Rabbit anti-caspase-9 (I20) polyclonal antibody was raised
against a peptide corresponding to amino acids 299 to 318
of human caspase-9 (1-3).
APPLICATION:
This polyclonal antibody can be used for detection of
caspase-9 by Western blot at 1:1000 to 1:2000 dilution.
Whole cell lysate from HeLa cells can be used as positive
control and a 46 kDa band should be detected. It has no
cross response to other members in caspase family. This
antibody is for research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
caspase-9 in HeLa whole cell
lysate with anti-caspase-9
(I20) at 1:1000 dilution.
REFERENCES:
1. Duan H, Orth K, Chinnaiyan AM, Poirier GG, Froelich CJ, He
WW, Dixit VM. ICE-LAP6, a novel member of the ICE/Ced-3 gene
family, is activated by the cytotoxic T cell protease granzyme B. J
Biol Chem 1996;271:16720-4
2. Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, Robertson N,
Armstrong RC, Wang L, Trapani JA, Tomaselli KJ, Litwack G,
Alnemri ES. The Ced-3/interleukin 1beta converting enzyme-like
homolog Mch6 and the lamin-cleaving enzyme Mch2alpha are
substrates for the apoptotic mediator CPP32. J Biol Chem
1996;271:27099-106
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M,
Alnemri ES, Wang X. Cytochrome c and dATP-dependent
formation of Apaf-1/caspase-9 complex initiates an apoptotic
protease cascade. Cell 1997;91:479-89
4. Pan G, O'Rourke K, Dixit VM. Caspase-9, Bcl-XL, and Apaf-1
form a ternary complex. J Biol Chem 1998;273:5841-5.
(RD1299)

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Anti-RICK (NT) RIP2, CARDIAK
CATALOG No.: 2075
BACKGROUND:
Apoptosis is mediated by death domain (DD) and/or caspase
recruitment domain (CARD) containing molecules and a
caspase family of proteases. DD-containing serine/threonine
kinase RIP regulates Fas-induced apoptosis. A novel CARDcontaining
serine/threonine kinase was recently identified
and designated RICK/RIP2/CARDIAK for RIP-like interacting
CLARP kinase, receptor interacting protein-2, and CARDcontaining
ICE associated kinase, respectively, (1-3). RICK
contains an N-terminal kinase catalytic domain and a C-
terminal CARD domain. Overexpression of RICK induced
apoptosis and activation of NF-κB and JNK. RICK interacts
with members of the TRAF family, CLARP and caspase-1.
Thus, RICK represents a novel kinase that regulates TNF
and Fas induced-apoptosis and that is involved in the
generation of proinflammatory cytokine IL-1β. The
messenger RNA of RICK is expressed in multiple human
tissues (1).
SOURCE:
Rabbit anti-RICK (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 11 to 30 of
human origin (1).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
RICK in A431 (A) and K562
(K) whole cell lysate with
anti-RICK (NT) at 1:1000
dilution.
REFERENCES:
1. Inohara N, del Peso L, Koseki T, Chen S, Nunez G. RICK, a
novel protein kinase containing a caspase recruitment domain,
interacts with CLARP and regulates CD95-mediated apoptosis. J
Biol Chem 1998;273:12296-300
2. McCarthy JV, Ni J, Dixit VM. RIP2 is a novel NF-kappaBactivating
and cell death-inducing kinase. J Biol Chem
1998;273:16968-75
3. Thome M, Hofmann K, Burns K, Martinon F, Bodmer JL,
Mattmann C, Tschopp J. Identification of CARDIAK, a RIP-like
kinase that associates with caspase-1. Curr Biol 1998;8:885-8
(RD1299)
APPLICATION:
This polyclonal antibody can be used for detection of RICK
by Western blot at 1:1000 dilution. A431 or K562 whole cell
lysate can be used as positive control and an approximately
60 kDa band can be detected. It is human, mouse, and rat
reactive. For research use only.

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Anti-ARC (CT)
CATALOG No.: 2081
BACKGROUND:
Apoptosis is regulated by death domain (DD) and/or
caspase recruitment domain (CARD) containing molecules
and a caspase family of proteases. CARD domain containing
cell death regulators include RAIDD, Apaf-1, caspase-9, and
caspase-2. A novel CARD domain containing protein was
recently identified and designated ARC for apoptosis
repressor with CARD (1). ARC interacts with caspase-2 and
–8 and inhibits enzymatic activity of caspase-8. ARC
suppresses apoptosis induced by cell death adapters FADD
and TRADD and by cell death receptors Fas, TNFR-1 and
DR3. The messenger RNA of ARC is primarily expressed in
skeletal muscle and cardiac tissue (1).
SOURCE:
Rabbit anti-ARC (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 191 to 208 of human
origin (1).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
ARC in HeLa (H), KB (K),
and A549 (A) whole cell
lysates with anti-ARC (CT)
at 1:1000 dilution.
REFERENCES:
1. Koseki T, Inohara N, Chen S, Nunez G. ARC, an inhibitor of
apoptosis expressed in skeletal muscle and heart that interacts
selectively with caspases. Proc Natl Acad Sci U S A 1998;95:5156-
60 (RD1299)
APPLICATION:
This polyclonal antibody can be used for detection of ARC
by Western blot at 1:1000 dilution. Whole cell lysate from
HeLa cells can be used as positive control and an
approximately 25 kDa band can be detected. This antibody
is for research use only.

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Anti-CIDE-A (CT)
CATALOG No.: 2085
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors. Cell death signals are
transduced by DD-, DED-, or CARD-containing molecules
and members of the caspase family of proteases. These
death signals finally cause the degradation of chromosomal
DNA by activated DNase DFF40/CAD, which is chaperoned
and inhibited by DFF45/ICAD (1-4). DFF45 related proteins
CIDE-A and CIDE-B (for cell death-inducing DFF-like
effector A and B) were recently identified (5). CIDE contains
a new type of domain termed CIDE-N, which has high
homology with the regulatory domains of DFF45/ICAD and
DFF40/CAD (5,6). Expression of CIDE-A induces DNA
fragmentation and activates apoptosis, which is inhibited by
DFF45. CIDE-A is expressed in many tissues.
SOURCE:
Rabbit anti-CIDE-A (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 200 to 217
of human CIDE-A (5).
APPLICATION:
This polyclonal antibody can be used for detection of CIDE-A
by Western blot at 1:1000 to 1:2000 dilution. Human brain
tissue lysate can be used as positive control and an
approximately 23 kDa band can be detected. It has no cross
activity to CIDE-B. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2085P). Human brain tissue lysate,
200 µl/100 µl, is available for positive control (Catalog No.
1303).
Western blot analysis of
CIDE-A in human brain tissue
lysate in the absence (A) or
presence (B) of peptide
(2085P) with anti-CIDE-A
(CT) at 1:2000 dilution.
REFERENCES:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184 2. Enari M,
Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A
caspase-activated DNase that degrades DNA during apoptosis,
and its inhibitor ICAD. Nature 1998;391:43-50
3. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
4. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
5. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel
family of cell death activators with homology to the 45 kDa subunit
of the DNA fragmentation factor. EMBO J 1998;17:2526-33
6. Lugovskoy AA, Zhou P, Chou JJ, McCarty JS, Li P, Wagner G.
Solution structure of the CIDE-N domain of CIDE -B and a model
for CIDE-N/CIDE -N interactions in the DNA fragmentation pathway
of apoptosis. Cell 1999;99(7):747-55
(WD0300)

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Anti-CIDE-A (CT)
CATALOG No.: 2089
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. DFF45/ICAD has
been identified as inhibitor of caspase activated DNase
DFF40/CAD. DFF45 related proteins CIDE-A and CIDE-B
(for cell death-inducing DFF-like effector A and B) were
recently identified (1). CIDE contains a new type of domain
termed CIDE-N, which has high homology with the
regulatory domains of DFF45/ICAD and DFF40/CAD (1,2).
Expression of CIDE-A induces DNA fragmentation and
activates apoptosis, which is inhibited by DFF45. CIDE-A is
a DFF45-inhibitable effector that promotes cell death and
DNA fragmentation. CIDE-A is expressed in many tissues.
STORAGE:
Supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of
CIDE-A in murine heart
tissue lysate with anti-CIDE-A
(CT) at 1:500 dilution.
RELATED PRODUCTS:
Blocking peptide, 100 µg / 500 µl, is available for
competition studies (Catalog No. 2089P).
Murine heart tissue lysate, 500 µg / 200 µl, is available for
positive control (Catalog No. 1253).
SOURCE:
Rabbit anti-CIDE-A (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 200 to 214
of mouse CIDE-A (1).
REFERENCES:
1. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel
family of cell death activators with homology to the 45 kDa subunit
of the DNA fragmentation factor. EMBO J 1998;17:2526-33
APPLICATION:
This polyclonal antibody can be used for detection of CIDE-A
by Western blot at 1:500 to 1:1000 dilution. Tissue lysate of
murine heart can be used as positive control and an
approximately 25 kDa band can be detected. It has no cross
activity to CIDE-B. This antibody is for research use only.
2. Inohara N, Koseki T, Chen S, Benedict MA, Nunez G.
Identification of regulatory and catalytic domains in the apoptosis
nuclease DFF40/CAD. J Biol Chem 1999 ;274:270-4
(RD1299)

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Anti-CIDE-B (CT)
CATALOG No.: 2091
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. DFF45/ICAD has
been identified as inhibitor of caspase activated DNase
DFF40/CAD. DFF45 related proteins CIDE-A and CIDE-B
(for cell death-inducing DFF-like effector A and B) were
recently identified (1). CIDE contains a new type of domain
termed CIDE-N, which has high homology with the
regulatory domains of DFF45/ICAD and DFF40/CAD (1,2).
Expression of CIDE-B induces apoptosis, which is inhibited
by DFF45. CIDE-B is a DFF45-inhibitable effector that
promotes cell death and DNA fragmentation. CIDE-B is
expressed mainly in liver and at lower levels in spleen,
kidney, peripheral blood lymphocytes, and bone marrow (1).
SOURCE:
Rabbit anti-CIDE-B (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 204 to 219
of murine CIDE-B (1).
APPLICATION:
This polyclonal antibody can be used for detection of CIDE-B
by Western blot at 1:500 to 1:1000 dilution. Tissue lysate of
murine liver can be used as positive control and an
approximately 25 kDa band can be detected. It has no cross
activity to CIDE-A. This antibody is for research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
CIDE-B in murine liver tissue
lysate with anti-CIDE-B (CT)
at 1:500 dilution.
RELATED PRODUCTS:
Blocking peptide, 100 µg / 500 µl, is available for
competition studies (Catalog No. 2091P).
Murine liver tissue lysate, 500 µg / 200 µl, is available for
positive control (Catalog No. 1254).
REFERENCES:
1. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel
family of cell death activators with homology to the 45 kDa subunit
of the DNA fragmentation factor. EMBO J 1998;17:2526-33
2. Inohara N, Koseki T, Chen S, Benedict MA, Nunez G.
Identification of regulatory and catalytic domains in the apoptosis
nuclease DFF40/CAD. J Biol Chem 1999 ;274:270-4
(RD1299)

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Anti-CX 3 CR1 (NT) V28, CMKBRL1
CATALOG NO.: 2093
BACKGROUND:
CX 3 CR1 is one of the chemokine receptors that are required
as coreceptors for HIV infection. The genes encoding
human, murine, and rat CX 3 CR1 were cloned and
designated V28 and CMKBRL1, CX 3 CR1, and RBS11,
respectively, (1-4). The encoded seven transmembrane
protein was recently identified as the receptor for a novel
transmembrane molecule, fractalkine, and renamed CX 3 CR1
(5). Recently, CX 3 CR1 was found to serve as a coreceptor
for HIV-1 and HIV-2 envelope fusion and virus infection,
which can be inhibited by fractokine (6). CX 3 CR1 mediates
leukocyte migration and adhesion (5). CX 3 CR1 is expressed
in a variety of human tissues and cell lines (2).
SOURCE:
Rabbit anti-CX 3 CR1 polyclonal antibody was raised against
a peptide corresponding to amino acids 2 to 21 of human
CX 3 CR1 (1,2). The sequence differs from those of mouse
and rat CX 3 CR1 by four amino acids (3,4)
APPLICATION:
This polyclonal antibody can be used for detection of
CX 3 CR1 by Western blot at 1:500 to 1:2000 dilution. Human
spleen tissue lysate can be used as positive control and an
approximately 50 kDa band can be detected. It is human,
mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
CX 3 CR1 in human spleen
lysate with anti-CX 3 CR1 in the
absence (lane 1) or presence
of blocking peptide (lane 2).
REFERENCES:
1. Raport CJ, Schweickart VL, Eddy RL JR, Shows TB, Gray PW. The
orphan G-protein-coupled receptor-encoding gene V28 is closely related to
genes for chemokine receptors and is expressed in lymphoid and neural
tissues. Gene 1995;163:295-9
2. Combadiere C, Ahuja SK, Murphy PM. Cloning, chromosomal localization,
and RNA expression of a human beta chemokine receptor-like gene. DNA
Cell Biol 1995;14:673-80
3. Combadiere C, Gao J, Tiffany HL, Murphy PM. Gene cloning, RNA
distribution, and functional expression of mCX3CR1, a mouse chemotactic
receptor for the CX3C chemokine fractalkine. Biochem Biophys Res
Commun 1998;253:728-32
4. Harrison JK, Barber CM, Lynch KR. cDNA cloning of a G-protein-coupled
receptor expressed in rat spinal cord and brain related to chemokine
receptors. Neurosci Lett 1994;169:85-9
5. Imai T, Hieshima K, Haskell C, Baba M, Nagira M, Nishimura M, Kakizaki
M, Takagi S, Nomiyama H, Schall TJ, Yoshie O. Identification and molecular
characterization of fractalkine receptor CX3CR1, which mediates both
leukocyte migration and adhesion. Cell 1997;91:521-30
6. Combadiere C, Salzwedel K, Smith ED, Tiffany HL, Berger EA, Murphy
PM. Identification of CX3CR1. A chemotactic receptor for the human CX3C
chemokine fractalkine and a fusion coreceptor for HIV-1. J Biol Chem
1998;273:23799-804 (RD1299)

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Anti-CCR8 TER1, CKR-L1, ChemR1
CATALOG NO.: 2097
BACKGROUND:
CCR8 is one of the chemokine receptors that are required as
coreceptors for HIV infection. The genes encoding human
and murine CCR8 were cloned and designated TER1, CKR-
L1, and ChemR1 (1-4). The encoded seven transmembrane
protein was identified as the receptor for human CC
chemokine I-309 and renamed CCR8. Recently, CCR8 was
found to serve as a coreceptor for diverse T-cell tropic, dualtropic
and macrophage-tropic HIV-1 strains (5). CCR8
mediates CC chemokine I-309 induced monocyte
chemoattraction and HIV-1 envelope fusion and virus
infection, which can be prevented by the CCR8 ligand I-309.
CCR8 is expressed in spleen, thymus and T lymphoblastic
cell lines.
SOURCE:
Rabbit anti-CCR8 polyclonal antibody was raised against a
peptide corresponding to amino acids 183 to 201 of human
CCR8, which locate in the second extracellular loop (1-3).
APPLICATION:
This polyclonal antibody can be used for detection of CCR8
by Western blot at 1:500 to 1:1000 dilution. Human spleen
tissue lysate can be used as positive control and an
approximately 50 kDa band can be detected. For research
use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of
CCR8 in human spleen lysate
with anti-CCR8 at 1:500
dilution.
REFERENCES:
1. Napolitano M, Zingoni A, Bernardini G, Spinetti G, Nista A,
Storlazzi CT, Rocchi M, Santoni A. Molecular cloning of TER1, a
chemokine receptor-like gene expressed by lymphoid tissues. J
Immunol 1996;157:2759-63
2. Zaballos A, Varona R, Gutierrez J, Lind P, Marquez G.
Molecular cloning and RNA expression of two new human
chemokine receptor-like genes. Biochem Biophys Res Commun
1996;227:846-53
3. Samson M, Stordeur P, Labbe O, Soularue P, Vassart G,
Parmentier M. Molecular cloning and chromosomal mapping of a
novel human gene, ChemR1, expressed in T lymphocytes and
polymorphonuclear cells and encoding a putative chemokine
receptor. Eur J Immunol 1996;26:3021-8
4. Goya I, Gutierrez J, Varona R, Kremer L, Zaballos A, Marquez
G. Identification of CCR8 as the specific receptor for the human
beta-chemokine I-309: cloning and molecular characterization of
murine CCR8 as the receptor for TCA-3. J Immunol
1998;160:1975-81
5. Horuk R, Hesselgesser J, Zhou Y, Faulds D, Halks-Miller M,
Harvey S, Taub D, Samson M, Parmentier M, Rucker J, Doranz
BJ, Doms RW. The CC chemokine I-309 inhibits CCR8-dependent
infection by diverse HIV-1 strains. J Biol Chem 1998;273:386-91
(WD1299)

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Anti-GPR15 (NT) BOB
CATALOG NO.: 2101
BACKGROUND:
Human immunodeficiency virus (HIV) and related viruses
require coreceptors to infect target cells. Some G proteincoupled
receptors including CCR5, CXCR4, CCR3, CCR2b
and CCR8 in the chemokine receptor family, and four new
human molecules GPR15, STRL33, GPR1 and V28 were
recently identified as HIV coreceptors. The genes encoding
human and monkey GPR15/BOB (for G protein-coupled
receptor 15 and brother of Bonzo, respectively,) were
recently cloned (1,2). This novel G protein-coupled receptor
serves as corecptor for simian immunodeficiency virus (SIV),
and for strains of HIV-2 and M-tropic HIV-1 (2,3). The ligand
for GPR15 has not been identified yet.
SOURCE:
Rabbit anti-GPR15/BOB polyclonal antibody was raised
against a peptide corresponding to amino acids 13 to 28 of
human GPR15 (1). The sequence differs from those of
African green monkey and pig-tailed macaque BOB by one
amino acid (2)
APPLICATION:
This polyclonal antibody can be used for detection of
GPR15/BOB by Western blot at 1:500 to 1:2000 dilution.
Jurkat or A549 cell lysate can be used as positive control
and an approximately 50 kDa band can be detected. It is
human, mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of GPR15 in
human heart lysate with anti-
GPR15 (NT) in the absence (lane
1) or presence of specific peptide
(lane 2) or non-related peptide
(lane 3).
REFERENCES:
1. Heiber M, Marchese A, Nguyen T, Heng HH, George SR,
O'Dowd BF. A novel human gene encoding a G-proteincoupled
receptor (GPR15) is located on chromosome 3. Genomics
1996;32:462-5
2. Deng HK, Unutmaz D, KewalRamani VN, Littman DR.
Expression cloning of new receptors used by simian and human
immunodeficiency viruses. Nature 199;388:296-300
3. Farzan M, Choe H, Martin K, Marcon L, Hofmann W, Karlsson
G, Sun Y, Barrett P, Marchand N, Sullivan N, Gerard N, Gerard C,
Sodroski J. Two orphan seven-transmembrane segment receptors
which are expressed in CD4-positive cells support simian
immunodeficiency virus infection. J Exp Med 1997;186:405-11
(RD1299)

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Anti-DFF40/CAD (I18)
CATALOG No.: 2107
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A mouse DNase
that causes DNA fragmentation was identified recently and
designated CAD (for caspase activated deoxyribonuclease)
(1,2). The human homologue of mouse CAD was more
recently identified by three groups independently and termed
CPAN, DFF40, and human CAD, respectively, (3-5).
DFF45/ICAD is the inhibitory protein of DFF40/CAD (1,2,6)
and forms complex with DFF40/CAD. Upon cleavage of
DFF45/ICAD by activated caspase, DFF40/CAD is released
and activated and eventually causes the degradation of DNA
in the nuclei. Activation of DFF40/CAD, which causes DNA
degradation, is the hallmark of apoptotic cell death.
SOURCE:
Rabbit anti-CAD (I18) polyclonal antibody was raised against
a peptide corresponding to amino acids 147 to 164 of murine
CAD (1). The sequence differs from human DFF40 by two
amino acids (3,4)
APPLICATION:
This polyclonal antibody can be used for detection of
DFF40/CAD by Western blot at 1:500 to 1:1000 dilution.
K562 or Jurkat whole cell lysate can be used as positive
control and a 40 kDa band can be detected. It is human,
mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100 µg
in 200 µl of PBS containing 0.02% sodium azide. Store at
4°C, stable for one year.
Western blot analysis of
DFF40/CAD in HeLa (H),
K562 (K), Jurkat (J), and
Raji (R) whole cell lysate
with anti-DFF40/CAD (I18)
at 1:500 dilution.
REFERENCES:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
2. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
3. Halenbeck R, MacDonald H, Roulston A, Chen TT, Conroy L,
Williams LT. CPAN, a human nuclease regulated by the caspasesensitive
inhibitor DFF45. Curr Biol 1998;8:537-40
4. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
5. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H,
Nagata S. Molecular cloning + characterization of human caspaseactivated
DNase. Proc Natl Acad Sci USA 1998;95:9123-8
6. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
(RD1299)

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Anti-IKKα/IKK-1 (C2)
CATALOG No.: 2115
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα and
bacteria product LPS. NF-κB is associated with IκB proteins
in the cell cytoplasm, which inhibit NF-κB activity. The longsought
IκB kinase (IKK), which phosphorylates IκB, and
mediates IκB degradation and NF-κB activation, was
recently identified by several laboratories (1-5). IKK is a
serine protein kinase, and the IKK complex contains alpha
and beta subunits (IKKα and IKKβ). IKKα and IKKβ interact
with each other and both are essential for the NF-κB
activation. IKKα specifically phosphorylates IκB-α. IKKα is
expressed in a variety of human tissues.
SOURCE:
Rabbit anti-IKKα (C2) polyclonal antibody was raised against
a peptide corresponding to amino acids 699 to 715 of human
IKKα (1,2), which differs from corresponding murine
sequence by one amino acid.
APPLICATION:
This polyclonal antibody can be used for detection of IKKα
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from HeLa cells can be used as positive control and an 85
kDa band should be detected. It has no cross response to
IKKβ or IKKγ. For research use only.
Western blot analysis of
IKKα in HeLa whole cell
lysate with anti-IKKα (C2)
at 1:500 dilution.
REFERENCES:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A
cytokine-responsive IkappaB kinase that activates the transcription
factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M.
Identification and characterization of an IkappaB kinase. Cell
1997;90:373-83
3. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The
IkappaB kinase complex (IKK) contains two kinase subunits,
IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and
NF-kappaB activation. Cell 1997;91:243-52
4. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DY. IkappaB
kinase-beta: NF-kappaB activation and complex formation with
IkappaB kinase-alpha and NIK. Science 1997;278:866-9
5. Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J,
Young DB, Barbosa M, Mann M, Manning A, Rao A. IKK-1 and
IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB
activation. Science 1997;278:860-6 (RD1299)
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.

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Anti-IKKα (C3)
CATALOG No.: 2117
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα, and
bacteria product LPS. NF-κB is associated with IκB proteins
in the cell cytoplasm, which inhibit NF-κB activity. The longsought
IκB kinase (IKK), which phosphorylates IκB, and
mediates IκB degradation and NF-κB activation, was
recently identified by several laboratories (1-5). IKK is a
serine protein kinase, and the IKK complex contains alpha
and beta subunits (IKKα and IKKβ). IKKα and IKKβ interact
with each other and both are essential for the NF-κB
activation. IKKα specifically phosphorylates IκB-α. IKKα is
expressed in a variety of human tissues.
SOURCE:
Rabbit anti-IKKα (C3) polyclonal antibody was raised against
a peptide corresponding to amino acids 658 to 674 of human
IKKα (1,2), which differs from corresponding murine
sequence by one amino acid.
APPLICATION:
This polyclonal antibody can be used for detection of IKKα
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from Jurkat cells can be used as positive control and an 85
kDa band should be detected. It has no cross response to
IKKβ or IKKγ. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
IKKα in Jurkat whole cell
lysate with anti-IKKα (C3)
at 1:500 dilution.
REFERENCES:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A
cytokine-responsive IkappaB kinase that activates the transcription
factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M.
Identification and characterization of an IkappaB kinase. Cell
1997;90:373-83
3. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The
IkappaB kinase complex (IKK) contains two kinase subunits,
IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and
NF-kappaB activation. Cell 1997;91:243-52
4. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DY. IkappaB
kinase-beta: NF-kappaB activation and complex formation with
IkappaB kinase-alpha and NIK. Science 1997;278:866-9
5. Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J,
Young DB, Barbosa M, Mann M, Manning A, Rao A. IKK-1 and
IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB
activation. Science 1997;278:860-6
(RD1299)

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Suite 207
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IKKβ (C3)
CATALOG No.: 2121
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli including IL-1, TNFα, and
bacteria product LPS. NF-κB is associated with IκB proteins
in the cell cytoplasm, which inhibit NF-κB activity. The longsought
IκB kinase (IKK), which phosphorylates IκB, and
mediates IκB degradation and NF-κB activation, was
recently identified by several laboratories (1-5). IKK is a
serine protein kinase, and the IKK complex contains alpha
and beta subunits (IKKα and IKKβ). IKKα and IKKβ interact
with each other and both are essential for NF-κB activation.
IKKβ phosphorylates both IκB-α and IκB-β. IKKβ is
expressed in variety of human tissues.
SOURCE:
Rabbit anti-IKKβ (C3) polyclonal antibody was raised against
a peptide corresponding to amino acids 662 to 680 of human
IKKβ (3,4), which differs from corresponding murine
sequence by one amino acid (5).
APPLICATION:
This polyclonal antibody can be used for detection of IKKβ
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from Jurkat cells can be used as positive control and an 87
kDa band should be detected. It has no cross response to
IKKα or IKKγ. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of IKKβ
in Jurkat whole cell lysate with
anti-IKKβ (C3) at 1:500
dilution.
REFERENCES:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A
cytokine-responsive IkappaB kinase that activates the transcription
factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M.
Identification and characterization of an IkappaB kinase. Cell
1997;90:373-83
3. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The
IkappaB kinase complex (IKK) contains two kinase subunits,
IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and
NF-kappaB activation. Cell 1997;91:243-52
4. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DY. IkappaB
kinase-beta: NF-kappaB activation and complex formation with
IkappaB kinase-alpha and NIK. Science 1997;278:866-9
5. Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J,
Young DB, Barbosa M, Mann M, Manning A, Rao A. IKK-1 and
IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB
activation. Science 1997;278:860-6
6. Nakano H, Shindo M, Sakon S, Nishinaka S, Mihara M, Yagita
H, Okumura K. Differential regulation of IkappaB kinase alpha and
beta by two upstream kinases, NF-kappaB-inducing kinase and
mitogen-activated protein kinase/ERK kinase kinase-1. Proc Natl
Acad Sci U S A 1998;95:3537-42
(RD1299)

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Anti-IRAK2 (C2)
CATALOG No.: 2123
BACKGROUND:
The pro-inflammatory cytokine IL-1 induces cellular
response through two subunits of its receptor, IL-1 receptor I
(IL-1RI) and IL-1 receptor accessory protein (IL-1RAcP). IL-1
receptor-associated kinase (IRAK) mediates activation of
NF-κB, which is a pivotal transcription factor mediating
inflammatory and immune response. A novel member in the
IRAK/Pelle family was recently identified and designated
IRAK2 (1). Both IRAK and IRAK2 recruit to the subunits of
the IL-1R complex after IL-1 binding and lead to NF-κB
activation. IRAKs also associate with Toll like receptor (TLR)
and the dominant negative mutants of IRAKs inhibit LPSinduced
NF-κB activation (2,3). Members in IRAK/Pelle
family play a central role in IL-1R and TLR mediated
inflammatory response. IRAK2 is expressed in a variety of
human tissues.
SOURCE:
Rabbit anti-IRAK2 (C2) polyclonal antibody was raised
against a peptide corresponding to amino acid 546 to 564 of
human IRAK2 (1).
APPLICATION:
This polyclonal antibody can be used for detection of IRAK2
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from HeLa or K562 cells can be used as positive control and
a 65 kDa band should be detected. Anti-IRAK2 has no cross
response to IRAK. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
IRAK2 in HeLa (H) and K562
(K) whole cell lysate with anti-
IRAK2 (C2) at 1:500 dilution.
REFERENCES:
1. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member
IRAK-2 and MyD88 as proximal mediators of IL-1 signaling.
Science 1997;278:1612-5
2. Zhang FX, Kirschning CJ, Mancinelli R, Xu XP, Jin Y, Faure E,
Mantovani A, Rothe M, Muzio M, Arditi M. Bacterial
lipopolysaccharide activates nuclear factor-kappaB through
interleukin-1 signaling mediators in cultured human dermal
endothelial cells and mononuclear phagocytes. J Biol Chem
1999;274:7611-4
3. Yang RB, Mark MR, Gurney AL, Godowski PJ. Signaling events
induced by lipopolysaccharide-activated toll-like receptor 2. J
Immunol 1999;163:639-43
(RD1299)

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Anti-MyD88 (IN)
CATALOG No.: 2125
BACKGROUND:
The pro-inflammatory cytokine IL-1 induced cellular
response requires IL-1 receptor complex including IL-1RI
and IL-1RAcP. Recently, MyD88 was identified as an
adapter molecule in the IL-1 signaling pathway (1). MyD88
associates with and recruits IRAK to the IL-1 receptor
complex in response to IL-1 treatment and dominant
negative form of MyD88 attenuates IL-1R-mediated NF-κB
activation. MyD88 is also employed as a regulator molecule
by IL-18 receptor and human Toll receptor (2,3), which are
members in the Toll/IL-1R family of receptors. Targeted
disruption of the MyD88 gene results in lose of cellular
responses to IL-1 and IL-18, and MyD88-deficient mice lack
responses to bacterial product LPS that employs Toll-like
receptors 2 and 4 (TLR2 and TLR4) as the signaling
receptors. MyD88 is a general adapter protein for the
Toll/IL-1R family of receptors and plays an important role in
the inflammatory response induced by cytokines IL-1 and IL-
18 and endotoxin. MyD88 gene is expressed in many
tissues.
SOURCE:
Rabbit anti-MyD88 (IN) polyclonal antibody was raised
against a peptide corresponding to amino acids 233 to 248
of human MyD88 (5), which differ from those of mouse by
two amino acids.
APPLICATION:
This polyclonal antibody can be used for detection of MyD88
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from Jurkat cells can be used as positive control and an
approximately 35 kDa band can be detected. It is human and
mouse reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
MyD88 in Jurkat whole cell
lysate with anti-MyD88 (IN)
at 1:500 dilution.
REFERENCES:
1. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member
IRAK-2 and MyD88 as proximal mediators of IL-1 signaling.
Science 1997;278:1612-5
2. Adachi O, Kawai T, Takeda K, Matsumoto M, Tsutsui H,
Sakagami M, Nakanishi K, Akira S. Targeted disruption of the
MyD88 gene results in loss of IL-1- and IL-18-mediated function.
Immunity 1998;9:143-50
3. Medzhitov R, Preston-Hurlburt P, Kopp E, Stadlen A, Chen C,
Ghosh S, Janeway CA Jr. MyD88 is an adaptor protein in the
hToll/IL-1 receptor family signaling pathways. Mol Cell 1998;2:253-
8
4. Kawai T, Adachi O, Ogawa T, Takeda K, Akira S.
Unresponsiveness of MyD88-deficient mice to endotoxin. Immunity
1999;11:115-22
5. Bonnert TP, Garka KE, Parnet P, Sonoda G, Testa JR, Sims JE.
The cloning and characterization of human MyD88: amember of an
IL-1 receptor related family. FEBS Lett 1997;402:81-4
(RD1299)

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www.prosci-inc.com
Toll Free: 888-513-9525
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Anti-MyD88 (CT)
CATALOG No.: 2127
BACKGROUND:
The pro-inflammatory cytokine IL-1 induced cellular
response requires IL-1 receptor complex including IL-1RI
and IL-1RAcP. Recently, MyD88 was identified as an
adapter molecule in the IL-1 signaling pathway (1). MyD88
associates with and recruits IRAK to the IL-1 receptor
complex in response to IL-1 treatment and dominant
negative form of MyD88 attenuates IL-1R-mediated NF-κB
activation. MyD88 is also employed as a regulator molecule
by IL-18 receptor and human Toll receptor (2,3), which are
members in the Toll/IL-1R family of receptors. Targeted
disruption of the MyD88 gene results in lose of cellular
responses to IL-1 and IL-18, and MyD88-deficient mice lack
responses to bacterial product LPS that employs Toll-like
receptors 2 and 4 (TLR2 and TLR4) as the signaling
receptors. MyD88 is a general adapter protein for the
Toll/IL-1R family of receptors and plays an important role in
the inflammatory response induced by cytokines IL-1 and IL-
18 and endotoxin. MyD88 gene is expressed in many
tissues.
SOURCE:
Rabbit anti-MyD88 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 279 to 296
of human MyD88 (5), which are identical to those of mouse.
APPLICATION:
This polyclonal antibody can be used for detection of MyD88
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from Jurkat cells can be used as positive control and an
approximately 35 kDa band can be detected. It is human and
mouse reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
MyD88 in Jurkat whole cell
lysate with anti-MyD88 (CT)
at 1:500 dilution.
REFERENCES:
1. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member
IRAK-2 and MyD88 as proximal mediators of IL-1 signaling.
Science 1997;278:1612-5
2. Adachi O, Kawai T, Takeda K, Matsumoto M, Tsutsui H,
Sakagami M, Nakanishi K, Akira S. Targeted disruption of the
MyD88 gene results in loss of IL-1- and IL-18-mediated function.
Immunity 1998;9:143-50
3. Medzhitov R, Preston-Hurlburt P, Kopp E, Stadlen A, Chen C,
Ghosh S, Janeway CA Jr. MyD88 is an adaptor protein in the
hToll/IL-1 receptor family signaling pathways. Mol Cell 1998;2:253-
8
4. Kawai T, Adachi O, Ogawa T, Takeda K, Akira S.
Unresponsiveness of MyD88-deficient mice to endotoxin. Immunity
1999;11:115-22
5. Bonnert TP, Garka KE, Parnet P, Sonoda G, Testa JR, Sims JE.
The cloning and characterization of human MyD88: a member of
an IL-1 receptor related family. FEBS Lett 1997;402:81-4
(RD1299)

13100 Kirkham Way
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techsupport@prosci-inc.com
Anti-IL-1RAcP (C2)
CATALOG No.: 2129
BACKGROUND:
The pro-inflammatory cytokine IL-1 induced cellular
response requires two subunits of its receptor, IL-1 receptor I
(IL-1RI) and IL-1 receptor accessory protein (IL-1RAcP) (1).
IL-1RAcP forms a complex with IL-1RI in response to IL-1
treatment. The IL-1 receptor-associated kinase (IRAK),
which mediates activation of NF-κB inducing kinae (NIK) and
of NF-κB, recruits to the IL-1R complex through IL-1RAcP
(2). IL-1 activation of stress-activated protein kinase and of
acid sphingomyelinase also requires IL-1RAcP (3,4). Like
IL-1RI, IL-1RAcP subunit is essential for IL-1 mediated
cellular response. IL-1RAcP is expressed in many tissues.
SOURCE:
Rabbit anti-IL-1RAcP (C2) polyclonal antibody was raised
against a peptide corresponding to amino acids 525 to 540
of human IL-1RAcP, which is identical to those of mouse and
rat origins (1).
APPLICATION:
This polyclonal antibody can be used for detection of IL-
1RAcP by Western blot at 1:1000 to 1:2000 dilution. Whole
cell lysate from HeLa cells can be used as positive control
and an approximately 66 kDa band can be detected. It is
human, mouse, and rat reactive, and has no cross activity to
other members in the IL-1 receptor family. For research use
only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of IL-
1RAcP in HeLa whole cell
lysate with anti-IL-1RAcP (C2)
at 1:1000 dilution.
REFERENCES:
1. Greenfeder SA, Nunes P, Kwee L, Labow M, Chizzonite RA, Ju
G. Molecular cloning and characterization of a second subunit of
the interleukin 1 receptor complex. J Biol Chem 1995;270:13757-
65
2. Huang J, Gao X, Li S, Cao Z. Recruitment of IRAK to the
interleukin 1 receptor complex requires interleukin 1 receptor
accessory protein. Proc Natl Acad Sci U S A 1997;94:12829-32
3. Wesche H, Korherr C, Kracht M, Falk W, Resch K, Martin MU.
The interleukin-1 receptor accessory protein (IL-1RAcP) is
essential for IL-1-induced activation of interleukin-1 receptorassociated
kinase (IRAK) and stress-activated protein kinases
(SAP kinases). J Biol Chem 1997;272:7727-31
4. Hofmeister R, Wiegmann K, Korherr C, Bernardo K, Kronke M,
Falk W. Activation of acid sphingomyelinase by interleukin-1 (IL-1)
requires the IL-1 receptor accessory protein. J Biol Chem
1997;272:27730-6
(RD1299)

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Suite 207
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www.prosci-inc.com
Toll Free: 888-513-9525
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techsupport@prosci-inc.com
Anti-IL-1RAcP (CT)
CATALOG No.: 2131
BACKGROUND:
The pro-inflammatory cytokine IL-1 induced cellular
response requires two subunits of its receptor, IL-1 receptor I
(IL-1RI) and IL-1 receptor accessory protein (IL-1RAcP) (1).
IL-1RAcP forms a complex with IL-1RI in response to IL-1
treatment. The IL-1 receptor-associated kinase (IRAK),
which mediates activation of NF-κB inducing kinae (NIK) and
of NF-κB, recruits to the IL-1R complex through IL-1RAcP
(2). IL-1 activation of stress-activated protein kinase and of
acid sphingomyelinase also requires IL-1RAcP (3,4). Like
IL-1RI, IL-1RAcP subunit is essential for IL-1 mediated
cellular response. IL-1RAcP is expressed in many tissues.
SOURCE:
Rabbit anti-IL-1RAcP (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 549 to 569
of human IL-1RAcP, which differs from the sequence of
mouse origin by three amino acids (1).
APPLICATION:
This polyclonal antibody can be used for detection of IL-
1RAcP by Western blot at 1:500 to 1:1000 dilution. Whole
lysate from HeLa cells can be used as positive control and
an approximately 66 kDa band can be detected. It has no
cross activity to other members in the IL-1 receptor family.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of IL-
1RAcP in HeLa whole cell
lysate with anti-IL-1RAcP
(CT) at 1:500 dilution.
REFERENCES:
1. Greenfeder SA, Nunes P, Kwee L, Labow M, Chizzonite RA, Ju
G. Molecular cloning and characterization of a second subunit of
the interleukin 1 receptor complex. J Biol Chem 1995;270:13757-
65
2. Huang J, Gao X, Li S, Cao Z. Recruitment of IRAK to the
interleukin 1 receptor complex requires interleukin 1 receptor
accessory protein. Proc Natl Acad Sci U S A 1997;94:12829-32
3. Wesche H, Korherr C, Kracht M, Falk W, Resch K, Martin MU.
The interleukin-1 receptor accessory protein (IL-1RAcP) is
essential for IL-1-induced activation of interleukin-1 receptorassociated
kinase (IRAK) and stress-activated protein kinases
(SAP kinases). J Biol Chem 1997;272:7727-31
4. Hofmeister R, Wiegmann K, Korherr C, Bernardo K, Kronke M,
Falk W. Activation of acid sphingomyelinase by interleukin-1 (IL-1)
requires the IL-1 receptor accessory protein. J Biol Chem
1997;272:27730-6
(RD1299)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-APP (Aβ-NT)
CATALOG NO.: 2133
BACKGROUND:
Accumulation of the amyloid-β peptide (Aβ) in the cerebral
cortex is a critical event in the pathogenesis of Alzheimer’s
disease. The β−amyloid protein precursor (APP) is cleaved
by β−secretase, producing a soluble derivative of the protein
and a membrane anchored 99-amino acid carboxy-terminal
fragment (C99). The C99 fragment serves as substrate for
γ−secretase to generate the 4 kDa amyloid-β peptide (Aβ),
which is deposited in the brains of all suffers of Alzheimer’s
disease.
SOURCE:
Rabbit anti-APP (Aβ-NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 653 to 662
of human amyloid A4 protein precursor (APP) (1) or 1 to 10
of the 4K Aβ peptide generated by β− and γ−secretases (2).
The peptide sequences are identical to those of rabbit, pig,
bovine, guinea pig, and chicken.
APPLICATION:
This polyclonal antibody can be used for detection of APP
and Aβ peptide by Western blot at 1:500 to 1:1000 dilution.
Murine brain lysate can be used as positive control. It is
human, mouse, and rat reactive. This antibody is for
research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 100 µg / 500 µl, is available for
competition studies (Catalog No. 2133P).
Murine brain tissue lysate, 500 µg / 200 µl, is available for
positive control (Catalog No. 1255).
Western blot analysis of APP
in human (A), mouse (B), and
rat (C) brain tissue lysates
with anti-APP (Aβ-NT) at
1:500 dilution.
REFERENCES:
1. Ponte P, Gonzalez-DeWhitt P, Schilling J, Miller J, Hsu D,
Greenberg B, Davis K, Wallace W, Lieberburg I, Fuller F. A new
A4 amyloid mRNA contains a domain homologous to serine
proteinase inhibitors. Nature 1988;331:525-7.
2. Selkoe D.J. Cell biology of the amyloid beta-protein precursor
and the mechanism of Alzheimer's disease. Annu Rev Cell Biol
1994;10:373-403
(RD1000)

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Anti-APP (CT)
CATALOG NO.: 2136
BACKGROUND:
Accumulation of the amyloid-β peptide (Aβ) in the cerebral
cortex is a critical event in the pathogenesis of Alzheimer’s
disease. The β−amyloid protein precursor (APP) is cleaved
by β−secretase, producing a soluble derivative of the protein
and a membrane anchored 99-amino acid carboxy-terminal
fragment (C99). The C99 fragment serves as substrate for
γ−secretase to generate the 4 kDa amyloid-β peptide (Aβ),
which is deposited in the brains of all suffers of Alzheimer’s
disease.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
Western blot analysis of
APP in mouse (M) and rat
(R) brain tissue lysates with
anti-APP (CT) at 1:500
dilution.
SOURCE:
Rabbit anti-APP (CT) polyclonal antibody was raised against
a peptide corresponding to amino acids 737 to 751 of human
amyloid A4 protein precursor (APP) (1) or 85 to 99 of the
C99 fragment generated by β− secretase cleavage (2). The
peptide sequences are identical to those of monkey, mouse,
rat, chicken, and a variety of other species.
APPLICATION:
This polyclonal antibody can be used for detection of APP
and the C99 fragment by Western blot at 1:500 to 1:1000
dilution. Murine brain lysate can be used as positive control.
It is human, mouse, and rat reactive. This antibody is for
research use only.
RELATED PRODUCTS:
Blocking peptide, 100 µg / 500 µl, is available for
competition studies (Catalog No. 2136P).
Murine brain tissue lysate, 500 µg / 200 µl, is available for
positive control (Catalog No. 1255).
REFERENCES:
1. Ponte P, Gonzalez-DeWhitt P, Schilling J, Miller J, Hsu D,
Greenberg B, Davis K, Wallace W, Lieberburg I, Fuller F. A new
A4 amyloid mRNA contains a domain homologous to serine
proteinase inhibitors. Nature 1988;331:525-7
2. Selkoe D.J. Cell biology of the amyloid beta-protein precursor
and the mechanism of Alzheimer's disease. Annu Rev Cell Biol
1994;10:373-403
(RD1299)

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Anti-DcR3 (NT) TR6
CATALOG No.: 2140
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand in the TNF family through their death domain
containing receptors. Several novel members in the TNFR
family including DR3, DR4, DR5, and DR6 were recently
discovered and function as cell death receptors. Two decoy
receptors, DcR1 and DcR2, were recently identified to
compete with DR4 and DR5 for their ligand TRAIL binding. A
novel decoy receptor was more recently discovered and
designated DcR3 and TR6, respectively, (1,2). Unlike DcR1
and DcR2, DcR3 is a soluble rather than a membrane
associated molecule. DcR3 binds to FasL and LIGHT and
inhibits FasL and LIGHT induced apoptosis (1,2). DcR3
transcript is expressed in a number of lung and colon
carcinomas and in some normal tissues.
SOURCE:
Rabbit anti-DcR3/TR6 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 31 to 46 of
human DcR3 precursor (1,2).
APPLICATION:
This polyclonal antibody can be used for detection of DcR3
expression by Western blot at 1:500 to 1:1000 dilution.
Tissue lysate of human heart can be used as positive control
and an approximately 33 kDa band can be detected. It is
human, mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at -20°C. Stable for one year at 2-8°C.
Western blot analysis of DcR3
in human heart (H), brain (B),
and kidney (K) tissue lysates
with anti-DcR3 (NT) at 1:500
dilution.
REFERENCES:
1. Pitti RM, Marsters SA, Lawrence DA, Roy M, Kischkel FC, Dowd
P, Huang A, Donahue CJ, Sherwood SW, Baldwin DT, Godowski
PJ, Wood WI, Gurney AL, Hillan KJ, Cohen RL, Goddard AD,
Botstein D, Ashkenazi A. Genomic amplification of a decoy
receptor for Fas ligand in lung and colon cancer. Nature
1998;396:699-703
2. Yu KY, Kwon B, Ni J, Zhai Y, Ebner R, Kwon BS. A newly
identified member of tumor necrosis factor receptor superfamily
(TR6) suppresses LIGHT-mediated apoptosis. J Biol Chem
1999;274:13733-6
(RD1299)

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Anti-SODD (NT)
CATALOG No.: 2143
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand of the TNF family through their death domain
containing receptors, TNF-R1 and Fas. Several novel death
receptors including DR3, DR4, DR5, and DR6 were recently
identified. Cell death signal is transduced by death domain
containing adapter molecules through the interaction with
death domain of these death receptors. A novel TNF-R1
interacting protein was recently identified and designated
SODD for silencer of death domains (1). SODD associates
with the death domain of TNF-R1 and prevents constitutive
activation of TNF-R1 signaling. TNF treatment releases
SODD and permits adapter molecules such as TRADD
recruiting to the active TNF-R1 complex, which activates
TNF signaling pathways. SODD also interacts with DR3.
SODD is ubiquitously expressed in human tissues and cell
lines.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of SODD
in HeLa (1,3) and THP-1 (2,4)
whole cell lysates in the
absence (1,2) or presence (3,4)
of blocking peptide (Catalog no.
2143P) with anti-SODD (NT) at
1:500 dilution.
REFERENCES:
1. Jiang Y, Woronicz JD, Liu W, Goeddel DY. Prevention of
constitutive TNF receptor 1 signaling by silencer of death domains.
Science 1999;283:543-6
(RD1299)
SOURCE:
Rabbit anti-SODD (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 2 to 16 of
human SODD (1).
APPLICATION:
This polyclonal antibody can be used for detection of SODD
by Western blot at 1:500 to 1:2000 dilution. HeLa and THP-1
whole cell lysate can be used as positive control and an
approximately 60 kDa band can be detected. It is human,
mouse, and rat reactive. For research use only.

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Anti-DRAK1 (NT)
CATALOG No.: 2147
BACKGROUND:
Apoptosis is mediated by death domain containing adapter
molecules and a caspase family of proteases. Certain
serine/threonine protein kinases, such as ASK-1 and RIP,
are mediators of apoptosis. Two novel serine/threonine
kinases that induce apoptosis were recently identified and
designated DRAK1 and DRAK2 for DAP kinase-related
apoptosis-inducing protein kinases (1). DRAKs contain an N-
terminal kinase domain and a C-terminal regulation domain.
Overexpression of DRAK1 induces apoptosis. DRAKs have
high sequence homology to DAP and ZIP kinases, and they
represent a novel family of serine/threonine kinases, which
mediates apoptosis through their catalytic activities. DRAK1
is located in nucleus and the messenger RNA was
ubiquitously expressed in human tissues (1).
SOURCE:
Rabbit anti-DRAK1 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 5 to 19 of
human DRAK1 (1).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
DRAK1 in MOLT4 (A),
A431 (B), and 3T3 (C)
whole cell lysates with
anti-DRAK1 (2147) at
1:500 dilution.
REFERENCES:
1. Sanjo H, Kawai T, Akira S. DRAKs, novel serine/threonine
kinases related to death-associated protein kinase that trigger
apoptosis. J Biol Chem 1998;273:29066-71
(WD1299)
APPLICATION:
This polyclonal antibody can be used for detection of DRAK1
by Western blot at 1:500 to 1:1000 dilution. A431 or MOLT4
whole cell lysate can be used as positive control and an
approximately 50 kDa band can be detected. It is human,
mouse, and rat reactive, and has no cross responses to
DRAK2, DAP or ZIP kinases. For research use only.

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Anti-DRAK2 (CT)
CATALOG No.: 2149
BACKGROUND:
Apoptosis is mediated by death domain containing adapter
molecules and a caspase family of proteases. Certain
serine/threonine protein kinases, such as ASK-1 and RIP,
are mediators of apoptosis. Two novel serine/threonine
kinases that induce apoptosis were recently identified and
designated DRAK1 and DRAK2 (for DAP kinase-related
apoptosis-inducing protein kinases) (1). DRAKs contain an
N-terminal kinase domain and a C-terminal regulation
domain. Overexpression of DRAK2 induces apoptosis.
DRAKs have high sequence homology to DAP and ZIP
kinases, and they represent a novel family of
serine/threonine kinases, which mediates apoptosis through
their catalytic activities. DRAK2 is located in nucleus and the
messenger RNA was ubiquitously expressed in human
tissues (1).
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of
DRAK2 in Jurkat (1,3) and
Raji (2,4) cell lysate in the
absence (1,2) or presence
(3,4) of blocking peptide with
anti-DRAK2 (CT) at 1:500
dilution.
REFERENCES:
1. Sanjo H, Kawai T, Akira S. DRAKs, novel serine/threonine
kinases related to death-associated protein kinase that trigger
apoptosis. J Biol Chem 1998;273:29066-71
(RD1299)
SOURCE:
Rabbit anti-DRAK2 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 351 to 365
of human DRAK2 (1).
APPLICATION:
This polyclonal antibody can be used for detection of DRAK2
by Western blot at 1:500 to 1:1000 dilution. Whole cell lysate
from Jurkat cells can be used as positive control and an
approximately 45 kDa band can be detected. It has no cross
responses to DAP or ZIP kinases. The approximately 70 kDa
band is probably non-related to DRAK2 although it is peptide
blockable. For research use only.

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Anti-DFF40 (NT) CPAN, hCAD
CATALOG No.: 2153
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A mouse DNase
that causes DNA fragmentation was identified recently and
designated CAD for caspase activated deoxyribonuclease
(1,2). The human homologue of mouse CAD was more
recently identified by three groups independently and termed
CPAN, DFF40, and human CAD, respectively, (3-5).
DFF45/ICAD is the inhibitory protein of DFF40/CAD (1,2,6)
and forms complex with DFF40/CAD. Upon cleavage of
DFF45/ICAD by activated caspase, DFF40/CAD is released
and activated and eventually causes the degradation of DNA
in the nuclei. Activation of DFF40/CAD, which causes DNA
degradation, is the hallmark of apoptotic cell death.
SOURCE:
Rabbit anti-DFF40 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 3 to 18 of
human DFF40 (4, 5).
APPLICATION:
This polyclonal antibody can be used for detection of DFF40
by Western blot at 1:500 to 1:2000 dilution. K562 or Jurkat
whole cell lysate can be used as positive control and a 40
kDa band can be detected. It is human and mouse reactive.
For research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100 µg
in 200 µl of PBS containing 0.02% sodium azide. Store at
4°C, stable for one year.
Western blot analysis of
DFF40 in Jurkat (J) and
K562 (K) whole cell lysate
with anti-DFF40 (NT) at
1:500 dilution.
REFERENCES:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
2. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
3. Halenbeck R, MacDonald H, Roulston A, Chen TT, Conroy L,
Williams LT. CPAN, a human nuclease regulated by the caspasesensitive
inhibitor DFF45. Curr Biol 1998;8:537-40
4. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
5. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H,
Nagata S. Molecular cloning and characterization of human
caspase-activated DNase. Proc Natl Acad Sci USA 1998;95:9123-
8
6. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
(WD1299)

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Anti-DFF40 (IN) CPAN, hCAD
CATALOG No.: 2155
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain containing adapter
molecules and members of the caspase family of proteases.
These death signals finally cause the degradation of
chromosomal DNA by activated DNase. A mouse DNase
that causes DNA fragmentation was identified recently and
designated CAD for caspase activated deoxyribonuclease
(1,2). The human homologue of mouse CAD was more
recently identified by three groups independently and termed
CPAN, DFF40, and human CAD, respectively, (3-5).
DFF45/ICAD is the inhibitory protein of DFF40/CAD (1,2,6)
and forms complex with DFF40/CAD. Upon cleavage of
DFF45/ICAD by activated caspase, DFF40/CAD is released
and activated and eventually causes the degradation of DNA
in the nuclei. Activation of DFF40/CAD, which causes DNA
degradation, is the hallmark of apoptotic cell death.
SOURCE:
Rabbit anti-DFF40 (IN) polyclonal antibody was raised
against a peptide corresponding to amino acids 203 to 218
of human DFF40 (4, 5).
APPLICATION:
This polyclonal antibody can be used for detection of DFF40
/CAD by Western blot at 1:500 dilution. K562 or Jurkat whole
cell lysate can be used as positive control and a 40 kDa
band can be detected. It is human, mouse, and rat reactive,
For research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100
µg in 200 µl of PBS containing 0.02% sodium azide. Store
at 4°C, stable for one year.
REFERENCES:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A,
Nagata S. A caspase-activated DNase that degrades DNA during
apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50
2. Sakahira H, Enari M, Nagata S. Cleavage of CAD inhibitor in
CAD activation and DNA degradation during apoptosis. Nature
1998;391:96-99
3. Halenbeck R, MacDonald H, Roulston A, Chen TT, Conroy L,
Williams LT. CPAN, a human nuclease regulated by the caspasesensitive
inhibitor DFF45. Curr Biol 1998;8:537-40
4. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The
40-kDa subunit of DNA fragmentation factor induces DNA
fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
5. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H,
Nagata S. Molecular cloning + characterization of human caspaseactivated
DNase. Proc Natl Acad Sci USA 1998;95:9123-8
6. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric
protein that functions downstream of caspase-3 to trigger DNA
fragmentation during apoptosis. Cell 1997;89:175-184
(WD0300)

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Anti-DR6 (NT)
CATALOG No.: 2157
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand of the TNF family through their death domain
containing receptors, TNF-R1 and Fas. Several novel death
receptors including DR3, DR4, and DR5 were recently
identified. A new death domain containing receptor in the
TNFR family was cloned recently and termed DR6 for death
receptor-6 (1). Like TNF-R1, DR6 interacts with death
domain containing adapter molecule TRADD.
Overexpression of DR6 induces apoptosis and activates NFκB
and JNK. DR6 is widely expressed in human tissues and
cell lines (1). The ligand for DR6 has not been identified.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
Western blot analysis of DR6
in K562 (1,3) and Raji (2,4)
whole cell lysate in the
absence (1,2) or presence
(3,4) of blocking peptide
(Catalog no. 2157P) with anti-
DR6 (NT) at 1:500 dilution.
SOURCE:
Rabbit anti-DR6 (NT) polyclonal antibody was raised against
a peptide corresponding to amino acids 42 to 56 of human
DR6 precursor (1).
APPLICATION:
This polyclonal antibody can be used for detection of DR6 by
Western blot at 1:500 to 1:2000 dilution. HeLa and K562
whole cell lysate can be used as positive control and an
approximately 68 kDa band can be detected. For research
use only.
REFERENCES:
1. Pan G, Bauer JH, Haridas V, Wang S, Liu D, Yu G, Vincenz C,
Aggarwal BB, Ni J, Dixit VM. Identification and functional
characterization of DR6, a novel death domain-containing TNF
receptor. FEBS Lett 1998;431:351-6
(RD1299)

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Anti-Bcl10 (NT) CIPER, mE10, CARMEN, CLAP
CATALOG No.: 2161
BACKGROUND:
Apoptosis is related to many diseases including cancer. Cell
death signals are transduced by death domain (DD) and
caspase recruitment domain (CARD) containing molecules
and a caspase family of proteases. CARD containing cell
death regulators include ARC, RAIDD, Apaf-1, caspase-9,
and caspase-2. A novel CARD containing protein was
recently identified by several groups and designated Bcl10,
CIPER, mE10, CARMEN, CLAP (1-6). Bcl10 is a cellular
homolog of the equine herpesvirus-2 E-10 gene.
Overexpression of Bcl10 induces JNK, p38, and NF-κB
activation (1,2,4,6). Bcl10 interacts with caspase-9 and
enhances pro-caspase-9 processing (3) and induces
apoptosis through caspase-9 activation (3.6). Bcl10 exhibits
a variety of mutations in MALT lymphomas and in B and T
cell lineage lymphomas indicating that it may be commonly
involved in the pathogenesis of human malignancy (1,5).
Bcl10 is expressed in many human and murine tissues and
cell lines (2-6).
SOURCE:
Rabbit anti-BCL10 (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 5 to 19 of
human origin (1-6).
APPLICATION:
This polyclonal antibody can be used for detection of BCL10
by Western blot at 1:500 dilution. Raji whole cell lysate can
be used as positive control and an approximately 31 kDa
band can be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2161P).
Raji cell lysate, 200 µg/100 µl, is available for positive
control (Catalog No. 1207).
Western blot analysis of Bcl-10
in Raji whole cell lysate in the
absence (A) or presence (B) of
peptide (2161P) with anti-Bcl-10
(NT) at 1:500 dilution.
REFERENCES:
1. Willis TG, Jadayel DM, Du MQ, et al. Bcl10 is involved in
t(1;14)(p22;q32) of MALT B cell lymphoma and mutated in multiple
tumor types. Cell 1999;96(1):35-45
2. Koseki T, Inohara N, Chen S, et al. CIPER, a novel NF kappaBactivating
protein containing a caspase recruitment domain with
homology to Herpesvirus-2 protein E10. J Biol Chem
1999;274(15):9955-61
3. Yan M, Lee J, Schilbach S, Goddard A, Dixit V. mE10, a novel
caspase recruitment domain-containing proapoptotic molecule. J
Biol Chem 1999;274(15):10287-92
4. Thome M, Martinon F, Hofmann K, et al. Equine herpesvirus-2
E10 gene product, but not its cellular homologue, activates NFkappaB
transcription factor and c-Jun N-terminal kinase. J Biol
Chem 1999;274(15):9962-8
5. Zhang Q, Siebert R, Yan M, Hinzmann B, et al. Inactivating
mutations and overexpression of BCL10, a caspase recruitment
domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32).
Nat Genet 1999;22(1):63-8
6. Srinivasula SM, Ahmad M, Lin JH, et al. CLAP, a novel caspase
recruitment domain-containing protein in the tumor necrosis factor
receptor pathway, regulates NF-kappaB activation and apoptosis. J
Biol Chem 1999;274(25):17946-54
(WD0300)

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Anti-DcR1 (ED) TRAIL-R3, TRID, LIT
CATALOG No.: 2179
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand in the TNF family through their death domain
containing receptors. TRAIL/Apo2L is a new member of the
TNF family and induces apoptosis of a variety of tumor cell
lines. DR4 and DR5 are the recently identified functional
receptors for TRAIL (1-3). Two decoy receptors for TRAIL
have been identified and designated DcR1/TRID/TRAIL-
R3/LIT (2-7) and DcR2/TRAIL-R4/TRUNDD (8-10). DcR1
has extracellular TRAIL-binding domain but lacks
intracellular signaling domain. It is a glycophospholipidanchored
cell surface protein. DcR1 transcripts were
expressed in many normal human tissues but not in most
cancer cell lines (2,3). Overexpression of DcR1 did not
induce apoptosis, but attenuated TRAIL-induced apoptosis
(2,3).
SOURCE:
Rabbit anti-DcR1 (ED) polyclonal antibody was raised
against a peptide corresponding to amino acids 149 to 167
at extracellular domain (ED) of human DcR1 precursor (2-3).
APPLICATION:
This polyclonal antibody can be used for detection of DcR1
by Western blot at 1:500 to 1:1000 dilution. HeLa cell lysate
can be used as positive control and an approximate 65 kDa
band can be detected (6). It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as chromatography purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at -20°C.
Stable for one year at 2-8°C.
Western blot analysis of DcR1
in HeLa whole cell lysate with
anti-DcR1 (ED) at 1:500 dilution.
REFERENCES:
1. Pan G; O'Rourke K; Chinnaiyan et al.. The receptor for the cytotoxic
ligand TRAIL. Science; 1997;276:111-113
2. Pan G, Ni J, Wei YF, et al. An antagonist decoy receptor and a death
domain-containing receptor for TRAIL. Science 1997;277:815-8
3. Sheridan JP, Marsters SA, Pitti RM, et al. A. Control of TRAIL-induced
apoptosis by a family of signaling and decoy receptors. Science
1997;277:818-21
4. Degli-Esposti MA, Smolak PJ, Walczak H, et al, Smith CA. Cloning and
characterization of TRAIL-R3, a novel member of the emerging TRAIL
receptor family. J Exp Med 1997;186(7):1165-70
5. MacFarlane M, Ahmad M, Srinivasula SM, et al. Identification and
molecular cloning of two novel receptors for the cytotoxic ligand TRAIL. J
Biol Chem 1997;272(41):25417-20
6. Schneider P, Bodmer JL, Thome M, Hofmann K, Holler N, Tschopp J.
Characterization of two receptors for TRAIL. FEBS Lett 1997;416(3):329-34
7. Mongkolsapaya J, Cowper AE, Xu XN, et al. Lymphocyte inhibitor of
TRAIL (TNF-related apoptosis -inducing ligand): a new receptor protecting
lymphocytes from the death ligand TRAIL. J Immunol 1998;160(1):3-6
8. Marsters SA, Sheridan JP, Pitti RM, et al. A novel receptor for
Apo2L/TRAIL contains a truncated death domain. Curr Biol 1997;7:1003-6
9. Degli-Esposti MA, Dougall WC, Smolak PJ, et al. The novel receptor
TRAIL-R4 induces NF-kappaB and protects against TRAIL-mediated
apoptosis, yet retains an incomplete death domain. Immunity 1997;7:813-20
10. Pan G, Ni J, Yu G, et al. TRUNDD, a new member of the TRAIL
receptor family that antagonizes TRAIL signalling. FEBS Lett 1998;424:41-5
(RD0800)

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Anti-RICK (CT) RIP2, CARDIAK
CATALOG No.: 2183
BACKGROUND:
Apoptosis is mediated by death domain (DD) and/or caspase
recruitment domain (CARD) containing molecules and a
caspase family of proteases. DD-containing serine/threonine
kinase RIP regulates Fas-induced apoptosis. A novel CARDcontaining
serine/threonine kinase was recently identified
and designated RICK/RIP2/CARDIAK for RIP-like interacting
CLARP kinase, receptor interacting protein-2, and CARDcontaining
ICE associated kinase, respectively, (1-3). RICK
contains an N-terminal kinase catalytic domain and a C-
terminal CARD domain. Overexpression of RICK induced
apoptosis and activation of NF-κB and JNK. RICK interacts
with members of the TRAF family, CLARP and caspase-1.
Thus, RICK represents a novel kinase that regulates TNF
and Fas induced-apoptosis and that is involved in the
generation of proinflammatory cytokine IL-1β. The
messenger RNA of RICK is expressed in multiple human
tissues (1).
APPLICATION:
This polyclonal antibody can be used for detection of RICK
by Western blot at 1:500 dilution. K562 or 3T3 whole cell
lysate can be used as positive control and an approximately
60 kDa band can be detected. It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
REFERENCES:
1. Inohara N, del Peso L, Koseki T, Chen S, Nunez G. RICK, a
novel protein kinase containing a caspase recruitment domain,
interacts with CLARP and regulates CD95-mediated apoptosis. J
Biol Chem 1998;273:12296-300
2. McCarthy JV, Ni J, Dixit VM. RIP2 is a novel NF-kappaBactivating
and cell death-inducing kinase. J Biol Chem
1998;273:16968-75
SOURCE:
Rabbit anti-RICK (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 508 to 522
of human origin (1).
3. Thome M, Hofmann K, Burns K, Martinon F, Bodmer JL,
Mattmann C, Tschopp J. Identification of CARDIAK, a RIP-like
kinase that associates with caspase-1. Curr Biol 1998;8:885-8
(WD0300)

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Anti-ARC (NT)
CATALOG No.: 2185
BACKGROUND:
Apoptosis is regulated by death domain (DD) and/or
caspase recruitment domain (CARD) containing molecules
and a caspase family of proteases. CARD containing cell
death regulators include RAIDD, RICK BCL10, Apaf-1,
caspase-9, and caspase-2. A novel CARD domain
containing protein was recently identified and designated
ARC for apoptosis repressor with CARD (1). ARC interacts
with caspase-2 and –8 and inhibits enzymatic activity of
caspase-8. ARC suppresses apoptosis induced by cell death
adapters FADD and TRADD and by cell death receptors
Fas, TNFR-1, and DR3. The messenger RNA of ARC is
primarily expressed in skeletal muscle and cardiac tissue (1).
SOURCE:
Rabbit anti-ARC (NT) polyclonal antibody was raised against
a peptide corresponding to amino acids 2 to 18 of human
origin (1). These sequences are identical to those of human
nuclear protein Nop30 (2) and differ from those of the rat
homolog of ARC by one amino acid (3)
APPLICATION:
This polyclonal antibody can be used for detection of ARC
by Western blot at 1:500 dilution. Whole cell lysate from
HeLa cells can be used as positive control and an
approximately 25 kDa band can be detected. It is human,
mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2185P).
HeLa cell lysate, 200 µg/100 µl, is available for positive
control (Catalog No. 1201).
Western blot analysis of ARC in
HeLa whole cell lysates with anti-
ARC (NT) at 1:500 dilution.
REFERENCES:
1. Koseki T, Inohara N, Chen S, Nunez G. ARC, an inhibitor of
apoptosis expressed in skeletal muscle and heart that interacts
selectively with caspases. Proc Natl Acad Sci USA 1998;95:5156-
60
2. Stoss O, Schwaiger FW, Cooper TA, Stamm S. Alternative
splicing determines the intracellular localization of the novel
nuclear protein Nop30 and its interaction with the splicing factor
SRp30c. J Biol Chem 1999;274(16):10951-62
3. Geertman R, McMahon A, Sabban EL. Cloning and
characterization of cDNAs for novel proteins with glutamic acidproline
dipeptide tandem repeats. Biochim Biophys Acta
1996;1306(2-3):147-52
(WD 0300)

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Anti-CX 3 CR1 (EL) V28, CMKBRL1
CATALOG No.: 2201
BACKGROUND:
CX 3 CR1 is one of the chemokine receptors that are required
as coreceptors for HIV infection. The genes encoding
human, mouse, and rat CX 3 CR1 were cloned and
designated V28 and CMKBRL1, CX 3 CR1, and RBS11,
respectively, (1-4). The encoded seven transmembrane
protein was recently identified as the receptor for a novel
transmembrane molecule, fractalkine, and renamed CX 3 CR1
(5). Recently, CX 3 CR1 was found to serve as a coreceptor
for HIV-1 and HIV-2 envelope fusion and virus infection,
which can be inhibited by fractokine (6). CX 3 CR1 mediates
leukocyte migration and adhesion (5). CX 3 CR1 is expressed
in a variety of human tissues and cell lines (2).
SOURCE:
Rabbit anti-CX 3 CR1 polyclonal antibody was raised against
a peptide corresponding to amino acids 175 to 189 of human
CX 3 CR1 (1,2). The sequence is identical to that of rat
CX 3 CR1 and differs from that of mouse CX 3 CR1 by one
amino acid (3,4).
APPLICATION:
This polyclonal antibody can be used for detection of
CX 3 CR1 by Western blot at 1:500 dilution. THP-1 cell lysate
can be used as positive control and an approximately 50
kDa band can be detected. For research use only.
STORAGE:
It is supplied as 100 µg of immunoaffinity chromatography
purified IgG in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2201P).
THP-1 cell lysate, 200 µg/100 µl, is available for positive
control (Catalog No. 1208).
Western blot analysis of
CX 3 CR1 in THP-1 cell lysate in
the absence (lane A) or
presence (lane B) of blocking
peptide with anti-CX 3 CR1 (EL)
at 1:500 dilution.
REFERENCES:
1. Raport CJ, Schweickart VL, Eddy RL JR, Shows TB, Gray PW. The
orphan G-protein-coupled receptor-encoding gene V28 is closely related to
genes for chemokine receptors and is expressed in lymphoid and neural
tissues. Gene 1995;163:295-9
2. Combadiere C, Ahuja SK, Murphy PM. Cloning, chromosomal localization,
and RNA expression of a human beta chemokine receptor-like gene. DNA
Cell Biol 1995;14:673-80
3. Combadiere C, Gao J, Tiffany HL, Murphy PM. Gene cloning, RNA
distribution, and functional expression of mCX3CR1, a mouse chemotactic
receptor for the CX3C chemokine fractalkine. Biochem Biophys Res
Commun 1998;253:728-32
4. Harrison JK, Barber CM, Lynch KR. cDNA cloning of a G-protein-coupled
receptor expressed in rat spinal cord and brain related to chemokine
receptors. Neurosci Lett 1994;169:85-9
5. Imai T, Hieshima K, Haskell C, et al. Identification and molecular
characterization of fractalkine receptor CX3CR1, which mediates both
leukocyte migration and adhesion. Cell 1997;91:521-30
6. Combadiere C, Salzwedel K, Smith ED, et al. Identification of CX3CR1. A
chemotactic receptor for the human CX3C chemokine fractalkine and a
fusion coreceptor for HIV-1. J Biol Chem 1998;273:23799-804 (RD0400)

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Anti-Bonzo (NT2) STRL33, TYMSTR
CATALOG NO.: 2209
BACKGROUND:
Human immunodeficiency virus (HIV) and simian
immunodeficiency virus (SIV) require coreceptors, in addition
to CD4, to infect target cells. Some G protein-coupled
receptors including CCR5, CXCR4, CCR3, and CCR2b in
the chemokine receptor family have been identified as HIV
coreceptors. An orphan G protein-coupled receptor was
recently cloned and designated Bonzo, STRL33 and
TYMSTR, and identified as HIV and SIV coreceptor (1-4).
Bonzo/STRL33 serves as coreceptor for SIV, HIV-2 and
HIV-1. The messenger RNA of Bonzo/STRL33 is expressed
in lymphoid tissues and activated peripheral blood
lymphocytes.
SOURCE:
Rabbit anti-Bonzo polyclonal antibody was raised against a
peptide corresponding to amino acids 11 to 25 of human
Bonzo/STRL33 (1,2). The sequence of this peptide differs
from those of African green monkey and pig-tailed macaque
by one or two amino acids, respectively, (1).
APPLICATION:
This polyclonal antibody can be used for detection of Bonzo
by Western blot at 1:500 dilution. Human spleen tissue
lysate can be used as positive control. For research use
only.
STORAGE:
It is supplied as 100 µg of immunoaffinity purified IgG in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2209P).
Human spleen tissue lysate, 200 µg/100 µl, is available for
positive control (Catalog No. 1306).
Western blot analysis of
Bonzo in human spleen tissue
lysate in the absence (lane A)
or presence (lane B) of
peptide with anti-Bonzo (NT2)
at 1:500 dilution.
REFERENCES:
1. Deng HK, Unutmaz D, KewalRamani VN, Littman DR.
Expression cloning of new receptors used by simian and human
immunodeficiency viruses. Nature 1997;388:296-300
2. Liao F, Alkhatib G, Peden KW, Sharma G, Berger EA, Farber
JM. STRL33, A novel chemokine receptor-like protein, functions as
a fusion cofactor for both macrophage-tropic and T cell line-tropic
HIV-1. J Exp Med 1997;185:2015-23
3. Alkhatib G, Liao F, Berger EA, Farber JM, Peden KW. A new
SIV co-receptor, STRL33. Nature 1997;388:238
4. Loetscher M, Amara A, Oberlin E, Brass N, Legler D, Loetscher
P, D'Apuzzo M, Meese E, Rousset D, Virelizier JL, Baggiolini M,
Arenzana-Seisdedos F, Moser B. TYMSTR, a putative chemokine
receptor selectively expressed in activated T cells, exhibits HIV -1
coreceptor function. Curr Biol 1997;7:652-60 (RD0400)

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Anti-IRAK2 (CT)
CATALOG No.: 2213
BACKGROUND:
The pro-inflammatory cytokine IL-1 induces cellular response
through two subunits of its receptor, IL-1 receptor I (IL-1RI)
and IL-1 receptor accessory protein (IL-1RAcP). IL-1
receptor-associated kinase (IRAK) mediates activation of
NF-κB (1), which is a pivotal transcription factor mediating
inflammatory and immune response. A novel member in the
IRAK/Pelle family was recently identified and designated
IRAK2 (2). Both IRAK and IRAK2 recruit to the subunits of
the IL-1R complex after IL-1 binding and lead to NF-κB
activation. IRAKs also associate with Toll-like receptor (TLR)
and the dominant negative mutants of IRAKs inhibit LPSinduced
NF-κB activation (3,4). Members in IRAK/Pelle
family play a central role in IL-1R and TLR mediated
inflammatory responses to cytokine IL-1 and LPS. IRAK2 is
expressed in a variety of human tissues.
SOURCE:
Rabbit anti-IRAK2 (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 571 to 590
of human IRAK2 (2).
APPLICATION:
This polyclonal antibody can be used for detection of IRAK2
by Western blot at 1:500 to 1:1000 dilution. K562 whole cell
lysate can be used as positive control and a 65 kDa band
can be detected. Anti-IRAK2 has no cross response to IRAK.
For research use only.
STORAGE:
It is supplied as chromatography purified IgG, 100 µg in
200 µl of PBS containing 0.02% sodium azide. Store at
4°C, stable for one year.
Western blot analysis of
IRAK2 in K562 whole cell
lysate with anti-IRAK2 (CT) at
1:500 dilution.
REFERENCES:
1. Cao Z; Henzel WJ; Gao X. IRAK: a kinase associated with the
interleukin-1 receptor. Science 1996;271:1128-31.
2. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member
IRAK-2 and MyD88 as proximal mediators of IL-1 signaling.
Science 1997;278:1612-5
3. Zhang FX, Kirschning CJ, Mancinelli R, Xu XP, Jin Y, Faure E,
Mantovani A, Rothe M, Muzio M, Arditi M. Bacterial
lipopolysaccharide activates nuclear factor-kappaB through
interleukin-1 signaling mediators in cultured human dermal
endothelial cells and mononuclear phagocytes. J Biol Chem
1999;274:7611-4
4. Yang RB, Mark MR, Gurney AL, Godowski PJ. Signaling events
induced by lipopolysaccharide-activated toll-like receptor 2. J
Immunol 1999;163:639-43
(RD0300)

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Anti-Acinus (CP)
CATALOG No.: 2215
BACKGROUND:
Chromatin condensation and nuclear fragmentation (CCNF)
is the hallmark of apoptosis. CCNF is triggered by the
activation of members of caspase family, caspase activated
DNase (CAD/DFF40), and several novel proteins including
AIF and CIDE (1). A new inducer of chromatin condensation
was recently identified and designated Acinus (for apoptotic
chromatin condensation inducer in the nucleus). Acinus is
cleaved by caspase-3 and an additional unknown protease
generating a small active peptide p17, which causes
chromatin condensation in vitro when it is added to purified
nuclei. Acinus also induces apoptotic chromatin
condensation in cells. Acinus is ubiquitously expressed.
Three different spliced forms of Acinus have been identified
in human and mouse and designated AcinusL, AcinusS and
AcinusS’ (2).
SOURCE:
Rabbit anti-Acinus (CP) polyclonal antibody was raised
against a peptide (TRTALHGVKWPQSNPK) corresponding
to amino acids 1065 to 1080 of human AcinusL, 338 to 353
of human AcinusS’, or 307 to 322 of human AcinusS, which
are identical to those of mouse Acinus (2). The selected
antigenic sequence is located near the C-terminus of the
cleaved active peptide p17.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
RELATED PRODUCTS:
Western blot analysis of Acinus in
K562 whole cell lysate with anti-
Acinus (CP) at 1 µg/ml.
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2215P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death.
Nature 1999 ;401:127-8.
2. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto
Y. Acinus is a caspase-3-activated protein required for apoptotic
chromatin condensation. Nature 1999 401:168-73.
(WD0800)
APPLICATION:
This polyclonal antibody can be used for detection of Acinus
by Western blot at 0.5 to 1 µg/ml. K562 cell lysate can be
used as positive control and an approximate 220 kDa band
can be detected. For research use only.

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Anti-Acinus (CT)
CATALOG No.: 2217
BACKGROUND:
Chromatin condensation and nuclear fragmentation (CCNF)
is the hallmark of apoptosis. CCNF is triggered by the
activation of members of caspase family, caspase activated
DNase (CAD/DFF40), and several novel proteins including
AIF and CIDE (1). A new inducer of chromatin condensation
was recently identified and designated Acinus (for apoptotic
chromatin condensation inducer in the nucleus). Acinus is
cleaved by caspase-3 and an additional unknown protease
generating a small active peptide p17, which causes
chromatin condensation in vitro when it is added to purified
nuclei. Acinus also induces apoptotic chromatin
condensation in cells. Acinus is ubiquitously expressed.
Three different spliced forms of Acinus have been identified
in human and mouse and designated AcinusL, AcinusS and
AcinusS’ (2).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
Acinus in K562 whole cell
lysate with anti-Acinus (CT) at
0.5 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2217P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
SOURCE:
Rabbit anti-Acinus (CT) polyclonal antibody was raised
against a peptide (SRSTPVRDRGGRR) corresponding to
amino acids 1329 to 1341 of human AcinusL, 602 to 614 of
human AcinusS’, or 571 to 583 of human AcinusS, which are
identical to those of mouse Acinus (2).
APPLICATION:
This polyclonal antibody can be used for detection of Acinus
by Western blot at 0.25 to 0.5 µg/ml. K562 cell lysate can be
used as positive control and an approximate 220 kDa band
can be detected. For research use only.
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death.
Nature 1999 ;401:127-8.
2. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto
Y. Acinus is a caspase-3-activated protein required for apoptotic
chromatin condensation. Nature 1999 401:168-73.
(WD0800)

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Anti-Acinus (IN)
CATALOG No.: 2219
BACKGROUND:
Chromatin condensation and nuclear fragmentation (CCNF)
is the hallmark of apoptosis. CCNF is triggered by the
activation of members of caspase family, caspase activated
DNase (CAD/DFF40), and several novel proteins including
AIF and CIDE (1). A new inducer of chromatin condensation
was recently identified and designated Acinus (for apoptotic
chromatin condensation inducer in the nucleus). Acinus is
cleaved by caspase-3 and an additional unknown protease
generating a small active peptide p17, which causes
chromatin condensation in vitro when it is added to purified
nuclei. Acinus also induces apoptotic chromatin
condensation in cells. Acinus is ubiquitously expressed.
Three different spliced forms of Acinus have been identified
in human and mouse and designated AcinusL, AcinusS and
AcinusS’ (2).
SOURCE:
Rabbit anti-Acinus (IN) polyclonal antibody was raised
against a peptide (DTSENRPENDVPEPP) corresponding to
amino acids 775 to 789 of human AcinusL, 48 to 62 of
human AcinusS’, or 17 to 31 of human AcinusS, which differ
from those of mouse Acinus by one amino acid (2).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of Acinus
in K562 whole cell lysate with
anti-Acinus (IN) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2219P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death.
Nature 1999 ;401:127-8.
2. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto
Y. Acinus is a caspase-3-activated protein required for apoptotic
chromatin condensation. Nature 1999 401:168-73.
(WD0800)
APPLICATION:
This polyclonal antibody can be used for detection of Acinus
by Western blot at 0.5 to 1 µg/ml. K562 cell lysate can be
used as positive control and an approximate 220 kDa band
can be detected. For research use only.

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Anti-BAFF (CT) BLyS, TALL-1, THANK
CATALOG No.: 2221
BACKGROUND:
Members in the TNF superfamily regulate immune
responses and induce apoptosis. A novel member in the
TNF family was recently identified by several groups and
designated BAFF (for B cell Activating Factor belonging to
the TNF Family), BLyS (for B Lymphocyte Stimulator), TALL-
1 (for TNF- and ApoL-related Leukocyte-expressed Ligand),
and THANK (for TNF Homologue that Activate Apoptosis,
NF-κB and c-jun N-terminal Kinase) (1-4). BAFF/BLyS was
characterized as a B cell stimulator since it induced B cell
proliferation and immunoglobulin secretion (1,2). Two
receptors for BAFF were recently identified and designated
TACI and BCMA (5). BAFF and its receptors are involved in
the development of systemic lupus erythaematosus and
other B cell associated autoimmune diseases (5,6). Like
TNFα and TRAIL, THANK was shown to activate NF-κB and
c-jun N-terminal kinase (JNK) and to induce apoptosis (4).
SOURCE:
Rabbit anti-BAFF (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 254 to 269
of human BAFF (1-4).
APPLICATION:
This polyclonal antibody can be used for detection of BAFF
by Western blot at 0.25 to 1 µg/ml. It is human, mouse and
rat reactive. For research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year. Azide free antibody is
available.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2221P).
HL60 cell lysate, 200 µg/100 µl, is available for positive
control (Catalog No. 1209).
Western blot analysis of
BAFF in human HL60 cell
lysate (A) and murine spleen
tissue lysate (B) with anti-
BAFF (CT) at 1 µg/ml.
REFERENCES:
1. Moore PA, Belvedere O, Orr A, et al. BLyS: member of the
tumor necrosis factor family and B lymphocyte stimulator. Science
1999;285:260-3
2. Schneider P, MacKay F, Steiner V, et al. BAFF, a novel ligand of
the tumor necrosis factor family, stimulates B cell growth. J Exp
Med 1999;189:1747-56
3. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the
TNF family that is down-regulated by mitogens. J Leukoc Biol
1999;65:680-3
4. Mukhopadhyay A, Ni J, Zhai Y, Yu GL, Aggarwal BB.
Identification and characterization of a novel cytokine, THANK, a
TNF homologue that activates apoptosis, nuclear factor-kappaB,
and c-Jun NH2-terminal kinase. J Biol Chem 1999 ;274:15978-81
5. Gross JA, Johnston J, Mudri S, et al. TACI and BCMA are
receptors for a TNF homologue implicated in B-cell autoimmune
disease. Nature 2000;404:995-9
6. Khare SD, Sarosi I, Xia XZ, et al. Severe B cell hyperplasia and
autoimmune disease in TALL-1 transgenic mice. Proc Natl Acad
Sci USA 2000;97:3370-5
(WD0500)

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Anti-APRIL (ED) TALL-2, TRDL-1
CATALOG No.: 2223
BACKGROUND:
Members in the TNF superfamily regulate immune
responses and induce apoptosis. A novel member in the
TNF family was recently identified by several groups and
designated APRIL (for a proliferation-inducing ligand), TALL-
2 (for TNF- and ApoL-related Leukocyte-expressed Ligand
2), and TRDL-1α (for TNF related death ligand 1α) in human
and mouse (1-4). Two receptors for APRIL were recently
identified and designated TACI and BCMA (5-7). APRIL
stimulates B and T cell proliferation, triggers humoral
immune responses, activates NF-kB, and induces cell death
(1-7). APRIL and its close relative of BlyS and their
receptors BCMA and TACI are involved in diseases of
autoimmunity and cancer (8,9).
REFERENCES:
1. Hahne M, Kataoka T, Schroter M, et al. APRIL, a new ligand of
the tumor necrosis factor family, stimulates tumor cell growth. J
Exp Med. 1998;188(6):1185-90.
2. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the
TNF family that is down-regulated by mitogens. J Leukoc Biol.
1999;65(5):680-3.
3. Kelly K, Manos E, Jensen G, et al. APRIL/TRDL-1, a tumor
necrosis factor-like ligand, stimulates cell death. Cancer Res.
2000;60(4):1021-7.
4. Yu G, Boone T, Delaney J, et al. APRIL and TALL-I and
receptors BCMA and TACI: system for regulating humoral
immunity. Nat Immunol. 2000;1(3):252-6.
SOURCE:
Rabbit anti-APRIL (ED) polyclonal antibody was raised
against a synthetic peptide (GTGGPSQNGEGYP)
corresponding to amino acids 67 to 79 of human APRIL (1-
3).
APPLICATION:
This antibody can be used for detection of APRIL by
Western blot at 4-5 µg/ml. HL60 or Jurkat cell lysate can be
used as positive control and an approximately 42 kDa band
can be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2223P).
5. Wu Y, Bressette D, Carrell JA, et a. Tumor necrosis factor
(TNF) receptor superfamily member TACI is a high affinity receptor
for TNF family members APRIL and BLyS. J Biol Chem.
2000;275(45):35478-85.
6. Marsters SA, Yan M, Pitti RM, et al. Interaction of the TNF
homologues BLyS and APRIL with the TNF receptor homologues
BCMA and TACI. Curr Biol. 2000;10(13):785-8.
7. Rennert P, Schneider P, Cachero TG, at al. A soluble form of B
cell maturation antigen, a receptor for the tumor necrosis factor
family member APRIL, inhibits tumor cell growth. J Exp Med.
2000;192(11):1677-84.
8. Gross JA, Johnston J, Mudri S, et al. TACI and BCMA are
receptors for a TNF homologue implicated in B-cell autoimmune
disease. Nature 2000;404:995-9
9. Ware CF. APRIL and BAFF connect autoimmunity and cancer. J
Exp Med. 2000;192(11):F35-8.
(WD0105)

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Anti-DEDAF
CATALOG No.: 2227
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death
signals are transduced by death domain (DD) death effector
domain (DED), and caspase recruitment domain (CARD)
containing molecules. Several molecules including caspases
and adaptor FADD contain DEDs. A novel protein that
interacts with DED of caspase-8 and –10, and FADD was
identified recently and designated DEDAF for DED
associated factor (1). DEDAF is identical to the
transcriptional repressor RYBP (2). DEDAF/RYBP is
expressed in multiple tissues and cell lines. DEDAF interacts
with FADD and augments the formation of
CD95/FADD/capase-8 complexes at the cell membrane, and
interacts with DED-containing DNA biding protein (DEDD) in
the nucleus indicating it is involved in the regulation of both
cytoplasmic and nuclear events of apoptosis.
SOURCE:
Rabbit anti-DEDAF polyclonal antibody was raised against a
synthetic peptide (TPKGDMSAVNDESF) corresponding to
amino acids 215 to 228 of human DEDAF (1,2). The
sequence is identical to that of mouse origin (2).
APPLICATION:
This antibody can be used for detection of DEDAF by
Western blot at 0.5 to 1 µg/ml. Human A549 or HepG2 cell
lysate can be used as a positive control. A band at
approximately 32 kDa can be detected. It is human, mouse,
and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of DEDAF
expression in human A549
(lane A), HepG2 (lane B), and
mouse 3T3 (lane C) cell lysates
with anti-DEDAF at 1 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2227P).
Human HepG2 cell lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1211).
REFERENCES:
1. Zheng L, Schickling O, Peter ME, Lenardo MJ. The death
effector domain-associated factor (DEDAF) plays distinct
regulatory roles in the nucleus and cytoplasm. J Biol Chem.
2001;276(34):31945-52.
2. Garcia E, Marcos-Gutierrez C, del Mar Lorente M, Moreno JC,
Vidal M. RYBP, a new repressor protein that interacts with
components of the mammalian Polycomb complex, and with the
transcription factor YY1. EMBO J. 1999;18(12):3404-18.
(RD0201)

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Anti-Survivin (NT) TIAP/API4
CATALOG No.: 2233
BACKGROUND:
Apoptosis, or programmed cell death, is related to many
diseases, such as cancer. Apoptosis is triggered by a variety
of stimuli including members in the TNF family and
prevented by the inhibitor of apoptosis (IAP) proteins. IAP
proteins form a conserved gene family that binds to and
inhibits cell death proteases. A novel IAP protein was
recently identified and designated survivin, apoptosis
inhibitor 4 (API4), and TIAP (1-3). Survivin/TIAP interacted
with the processed form of caspase-3 and inhibited its
proteolytic activity. Survivin/TIAP is predominantly expressed
in tissues of embryos, transformed cell lines, and many
human cancers and lymphomas (1).
SOURCE:
Rabbit anti-survivin (NT) polyclonal antibody was raised
against a peptide corresponding to amino acids 1 to 12 of
human origin (1).
APPLICATION:
This polyclonal antibody can be used for detection of survivin
by Western blot at 0.5 to 1 µg/ml. MOLT4 cell lysate can be
used as positive control and an approximate 17 kDa band
should be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2233P). MOLT4 cell
lysate, 200 µg at 2 mg/ml, is available for positive control
(Catalog No. 1206).
Western blot analysis of
survivin in MOLT4 cell
lysate in the absence (A) or
presence (B) of blocking
peptide with anti-survivin
(NT) at 1 µg/ml.
REFERENCES:
1. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene,
survivin, expressed in cancer and lymphoma. Nat Med 1997;3:917-
21
2. Li F, Ambrosini G, Chu EY, Plescia J, Tognin S, Marchisio PC,
Altieri DC. Control of apoptosis and mitotic spindle checkpoint by
survivin. Nature 1998;396:580-4
3. Kobayashi K, Hatano M, Otaki M, Ogasawara T, Tokuhisa T.
Expression of a murine homologue of the inhibitor of apoptosis
protein is related to cell proliferation. Proc Natl Acad Sci USA
1999;96:1457-62
(WD0600)

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Anti-Survivin (CT) TIAP/API4
CATALOG No.: 2235
BACKGROUND:
Apoptosis, or programmed cell death, is related to many
diseases, such as cancer. Apoptosis is triggered by a variety
of stimuli including members in the TNF family and
prevented by the inhibitor of apoptosis (IAP) proteins. IAP
proteins form a conserved gene family that binds to and
inhibits cell death proteases. A novel IAP protein was
recently identified and designated survivin, apoptosis
inhibitor 4 (API4), and TIAP (1-3). Survivin/TIAP interacted
with the processed form of caspase-3 and inhibited its
proteolytic activity. Survivin/TIAP is predominantly expressed
in tissues of embryos, transformed cell lines, and many
human cancers and lymphomas (1,3).
SOURCE:
Rabbit anti-survivin (CT) polyclonal antibody was raised
against a peptide corresponding to amino acids 129 to 142
of human origin (1).
APPLICATION:
This polyclonal antibody can be used for detection of survivin
by Western blot at 0.5 to 1 µg/ml. MOLT4 cell lysate can be
used as positive control and an approximate 17 kDa band
should be detected. For research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2235P). MOLT4 cell
lysate, 200 µg at 2 mg/ml, is available for positive control
(Catalog No. 1206).
Western blot analysis of
survivin in MOLT4 cell
lysate in the absence (A)
or presence (B) of
blocking peptide with
anti-survivin (CT) at 1
µg/ml.
REFERENCES:
1. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene,
survivin, expressed in cancer and lymphoma. Nat Med 1997;3:917-
21
2. Li F, Ambrosini G, Chu EY, Plescia J, Tognin S, Marchisio PC,
Altieri DC. Control of apoptosis and mitotic spindle checkpoint by
survivin. Nature 1998;396:580-4
3. Kobayashi K, Hatano M, Otaki M, Ogasawara T, Tokuhisa T.
Expression of a murine homologue of the inhibitor of apoptosis
protein is related to cell proliferation. Proc Natl Acad Sci USA
1999;96:1457-62
(WD0600)

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Anti-Survivin (CT) TIAP/API4
CATALOG No.: 2237
BACKGROUND:
Apoptosis, or programmed cell death, is related to many
diseases, such as cancer. Apoptosis is triggered by a variety
of stimuli including members in the TNF family and
prevented by the inhibitor of apoptosis (IAP) proteins. IAP
proteins form a conserved gene family that binds to and
inhibits cell death proteases. A novel IAP protein was
recently identified and designated survivin, apoptosis
inhibitor 4 (API4), and TIAP (1-3). Survivin/TIAP interacted
with the processed form of caspase-3 and inhibited its
proteolytic activity. Survivin/TIAP is predominantly expressed
in tissues of embryos, transformed cell lines, and many
human cancers and lymphomas (1,3).
SOURCE:
Rabbit anti-survivin (CT) polyclonal antibody was raised
against a synthetic peptide (AKTTRQSIEQLAA)
corresponding to amino acids 128 to 140 of mouse origin (3).
APPLICATION:
This polyclonal antibody can be used for detection of survivin
by Western blot at 0.5 to 1 µg/ml. Mouse spleen tissue lysate
can be used as positive control and an approximate 17 kDa
band can be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2237P). Mouse spleen
lysate, 200 µg at 2 mg/ml, is available for positive control
(Catalog No. 1406).
Western blot analysis of
survivin in mouse spleen
tissue lysate with anti-survivin
(CT) at 1 µg/ml.
REFERENCES:
1. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene,
survivin, expressed in cancer and lymphoma. Nat Med 1997;3:917-
21
2. Li F, Ambrosini G, Chu EY, Plescia J, Tognin S, Marchisio PC,
Altieri DC. Control of apoptosis and mitotic spindle checkpoint by
survivin. Nature 1998;396:580-4
3. Kobayashi K, Hatano M, Otaki M, Ogasawara T, Tokuhisa T.
Expression of a murine homologue of the inhibitor of apoptosis
protein is related to cell proliferation. Proc Natl Acad Sci USA
1999;96:1457-62
(WD1000)

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Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-AIF (NT)
CATALOG No.: 2239
BACKGROUND:
Apoptosis is characterized by several morphological nuclear
changes including chromatin condensation and nuclear
fragmentation. These changes are triggered by the activation
of members of caspase family, caspase activated DNase,
and several novel proteins (1). A novel gene, the product of
which causes chromatin condensation and DNA
fragmentation, was recently identified, cloned, and
designated apoptosis inducing factor (AIF) (2). Like the
critical molecules, cytochrome c and caspase-9, in
apoptosis, AIF localizes in mitochondria. AIF translocates to
the nucleus when apoptosis is induced and induces
mitochondria to release the apoptogenic proteins
cytochrome c and caspase-9. AIF induces chromatin
condensation and DNA fragmentation, which are the
hallmarks of apoptosis, of the isolated nucleus and the
nucleus in live cells by microinjection. AIF is highly
conserved between human and mouse and widely
expressed (2).
SOURCE:
Rabbit anti-AIF (N-terminus of mature AIF) polyclonal
antibody was raised against a peptide corresponding to
amino acids 109 to 122 of human AIF (2).
APPLICATION:
This polyclonal antibody can be used for detection of AIF by
Western blot at 0.25 to 1 µg/ml. K562 cell lysate can be used
as positive control and a 67 kDa band should be detected.
For research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of
AIF in K562 cell lysate with
anti-AIF (NT) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2239P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death. Nature
1999;401:127-8
2. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular
characterization of mitochondrial apoptosis-inducing factor. Nature
1999;397:441-6
(WD0500)

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Anti-Acinus (NP)
CATALOG No.: 2241
BACKGROUND:
Chromatin condensation and nuclear fragmentation (CCNF)
is the hallmark of apoptosis. CCNF is triggered by the
activation of members of caspase family, caspase activated
DNase (CAD/DFF40), and several novel proteins including
AIF and CIDE (1). A new inducer of chromatin condensation
was recently identified and designated Acinus (for apoptotic
chromatin condensation inducer in the nucleus). Acinus is
cleaved by caspase-3 and an additional unknown protease
generating a small active peptide p17, which causes
chromatin condensation in vitro when it is added to purified
nuclei. Acinus also induces apoptotic chromatin
condensation in cells. Acinus is ubiquitously expressed.
Three different spliced forms of Acinus have been identified
in human and mouse and designated AcinusL, AcinusS and
AcinusS’ (2).
SOURCE:
Rabbit anti-Acinus (NP) polyclonal antibody was raised
against a peptide (DDPVRTAQVPSPPRGK) corresponding
to amino acids 994 to 1009 of human AcinusL, 267 to 282 of
human AcinusS’, or 236 to 251 of human AcinusS, which are
identical to those of mouse Acinus (2). The selected
antigenic sequence is located near the N-terminus of active
peptide p17.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
Acinus in K562 whole cell
lysate with anti-Acinus (NP)
at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2241P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death.
Nature 1999 ;401:127-8.
2. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto
Y. Acinus is a caspase-3-activated protein required for apoptotic
chromatin condensation. Nature 1999 401:168-73.
(WD0800)
APPLICATION:
This polyclonal antibody can be used for detection of Acinus
by Western blot at 0.5 to 1 µg/ml. K562 cell lysate can be
used as positive control and an approximate 220 kDa band
can be detected. For research use only.

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Anti-Caspase-13 / ERICE
CATALOG No.: 2245
BACKGROUND:
Apoptosis is related to many diseases and induced by a
family of cell death receptors and their ligands. Cell death is
finally caused by members of the caspase family of
proteases and caspase activated DNases. A novel member
in the caspase family was recently identified and designated
ERICE (for Evolutionarily Related Interleukin-1 β Converting
Enzyme) and caspase-13 (1). Caspase-13 belongs to the
ICE subfamily of caspases. Overexpression of caspase-13
induces apoptosis. Caspase-13 was activated by caspase-8,
which is a key enzyme in death receptor induced apoptosis.
Caspase-13 is expressed in a variety of human tissues and
cell lines (1).
SOURCE:
Rabbit anti-caspase-13 polyclonal antibody was raised
against a peptide corresponding to amino acids 91 to 105 of
human Acaspase-13 (1).
APPLICATION:
This polyclonal antibody can be used for detection of AIF by
Western blot at 0.5 to 1 µg/ml. HL60 cell lysate can be used
as positive control and a 43 kDa band should be detected. It
is human, mouse and rat reactive. For research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2245P). HL60 cell lysate,
200 µg at 2 mg/ml, is available for positive control (Catalog
No. 1209).
Western blot analysis of casp-
13 in human HL60 cell lysate
(A), mouse brain (B) and rat
brain (C) tissue lysates with
anti-casp-13 at 1 µg/ml.
REFERENCES:
1. Humke EW, Ni J, Dixit VM. ERICE, a novel FLICE-activatable
caspase. J Biol Chem 1998;273:15702-7
(WD0500)

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Anti-BACE2 / Asp1 (NT)
CATALOG No.: 2247
BACKGROUND:
Accumulation of the amyloid-β (Aβ) plaque in the cerebral
cortex is a critical event in the pathogenesis of Alzheimer’s
disease. Aβ peptide is generated by proteolytic cleavage of
the β−amyloid protein precursor (APP) at β- and γ-sites by
proteases. The long-sought β−secretase was recently
identified by several groups independently and designated
beta-site APP cleaving enzyme (BACE) and aspartyl
protease 2 (Asp2) (1-4). A BACE homolog was recently
cloned and designated BACE2, Asp1, DRAP (for Down
region aspartic protease), and memapsin 1 (4-9). BACE2
also cleaves APP at β-site and at a different site within Aβ
(8). BACE2 locates on chromosome 21q22.3, the so-called
‘Down critical region’, suggesting that BACE2 and Aβ may
also contribute to the pathogenesis of Down syndrome (6,7)
SOURCE:
This rabbit polyclonal antibody was raised against a
synthetic peptide (APTPGPGTPAERHADG) corresponding
to amino acids 44 to 59 of human BACE2 (4).
APPLICATION:
This antibody can be used for detection of BACE2 by
Western blot at 0.5 to 1 µg/ml. Human heart tissue lysate
can be used as positive control. It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year. Azide free antibody is
available.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2247P).
Human heart tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1301).
Western blot analysis of
BACE2 in human (A) and
mouse (B) heart tissue
lysates with anti-BACE2
(CT) at 1 µg/ml.
REFERENCES:
1. Vassar R, et al. Beta-secretase cleavage of Alzheimer's amyloid
precursor protein by the transmembrane aspartic protease BACE.
Science 1999;286:735-41
2. Hussain I, et al. Identification of a novel aspartic protease (Asp
2) as beta-secretase. Mol Cell Neurosci 1999;14:419-27
3. Sinha S, et al. Purification and cloning of amyloid precursor
protein beta-secretase from human brain. Nature 1999;402:537-40
4. Yan R, et al. Membrane-anchored aspartyl protease with
Alzheimer's disease beta-secretase activity. Nature 1999;402:533-
7
5. Lin X, et al. Human aspartic protease memapsin 2 cleaves the
beta-secretase site of beta-amyloid precursor protein. Proc Natl
Acad Sci USA 2000 15;97:1456-60
6. Acquati F, et al. The gene encoding DRAP (BACE2), a
glycosylated transmembrane protein of the aspartic protease
family, maps to the down critical region. FEBS Lett 2000;468:59-64
7. Solans A, et al. A new aspartyl protease on 21q22.3, BACE2, is
highly similar to Alzheimer's amyloid precursor protein betasecretase.
Cytogenet Cell Genet 2000;89:177-184
8. Farzan M, et al. BACE2, a beta -secretase homolog, cleaves at
the beta site and within the amyloid-beta region of the amyloid-beta
precursor protein. Proc Natl Acad Sci USA 2000;97:9712-7
9. Bennett BD, et al. Expression analysis of BACE2 in brain and
peripheral tissues. J Biol Chem 2000;275:20647-51
(WD0900)

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Anti-BACE2 / Asp1 (CT)
CATALOG No.: 2249
BACKGROUND:
Accumulation of the amyloid-β (Aβ) plaque in the cerebral
cortex is a critical event in the pathogenesis of Alzheimer’s
disease. Aβ peptide is generated by proteolytic cleavage of
the β−amyloid protein precursor (APP) at β- and γ-sites by
proteases. The long-sought β−secretase was recently
identified by several groups independently and designated
beta-site APP cleaving enzyme (BACE) and aspartyl
protease 2 (Asp2) (1-4). BACE/Asp2 is a novel
transmembrane aspartic protease and co-localizes with
APP. A BACE homolog was recently cloned and designated
BACE2, Asp1, DRAP (for Down region aspartic protease),
and memapsin 1 (4-9). BACE2 also cleaves APP at β-site
and at a different site within Aβ (8). BACE2 locates on
chromosome 21q22.3, the so-called ‘Down critical region’,
suggesting that BACE2 and Aβ may also contribute to the
pathogenesis of Down syndrome (6,7)
SOURCE:
This rabbit polyclonal antibody was raised against a peptide
corresponding to amino acids 496 to 511 of human BACE2
(4).
APPLICATION:
This antibody can be used for detection of BACE2 by
Western blot at 0.5 to 1 µg/ml. Human heart tissue lysate
can be used as positive control. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year. Azide free antibody is
available.
RELATED PRODUCTS:
Western blot analysis of
BACE2 in human heart
tissue lysate in the absence
(A) or presence (B) of
blocking peptide (2249P)
with anti-BACE2 (CT) at 1
µg/ml.
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2249P).
Human heart tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1301).
REFERENCES:
1. Vassar R, et al. Beta-secretase cleavage of Alzheimer's amyloid
precursor protein by the transmembrane aspartic protease BACE.
Science 1999;286:735-41
2. Hussain I, et al. Identification of a novel aspartic protease (Asp
2) as beta-secretase. Mol Cell Neurosci 1999;14:419-27
3. Sinha S, et al. Purification and cloning of amyloid precursor
protein beta-secretase from human brain. Nature 1999;402:537-40
4. Yan R, et al. Membrane-anchored aspartyl protease with
Alzheimer's disease beta-secretase activity. Nature 1999;402:533-
7
5. Lin X, et al. Human aspartic protease memapsin 2 cleaves the
beta-secretase site of beta-amyloid precursor protein. Proc Natl
Acad Sci USA 2000 15;97:1456-60
6. Acquati F, et al. The gene encoding DRAP (BACE2), a
glycosylated transmembrane protein of the aspartic protease
family, maps to the down critical region. FEBS Lett 2000;468:59-64
7. Solans A, et al. A new aspartyl protease on 21q22.3, BACE2, is
highly similar to Alzheimer's amyloid precursor protein betasecretase.
Cytogenet Cell Genet 2000;89:177-184
8. Farzan M, et al. BACE2, a beta-secretase homolog, cleaves at
the beta site and within the amyloid-beta region of the amyloid-beta
precursor protein. Proc Natl Acad Sci USA 2000;97:9712-7
9. Bennett BD, et al. Expression analysis of BACE2 in brain and
peripheral tissues. J Biol Chem 2000;275:20647-51
(WD0900)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-BACE / Asp2 (CT)
CATALOG No.: 2253
BACKGROUND:
Accumulation of the amyloid-β (Aβ) plaque in the cerebral
cortex is a critical event in the pathogenesis of Alzheimer’s
disease. Aβ peptide is generated by proteolytic cleavage of
the β−amyloid protein precursor (APP) at β- and γ-sites by
two proteases. APP is first cleaved by β−secretase,
producing a soluble derivative of the protein and a
membrane anchored 99-amino acid carboxy-terminal
fragment (C99). The C99 fragment serves as substrate for
γ−secretase to generate the 4 kDa amyloid-β peptide, which
is deposited in the brains of all suffers of Alzheimer’s
disease. The long-sought β−secretase was recently
identified by several groups independently and designated
beta-site APP cleaving enzyme (BACE) and aspartyl
protease 2 (Asp2) (1-4). BACE/Asp2 is a novel
transmembrane aspartic protease and colocalizes with APP.
SOURCE:
This rabbit polyclonal antibody was raised against a peptide
corresponding to amino acids 485 to 501 of human BACE
(1). The peptide sequence differs from those of mouse and
rat BACE by one amino acid (1).
APPLICATION:
This antibody can be used for detection of BACE by Western
blot at 0.5 to 1 µg/ml. Human brain tissue lysate can be used
as positive control and an approximately 70 kDa band
should be detected. It is human and mouse reactive. For
research use only.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year. Azide free antibody is
available.
Western blot analysis of
BACE in human brain tissue
lysate in the absence (A) or
presence (B) of blocking
peptide (2253P) and in mouse
3T3 cell lysate (C) with anti-
BACE (CT) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2253P).
Human brain tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1303).
REFERENCES:
1. Vassar R, Bennett BD, Babu-Khan S, et al. Beta-secretase
cleavage of Alzheimer's amyloid precursor protein by the
transmembrane aspartic protease BACE. Science 1999;286:735-
41
2. Hussain I, Powell D, Howlett DR, et al. Identification of a novel
aspartic protease (Asp 2) as beta-secretase. Mol Cell Neurosci
1999;14:419-27
3. Yan R, Bienkowski MJ, Shuck ME, et al. Membrane-anchored
aspartyl protease with Alzheimer's disease beta-secretase activity.
Nature 1999;402:533-7
4. Sinha S, Anderson JP, Barbour R, et al. Purification and cloning
of amyloid precursor protein beta-secretase from human brain.
Nature 1999;402:537-40 (WD0500)

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Anti-AIF (IN)
CATALOG No.: 2267
BACKGROUND:
Apoptosis is characterized by several morphological nuclear
changes including chromatin condensation and nuclear
fragmentation. These changes are triggered by the activation
of members of caspase family, caspase activated DNase,
and several novel proteins (1). A novel gene, the product of
which causes chromatin condensation and DNA
fragmentation, was recently identified, cloned, and
designated apoptosis inducing factor (AIF) (2). Like the
critical molecules, cytochrome c and caspase-9, in
apoptosis, AIF localizes in mitochondria. AIF translocates to
the nucleus when apoptosis is induced and induces
mitochondria to release the apoptogenic proteins
cytochrome c and caspase-9. AIF induces chromatin
condensation and large scale DNA fragmentation, which are
the hallmarks of apoptosis, of the isolated nucleus and the
nucleus in live cells by microinjection and apoptosis stimuli
(2,3). AIF is highly conserved between human and mouse
and widely expressed (2).
SOURCE:
Rabbit anti-AIF (IN) polyclonal antibody was raised against a
peptide corresponding to amino acids 517 to 531 of human
AIF (2). This sequence is identical to those of mouse and rat
AIF (2).
Western blot analysis of AIF
in K562 cell lysate (A), rat
heart (B), and mouse heart
(C) tissue lysates with anti-
AIF (IN) at 1 µg/ml.
STORAGE:
It is supplied as ion exchange chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2267P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death. Nature
1999;401:127-8
2. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular
characterization of mitochondrial apoptosis-inducing factor. Nature
1999;397:441-6
APPLICATION:
This polyclonal antibody can be used for detection of AIF by
Western blot at 0.25 to 1 µg/ml. K562 cell lysate can be used
as positive control and a 67 kDa band should be detected. It
is human, mouse and rat reactive. For research use only.
3. Daugas E, Susin SA, Zamzami N, et al. Mitochondrio-nuclear
translocation of AIF in apoptosis and necrosis. FASEB J
2000;14:729-39
(WD0500)

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Anti-FLASH (CT)
CATALOG No.: 2271
BACKGROUND:
A novel mammalian CED-4 homologous was recently
identified and cloned in mouse (1) and human (2) and
designated FLASH (for FLICE-associated huge protein).
FLASH is involved in Fas induced apoptosis. It is recruited to
Fas after the receptor cross-linking. Overexpression of wild
type of FLASH facilitates and its dominant negative form
inhibits Fas induced apoptosis. FLASH interacts with the
DEDs of caspase-8 and FADD through the DED-like domain
of FLASH and mediates activation of caspase-8 (1). There
are parallels between FLASH and Apaf-1/CED-4 although
there are arguments against their structural similarity (1,2).
FLASH is widely expressed.
SOURCE:
Rabbit anti-FLASH (CT) polyclonal antibody was raised
against a synthetic peptide (SERFQQLMKLFEKSKC)
corresponding to amino acids 1253 to 1268 of human origin,
which differ from those of mouse by one amino acid (1,2).
APPLICATION:
This polyclonal antibody can be used for detection of FLASH
by Western blot at 0.25 to 0.5 µg/ml. HeLa cell lysate can be
used as positive control and an approximate 220 kDa band
can be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
FLASH in HeLa whole cell
lysate with anti-FLASH (CT)
at 0.5 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2271P).
HeLa cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1201).
REFERENCES:
1. Imai Y, Kimura T, Murakami A, Yajima N, Sakamaki K,
Yonehara S. The CED-4-homologous protein FLASH is involved in
Fas-mediated activation of caspase-8 during apoptosis. Nature
1999;398:777-85
2. Koonin EV, Aravind L, Hofmann K, Tschopp J, Dixit VM
Apoptosis. Searching for FLASH domains. Nature 1999;401:662-3
3. Medema JP. Apoptosis. Life and death in a FLASH. Nature
1999;398:756-7
(WD0800)

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Anti-F1Aα
CATALOG No.: 2279
BACKGROUND:
Fas and tumor necrosis factor receptor 1 (TNFR1) are two
prototype members in the death receptor family. A novel
protein that associates with the intracellular domains of Fas
and TNFR1 was recently identified and designated
F1Aα and FEM1β (1,2). F1Aα/FEM1β is the homologue of C.
elegans sex determining protein FEM-1 (1,2). FEM-
1/F1Aα is cleaved by CED-3 and caspase (3). FEM-
1/F1Aα associates with CED-4 and its mammalian
homologue Apaf-1 (3). Overexpression of F1Aα induces
apoptosis. F1Aα is therefore a novel member of the death
receptor associated protein that mediates apoptosis. F1Aα
is expressed in a variety of human and mouse tissues (1,2)
SOURCE:
Rabbit anti-F1Aα polyclonal antibody was raised against a
peptide (DINYQDQIPRTLEE) corresponding to amino acids
609 to 622 of human F1Aα (1). This sequence is identical to
the corresponding sequence of mouse FEM1β (2).
APPLICATION:
This polyclonal antibody can be used for detection of F1Aα
by Western blot at 0.5 to 1 µg/ml. Mouse liver tissue lysate
can be used as positive control and an approximately 70 kDa
band can be detected. It is human, mouse, and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2279P).
Mouse liver tissue lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1404).
Western blot analysis of F1Aα
in mouse (A) and rat (B) liver
tissue lysates with anti- F1Aα
at 1 µg /ml.
REFERENCES:
1. Chan SL, Tan KO, Zhang L, Yee KS, Ronca F, Chan MY, Yu
VC. F1Aalpha, a death receptor-binding protein homologous to the
Caenorhabditis elegans sex-determining protein, FEM-1, is a
caspase substrate that mediates apoptosis. J Biol Chem.
1999;274(45):32461-8.
2. Ventura-Holman T, Maher JF. Sequence, organization, and
expression of the human FEM1B gene. Biochem Biophys Res
Commun 2000;267(1):317-20
3. Chan SL, Yee KS, Tan KM, Yu VC. The Caenorhabditis elegans
sex determination protein FEM-1 is a CED-3 substrate that
associates with CED-4 and mediates apoptosis in mammalian
cells. J Biol Chem. 2000;275(24):17925-8.
(WD0102)

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Anti-RIP3
CATALOG No.: 2283
BACKGROUND:
Certain serine/threonine protein kinases, such as ASK1, RIP,
DAP, and ZIP kinases, are mediators of apoptosis. Receptor
interacting proteins including RIP and RIP2/RICK mediate
apoptosis induced by TNFR1 and Fas, two prototype
members in the death receptor family. A novel member in
the RIP kinase family was recently identified and designated
RIP3 (1-3). RIP3 contains N-terminal kinase domain but,
unlike RIP or RIP2, lacks the C-terminal death or CARD
domain. RIP3 binds to RIP and TNFR1, mediates TNFR1
induced apoptosis, and attenuates RIP and TNFR1 induced
NF-κB activation. Overexpression of RIP3 induces apoptosis
and NF-κB activation. The messenger RNA of RIP3 is
expressed in a subset of adult tissues (2,3).
SOURCE:
Rabbit anti-RIP3 polyclonal antibody was raised against a
peptide (AQFGRGRGWQPFHK) corresponding to amino
acids 473 to 486 of murine RIP3 (3).
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2383P).
Mouse 3T3 whole cell lysate, 200 µg at 2 mg/ml, is
available for positive control (Catalog No. 1212).
Western blot analysis of RIP3 in
mouse 3T3 whole cell lysate in
the absence (A) or presence (B)
of blocking peptide with anti-
RIP3 at 1 µg /ml.
REFERENCES:
1. Yu PW, Huang BC, Shen M, Quast J, Chan E, Xu X, Nolan GP,
Payan DG, Luo Y. Identification of RIP3, a RIP-like kinase that
activates apoptosis and NFkappaB. Curr Biol. 1999;9(10):539-42.
2. Sun X, Lee J, Navas T, Baldwin DT, Stewart TA, Dixit VM. RIP3,
a novel apoptosis-inducing kinase. J Biol Chem.
1999;274(24):16871-5.
APPLICATION:
This polyclonal antibody can be used for detection of RIP3
by Western blot at 0.5 to 1 µg/ml. 3T3 cell lysate can be
used as positive control and an approximately 57 kDa band
can be detected. It is mouse and rat reactive. For research
use only.
3. Pazdernik NJ, Donner DB, Goebl MG, Harrington MA. Mouse
receptor interacting protein 3 does not contain a caspase-recruiting
or a death domain but induces apoptosis and activates NFkappaB.
Mol Cell Bio. 1999; 19(10):6500-8
(WD0102)
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.

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Anti-ASC / TMS1
CATALOG No.: 2287
BACKGROUND:
Apoptosis is regulated by death domain (DD) and/or caspase
recruitment domain (CARD) containing molecules and a
caspase family of proteases. CARD containing cell death
regulators include RAIDD, RICK, BCL10, Apaf-1, ARC,
caspase-9, and caspase-2. A novel CARD domain
containing protein was recently identified in human and
mouse and designated ASC and TMS1 (1-3). Ectopic
expression of ASC/TMS1 induced apoptosis through
activation of caspase-9 and inhibited the survival of human
breast cancer cells (3,4). Overexpression of ASC/TMS1
induced DNA fragmentation (4). ASC/TMS1 is expressed in
a variety of human and mouse tissues (1, 2)
SOURCE:
Rabbit anti-ASC/TMS1 polyclonal antibody was raised
against a synthetic peptide (RESQSYLVEDLERS)
corresponding to amino acids 182 to 195 of human ASC (1).
APPLICATION:
This polyclonal antibody can be used for detection of
ASC/TMS1 by Western blot at 1 µg/ml. HL60 whole cell
lysate can be used as positive control and an approximately
25 kDa band can be detected. It is human reactive. For
research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2287P). HL60 whole cell
lysate, 200 µg at 2 mg/ml, is available for positive control
(Catalog No. 1209).
Western blot analysis of ASC in
HL60 whole cell lysate in the
absence (A) or presence (B) of
blocking peptide (2287P) with anti-
ASC at 1 µg /ml.
REFERENCES:
1. Masumoto J, Taniguchi S, Ayukawa K, Sarvotham H, Kishino T,
Niikawa N, Hidaka E, Katsuyama T, Higuchi T, Sagara J. ASC, a
novel 22-kDa protein, aggregates during apoptosis of human
promyelocytic leukemia HL-60 cells. J Biol Chem.
1999;274(48):33835-8.
2. Masumoto J, Taniguchi S, Nakayama K, Ayukawa K, Sagara J.
Murine Ortholog of ASC, a CARD-Containing Protein, Self-
Associates and Exhibits Restricted Distribution in Developing
Mouse Embryos. Exp Cell Res. 2001;262(2):128-133.
3. Conway KE, McConnell BB, Bowring CE, Donald CD, Warren
ST, Vertino PM. TMS1, a novel proapoptotic caspase recruitment
domain protein, is a target of methylation-induced gene silencing in
human breast cancers. Cancer Res. 2000;60(22):6236-42.
4. McConnell BB, Vertino PM. Activation of a caspase-9-mediated
apoptotic pathway by subcellular redistribution of the novel
caspase recruitment domain protein TMS1. Cancer Res.
2000;60(22):6243-7.
(WD0102)

13100 Kirkham Way
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Anti-Bnip3L (IN) Bnip3α, Nix
CATALOG No.: 2289
BACKGROUND:
Members in the Bcl-2 family are critical regulators of
apoptosis by either inhibiting or promoting cell death. Bcl-2
homology 3 (BH3) domain is a potent death domain. BH3
domain containing pro-apoptotic proteins, including Bad,
Bax, Bid, Bik, Hrk, Nip3, and Bim, form a growing subclass
of the Bcl-2 family. A novel BH3 domain containing protein
was recently identified and designated Bnip3L, Bnip3α, and
Nix (for Nip3-like protein X) (1-3). Bnip3L/Bnip3α/Nix is a
homolog of the E1B 19K/Bcl-2 binding and pro-apoptotic
protein Bnip3. Overexpression of Bnip3L induces apoptosis
(2,3). Bnip3L interacts with and overcomes suppresses by
Bcl-2 and Bcl-xL. Bnip3L is localized in mitochondria. The
messenger RNA of Bnip3L is ubiquitously expressed in
human tissues (1,2). Bnip3L and Bnip3 form a new subfamily
of the pro-apoptotic mitochondrial proteins.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of Bnip3L
in K562 whole cell lysate in the
absence (A), or presence (B) of
immunogenic peptide (2289P)
with anti-Bnip3L (IN) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2289P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
SOURCE:
Rabbit anti-Bnip3L (IN) polyclonal antibody was raised
against a peptide (DAQHESGQSSSRGSSH) corresponding
to amino acids 77 to 92 of human origin, which are identical
to those of mouse Bnip3L (3).
APPLICATION:
This polyclonal antibody can be used for detection of Bnip3L
by Western blot at 0.5 to 1 µg/ml. K562 cell lysate can be
used as positive control and the approximate 40 kDa top
band represents monomer of Bnip3L (4). It is human and
mouse reactive. For research use only.
REFERENCES:
1. Matsushima M, Fujiwara T, Takahashi E, et al. Isolation,
mapping, and functional analysis of a novel human cDNA (BNIP3L)
encoding a protein homologous to human NIP3. Genes
Chromosomes Cancer 1998;21:230-5
2. Yasuda M, Han JW, Dionne CA, Boyd JM, Chinnadurai G.
BNIP3alpha: a human homolog of mitochondrial proapoptotic
protein BNIP3. Cancer Res 1999;59:533-7
3. Chen G, Cizeau J, Vande Velde C, et al. Nix and Nip3 form a
subfamily of pro-apoptotic mitochondrial proteins. J Biol Chem
1999;274(1):7-10
4. Imazu T, Shimizu S, Tagami S, et al. Bcl-2/E1B 19 kDainteracting
protein 3-like protein (Bnip3L) interacts with bcl-2/Bcl-xL
and induces apoptosis by altering mitochondrial membrane
permeability. Oncogene. 1999;18:4523-9 (RD1200)

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Anti-DcR1 (ED2) TRAIL-R3, TRID, LIT
CATALOG No.: 2299
BACKGROUND:
Apoptosis is induced by certain cytokines including TNF and
Fas ligand in the TNF family through their death domain
containing receptors. TRAIL/Apo2L is a new member of the
TNF family and induces apoptosis of a variety of tumor cell
lines. DR4 and DR5 are the recently identified functional
receptors for TRAIL (1-3). Two decoy receptors for TRAIL
have been identified and designated DcR1/TRID/TRAIL-
R3/LIT (2-7) and DcR2/TRAIL-R4/TRUNDD (8-10). DcR1
has extracellular TRAIL-binding domain but lacks
intracellular signaling domain. It is a glycophospholipidanchored
cell surface protein. DcR1 transcripts are
expressed in many normal human tissues but not in most
cancer cell lines (2,3). Overexpression of DcR1 did not
induce apoptosis, but attenuated TRAIL-induced apoptosis
(2,3).
SOURCE:
Rabbit anti-DcR1 (ED2) polyclonal antibody was raised
against a peptide (CKEGTFRNENSPE) corresponding to
amino acids 111 to 123 at extracellular domain of human
DcR1 precursor (2-3).
APPLICATION:
This polyclonal antibody can be used for detection of DcR1
by Western blot at 0.5 to 1 µg/ml. HeLa cell lysate can be
used as positive control and an approximate 65 kDa band
can be detected (6). It is human, mouse, and rat reactive.
For research use only.
STORAGE:
It is supplied as chromatography purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at -20°C.
Stable for one year at 2-8°C.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2299P).
HeLa cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1201).
Western blot analysis of DcR1 in
HeLa cell (A), mouse (B) and rat (C)
liver tissue lysates with anti-DcR1
(ED2) at 1 µg/ml.
REFERENCES:
1. Pan G; O'Rourke K; Chinnaiyan et al.. The receptor for the cytotoxic
ligand TRAIL. Science; 1997;276:111-113
2. Pan G, Ni J, Wei YF, et al. An antagonist decoy receptor and a death
domain-containing receptor for TRAIL. Science 1997;277:815-8
3. Sheridan JP, Marsters SA, Pitti RM, et al. A. Control of TRAIL-induced
apoptosis by a family of signaling and decoy receptors. Science
1997;277:818-21
4. Degli-Esposti MA, Smolak PJ, Walczak H, et al, Smith CA. Cloning and
characterization of TRAIL-R3, a novel member of the emerging TRAIL
receptor family. J Exp Med 1997;186(7):1165-70
5. MacFarlane M, Ahmad M, Srinivasula SM, et al. Identification and
molecular cloning of two novel receptors for the cytotoxic ligand TRAIL. J
Biol Chem 1997;272(41):25417-20
6. Schneider P, Bodmer JL, Thome M, Hofmann K, Holler N, Tschopp J.
Characterization of two receptors for TRAIL. FEBS Lett 1997;416(3):329-34
7. Mongkolsapaya J, Cowper AE, Xu XN, et al. Lymphocyte inhibitor of
TRAIL (TNF-related apoptosis -inducing ligand): a new receptor protecting
lymphocytes from the death ligand TRAIL. J Immunol 1998;160(1):3-6
8. Marsters SA, Sheridan JP, Pitti RM, et al. A novel receptor for
Apo2L/TRAIL contains a truncated death domain. Curr Biol 1997;7:1003-6
9. Degli-Esposti MA, Dougall WC, Smolak PJ, et al. The novel receptor
TRAIL-R4 induces NF-kappaB and protects against TRAIL-mediated
apoptosis, yet retains an incomplete death domain. Immunity 1997;7:813-20
10. Pan G, Ni J, Yu G, et al. TRUNDD, a new member of the TRAIL
receptor family that antagonizes TRAIL signalling. FEBS Lett 1998;424:41-5
(WD0800)

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Anti-AIF (CT)
CATALOG No.: 2301
BACKGROUND:
Apoptosis is characterized by several morphological nuclear
changes including chromatin condensation and nuclear
fragmentation. These changes are triggered by the activation
of members of caspase family, caspase activated DNase,
and several novel proteins (1). A novel gene, the product of
which causes chromatin condensation and DNA
fragmentation, was recently identified, cloned, and
designated apoptosis inducing factor (AIF) (2). Like the
critical molecules, cytochrome c and caspase-9, in
apoptosis, AIF localizes in mitochondria. AIF translocates to
the nucleus when apoptosis is induced and induces
mitochondria to release the apoptogenic proteins
cytochrome c and caspase-9. AIF induces chromatin
condensation and DNA fragmentation, which are the
hallmarks of apoptosis, of the isolated nucleus and the
nucleus in live cells by microinjection. AIF is highly
conserved between human and mouse and widely
expressed (2).
SOURCE:
Rabbit anti-AIF (CT) polyclonal antibody was raised against
a peptide (KDGEQHEDLNEVAK) corresponding to amino
acids 593 to 606 of human AIF (2). This sequence is
identical to those of mouse and rat AIF (2).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of AIF in
K562 cell lysate (A), mouse (B),
and rat (C) liver tissue lysates
with anti-AIF (CT) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2301P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
REFERENCES:
1. Zamzami N, Kroemer G. Condensed matter in cell death. Nature
1999;401:127-8
2. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular
characterization of mitochondrial apoptosis-inducing factor. Nature
1999;397:441-6
(WD0800)
APPLICATION:
This polyclonal antibody can be used for detection of AIF by
Western blot at 0.25 to 1 µg/ml. K562 cell lysate can be used
as positive control and a 67 kDa band should be detected. It
is human, mouse, and rat reactive. For research use only.

13100 Kirkham Way
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Toll Free: 888-513-9525
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Fax: 858-513-2692
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Anti-DAP Kinase 2
CATALOG No.: 2323
BACKGROUND:
Apoptosis is mediated by death domain containing adapter
molecules and a caspase family of proteases. Certain
serine/threonine protein kinases, such as RIP and DAP
kinase, are mediators of apoptosis. DAP kinase (DAPK) is
pro-apoptotic calcium-regulated serine/threonine kinase
containing death domain. Ectopic expression of DAPK
induces cell death and suppresses oncogenic
transformation. DAPK mediates IFNγ induced apoptosis. A
novel DAP kinase-related protein was recently identified and
designated DAPK2 and DRP-1 (1, 2). Ectopicly expressed
DAPK2 induced apoptosis in various types of cells (1,2).
DAPK has high sequence homology to ZIP kinase and
DRAK1/2, and they represent a novel family of
serine/threonine kinases, which mediates apoptosis through
their catalytic activities. The messenger RNA of DAPK2 is
expressed in multiple human tissues (1).
SOURCE:
Rabbit anti-DAPK2 polyclonal antibody was raised against a
peptide (ARRKALHPRRRSSTS) corresponding to amino
acids 356 to 370 of human DAPK2 (1,2). The sequence of
this antigenic peptide is identical to the corresponding amino
acids of mouse origin (1,2)
APPLICATION:
This polyclonal antibody can be used for detection of DAPK2
by Western blot at 0.5 to 1 µg/ml. A431 whole cell lysate can
be used as positive control and an approximately 42 kDa
band can be detected. It is human, mouse, and rat reactive,
and has no cross responses to DAPK1. For research use
only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
DAPK2 in A431 (H), mouse
spleen (M), and rat kidney (R)
lysates with anti-DAPK2
(2323) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2323P).
A431 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1202).
REFERENCES:
1. Kawai T, Nomura F, Hoshino K, Copeland NG, Gilbert DJ,
Jenkins NA, Akira S. Death-associated protein kinase 2 is a new
calcium/calmodulin-dependent protein kinase that signals
apoptosis through its catalytic activity. Oncogene
1999;18(23):3471-80
2. Inbal B, Shani G, Cohen O, Kissil JL, Kimchi A. Deathassociated
protein kinase-related protein 1, a novel
serine/threonine kinase involved in apoptosis. Mol Cell Biol
2000;20(3):1044-54
(WD0101)

13100 Kirkham Way
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Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-Caspase-12 (NT)
CATALOG No.: 2325
BACKGROUND:
Three distinct signaling pathways lead to programmed cell
death (apoptosis). The death receptor and mitochondrion
pathways are the mains, in which the key apoptotic
proteases capase-8 and caspase-9, respectively, are
involved. The endoplasmic reticulum (ER) stress is the third
apoptotic pathway and caspase-12 is involved (1,2).
Caspase-12 is localized to the ER but not to cytoplasm or
mitochondrion. Caspase-12 is activated by ER stress,
including disruption of ER calcium homeostasis, and
mediates ER stress-induced apoptosis. Caspase-12 is colocalized
to the ER with several proteins that are involved in
Alzheimer’s disease including γ-secretase presenilin and β-
amyloid precursor protein (APP). Caspase-12 mediates
cytotoxicity induced by amyloid-β. Caspase-12 is
ubiquitously expressed in mouse tissues (1).
SOURCE:
Rabbit anti-caspase-12 (NT) polyclonal antibody was raised
against a peptide (AARRTHERDPIYKIKG) corresponding
to amino acids 2 to 17 of murine caspase-12 (3).
APPLICATION:
This polyclonal antibody can be used for detection of
caspase-12 by Western blot at 0.5 to 1 µg/ml. Murine spleen
tissue lysate can be used as positive control. It is human,
mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
caspase-12 in human (A)
and mouse (B) spleen
tissue lysates with anticaspase-12
(NT) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2325P).
Murine spleen tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1406).
REFERENCES:
1. Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA,
Yuan J. Caspase-12 mediates endoplasmic-reticulum-specific
apoptosis and cytotoxicity by amyloid-beta. Nature 2000;403:98-
103.
2. Mehmet H. Caspases find a new place to hide. Nature
2000;403:29-30
3. Van de Craen M, Vandenabeele P, Declercq W, Van den
Brande I, Van Loo G, Molemans F, Schotte P, Van Criekinge W,
Beyaert R, Fiers W. Characterization of seven murine caspase
family members. FEBS Lett 1997;403:61-9
(WD1000)

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Anti-Caspase-12 (IN)
CATALOG No.: 2327
BACKGROUND:
Three distinct signaling pathways lead to programmed cell
death (apoptosis). The death receptor and mitochondrion
pathways are the mains, in which the key apoptotic
proteases capase-8 and caspase-9, respectively, are
involved. The endoplasmic reticulum (ER) stress is the third
apoptotic pathway and caspase-12 is involved (1,2).
Caspase-12 is localized to the ER but not to cytoplasm or
mitochondrion. Caspase-12 is activated by ER stress,
including disruption of ER calcium homeostasis, and
mediates ER stress-induced apoptosis. Caspase-12 is colocalized
to the ER with several proteins that are involved in
Alzheimer’s disease including γ-secretase presenilin and β-
amyloid precursor protein (APP). Caspase-12 mediates
cytotoxicity induced by amyloid-β. Caspase-12 is
ubiquitously expressed in mouse tissues (1).
SOURCE:
Rabbit anti-caspase-12 (IN) polyclonal antibody was raised
against a peptide (CTPSSPSESKRKVEDDE) corresponding
to amino acids 100 to 116 of murine caspase-12 (3).
APPLICATION:
This polyclonal antibody can be used for detection of
caspase-12 by Western blot at 0.5 to 1 µg/ml. Murine brain
tissue lysate can be used as positive control. It is human,
mouse, and rat reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
caspase-12 in murine brain
tissue lysate in the absence
(A) or presence (B) of
blocking peptide with anticaspase-12
(IN) at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2327P).
Murine brain tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1403).
REFERENCES:
1. Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA,
Yuan J. Caspase-12 mediates endoplasmic-reticulum-specific
apoptosis and cytotoxicity by amyloid-beta. Nature 2000;403:98-
103.
2. Mehmet H. Caspases find a new place to hide. Nature
2000;403:29-30
3. Van de Craen M, Vandenabeele P, Declercq W, Van den
Brande I, Van Loo G, Molemans F, Schotte P, Van Criekinge W,
Beyaert R, Fiers W. Characterization of seven murine caspase
family members. FEBS Lett 1997;403:61-9
(WD0900)

13100 Kirkham Way
Suite 207
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www.prosci-inc.com
Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IKKε / IKK-i (CT)
CATALOG No.: 2329
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli. NF-κB is associated with
IκB proteins in the cell cytoplasm, which inhibit NF-κB
activity. IκB is phosphorylated by IκB kinase (IKK) complex
that contains IKKα, IKKβ, and IKKγ. A novel molecule in the
IKK complex was recently identified and designated
IKKε/IKK-i (1,2). IKKε is required for the activation of NF-κB
by PMA and T cell receptors but not by TNFα and IL-1 (1).
IKKε/IKK-i message is expressed in a variety of tissues and
is inducible by TNFα, IL-1, and LPS (2).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
Western blot analysis of
IKKε in Jurkat whole cell
lysate with anti-IKKε/IKK-i
at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2329P).
SOURCE:
Rabbit anti-IKKε polyclonal antibody was raised against a
peptide (NRIIERLNRVPAPPDV) corresponding to amino
acids 701 to 716 of human IKKε/IKK-i (1,2).
APPLICATION:
This polyclonal antibody can be used for detection of IKKε by
Western blot at 0.5 to 1 µg/ml. Jurkat whole cell lysate can
be used as positive control and an 80 kDa band should be
detected. It has no cross response to IKKα, IKKβ, or IKKγ.
For research use only.
REFERENCES:
1. Peters RT, Liao SM, Maniatis T. IKKepsilon is part of a novel
PMA-inducible IkappaB kinase complex. Mol Cell 2000;5(3):513-22
2. Shimada T, Kawai T, Takeda K, Matsumoto M, Inoue J, Tatsumi
Y, Kanamaru A, Akira S. IKK-i, a novel lipopolysaccharideinducible
kinase that is related to IkappaB kinases. Int Immunol
1999;11(8):1357-62
(WD0101)

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Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IKKγ / NEMO (NT)
CATALOG No.: 2335
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli. NF-κB is associated with
IκB proteins in the cell cytoplasm, which inhibit NF-κB
activity. The IκB kinase (IKKα and IKKβ) phosphorylates IκB
and mediates NF-κB activation. A novel molecule in the IKK
complex was recently identified and termed
IKKγ/NEMO/FIP3/IKKAP1 (1-5). IKKγ interacts with IKKβ and
is required for the activation of IKK complex and NF-κB by
LPS, PMA, TNF, and IL-1 stimulation (1-4). FIP3 was also
shown to bind to RIP and NIK and to mediate TNF-induced
NF-κB activation (3).
SOURCE:
Rabbit anti-IKKγ polyclonal antibody was raised against a
peptide (CQYQAPDMDTLQIHVME) corresponding to amino
acids 400 to 416 of human IKKγ (1,2), which are identical to
those of mouse homologue (2).
APPLICATION:
This polyclonal antibody can be used for detection of IKKγ by
Western blot at 0.5 to 1 µg/ml. HeLa whole cell lysate can be
used as positive control and a 52 kDa band should be
detected. It is human, mouse, and rat reactive and has no
cross response to IKKα or IKKβ. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2335P).
Western blot analysis of IKKγ
in HeLa whole cell lysate with
anti-IKKγ/NEMO at 1 µg/ml.
REFERENCES:
1. Rothwarf DM, Zandi E, Natoli G, Karin M. IKK-gamma is an
essential regulatory subunit of the IkappaB kinase complex. Nature
1998;395(6699):297-300
2. Yamaoka S, Courtois G, Bessia C, Whiteside ST, Weil R, Agou
F, Kirk HE, Kay RJ, Israel A. Complementation cloning of NEMO, a
component of the IkappaB kinase complex essential for NFkappaB
activation. Cell. 1998;93(7):1231-40.
3. Li Y, Kang J, Friedman J, Tarassishin L, Ye J, Kovalenko A,
Wallach D, Horwitz MS. Identification of a cell protein (FIP-3) as a
modulator of NF-kappaB activity and as a target of an adenovirus
inhibitor of tumor necrosis factor alpha-induced apoptosis. Proc
Natl Acad Sci U S A 1999;96(3):1042-7
4. Mercurio F, Murray BW, Shevchenko A, Bennett BL, Young DB,
Li JW, Pascual G, Motiwala A, Zhu H, Mann M, Manning AM.
IkappaB kinase (IKK)-associated protein 1, a common component
of the heterogeneous IKK complex. Mol Cell Biol.
1999;19(2):1526-38.
5. Jin DY, Jeang KT. Isolation of full-length cDNA and
chromosomal localization of human NF-kappaB modulator NEMO
to Xq28. J Biomed Sci 1999;6(2):115-20
(WD0101)

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Anti-DC-SIGN (CT)
CATALOG No.: 2347
BACKGROUND:
Dendritic cells (DCs) that control immune responses were
recently found to capture and transport HIV from the
mucosal area to remote lymph nodes (1), where DCs hand
over HIV to CD4 + T lymphocytes. DCs also amplify the
amount of virus and extend the duration of viral infectivity.
Multiple strains of HIV-1, HIV-2 and SIV bind to DCs via DC-
SIGN (2). ICAM-3 is the natural ligand for DC-SIGN (3). A
DC-SIGN homologue (termed DC-SIGNR, L-SIGN, and DC-
SIGN2) was identified recently (4-8). DC-SIGN forms a novel
gene family with DC-SIGNR and many alternatively spliced
isoforms of DC-SIGN and DC-SIGNR (8). The expression of
DC-SIGN was found in mucosal tissues including placenta,
small intestine, and rectum.
SOURCE:
Rabbit anti-DC-SIGN polyclonal antibody was raised against
a synthetic peptide (CSRDEEQFLSPAPATPN PPPA)
corresponding to amino acids 384 to 404 of human DC-
DIGN (1).
APPLICATION:
This antibody can be used for detection of DC-SIGN by
Western blot at 1 to 2 µg/ml. Human placenta lysate can be
used as a positive control. A band at approximately 44 kDa
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2347P).
Human placenta lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1309).
Western blot detection of
GST-DC-SIGN
fusion
protein expressed in E. Coli
in the absence (lane 1) and
presence (lane 2) of
inducing reagent IPTG with
anti-DC-SIGN at 0.5 µg /ml.
REFERENCES:
1. Geijtenbeek TB, Kwon DS, Torensma R, et al. DC-SIGN, a
dendritic cell-specific HIV -1-binding protein that enhances transinfection
of T cells. Cell. 2000;100:587-97.
2. Pohlmann S, Baribaud F, Lee B, et al. RW. DC-SIGN
interactions with human immunodeficiency virus type 1 and 2 and
simian immunodeficiency virus. J Virol. 2001;75(10):4664-72.
3. Geijtenbeek TB, Torensma R, van Vliet SJ, et al. Identification
of DC-SIGN, a novel dendritic cell-specific ICAM-3 receptor that
supports primary immune responses. Cell. 2000;100(5):575-85.
4. Soilleux EJ, Barten R, Trowsdale J. DC-SIGN; a related gene,
DC-SIGNR; and CD23 form a cluster on 19p13. J Immunol.
2000;165(6):2937-42.
5. Pohlmann S, Soilleux EJ, Baribaud F, et al DC-SIGNR, a DC-
SIGN homologue expressed in endothelial cells, binds to human
and simian immunodeficiency viruses and activates infection in
trans. Proc Natl Acad Sci USA. 2001;98(5):2670-2675.
6. Bashirova AA, Geijtenbeek TB, van Duijnhoven GC, at el. A
dendritic cell-specific intercellular adhesion molecule 3-grabbing
nonintegrin (DC-SIGN)-related protein is highly expressed on
human liver sinusoidal endothelial cells and promotes HIV -1
infection. J Exp Med. 2001;193(6):671-8.
7. Mitchell DA, Fadden AJ, Drickamer K. A novel mechanism of
carbohydrate recognition by the C-type lectins DC-SIGN and DC-
SIGNR: Subunit organisation and binding to multivalent ligands. J
Biol Chem. 2001 in press
8. Mummidi S, Catano G, Lam L, et al. Extensive repertoire of
membrane-bound and soluble DC-SIGN1 and DC-SIGN2 isoforms:
Inter-individual variation in expression of DC-SIGN transcripts. J
Biol Chem. 2001 in press
(WD0108)

13100 Kirkham Way
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www.prosci-inc.com
Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-DC-SIGN (ED)
CATALOG No.: 2349
BACKGROUND:
Dendritic cells (DCs) that control immune responses were
recently found to capture and transport HIV from the
mucosal area to remote lymph nodes (1), where DCs hand
over HIV to CD4 + T lymphocytes. DCs also amplify the
amount of virus and extend the duration of viral infectivity.
Multiple strains of HIV-1, HIV-2 and SIV bind to DCs via DC-
SIGN (2). ICAM-3 is the natural ligand for DC-SIGN (3). A
DC-SIGN homologue (termed DC-SIGNR, L-SIGN, and DC-
SIGN2) was identified recently (4-8). DC-SIGN forms a novel
gene family with DC-SIGNR and many alternatively spliced
isoforms of DC-SIGN and DC-SIGNR (8). The expression of
DC-SIGN was found in mucosal tissues including placenta,
small intestine, and rectum.
SOURCE:
Rabbit anti-DC-SIGN polyclonal antibody was raised against
a synthetic peptide (CYFMSNSQRN WHDSITA)
corresponding to amino acids 277 to 293 of human DC-
DIGN (1).
APPLICATION:
This antibody can be used for detection of DC-SIGN by
Western blot at 1 to 2 µg/ml. Human placenta lysate can be
used as a positive control. A band at approximately 44 kDa
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2349P).
Human placenta lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1309).
Western blot analysis of DC-
SIGN expression in human
placenta tissue lysate in the
absence (lane 1) and presence
(lane 2) of blocking peptide with
anti-DC-SIGN at 2 µg /ml.
REFERENCES:
1. Geijtenbeek TB, Kwon DS, Torensma R, et al. DC-SIGN, a
dendritic cell-specific HIV -1-binding protein that enhances transinfection
of T cells. Cell. 2000;100:587-97.
2. Pohlmann S, Baribaud F, Lee B, et al. RW. DC-SIGN
interactions with human immunodeficiency virus type 1 and 2 and
simian immunodeficiency virus. J Virol. 2001;75(10):4664-72.
3. Geijtenbeek TB, Torensma R, van Vliet SJ, et al. Identification
of DC-SIGN, a novel dendritic cell-specific ICAM-3 receptor that
supports primary immune responses. Cell. 2000;100(5):575-85.
4. Soilleux EJ, Barten R, Trowsdale J. DC-SIGN; a related gene,
DC-SIGNR; and CD23 form a cluster on 19p13. J Immunol.
2000;165(6):2937-42.
5. Pohlmann S, Soilleux EJ, Baribaud F, et al DC-SIGNR, a DC-
SIGN homologue expressed in endothelial cells, binds to human
and simian immunodeficiency viruses and activates infection in
trans. Proc Natl Acad Sci USA. 2001;98(5):2670-2675.
6. Bashirova AA, Geijtenbeek TB, van Duijnhoven GC, at el. A
dendritic cell-specific intercellular adhesion molecule 3-grabbing
nonintegrin (DC-SIGN)-related protein is highly expressed on
human liver sinusoidal endothelial cells and promotes HIV -1
infection. J Exp Med. 2001;193(6):671-8.
7. Mitchell DA, Fadden AJ, Drickamer K. A novel mechanism of
carbohydrate recognition by the C-type lectins DC-SIGN and DC-
SIGNR: Subunit organisation and binding to multivalent ligands. J
Biol Chem. 2001 in press
8. Mummidi S, Catano G, Lam L, et al. Extensive repertoire of
membrane-bound and soluble DC-SIGN1 and DC-SIGN2 isoforms:
Inter-individual variation in expression of DC-SIGN transcripts. J
Biol Chem. 2001 in press
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
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techsupport@prosci-inc.com
Anti-NAK / TBK1 (CT)
CATALOG No.: 2351
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli. NF-κB is associated with
IκB proteins in the cell cytoplasm, which inhibit NF-κB
activity. Phosphorylation of I-κB by IκB kinase (IKK) complex
leads to degradation of I-κB and activation of NF-κB. The
IKK complex contains IKKα, IKKβ, and IKKγ. A novel IKK
related kinase was recently identified and designated TBK1
(TANK-binding kinase 1), NAK (NF-κB-activating kinase),
and T2K (1-3). NAK/TBK1 activates IKKβ through direct
phosphorylation. NAK/TBK1 is activated by growth factors
and PMA and mediates IKK and NF-kB activation in
response to growth factors (2). NAK/TBK1 functions
upstream of NIK and the IKK complex (1,2). NAK/TBK1 is
also critical in protecting embryonic liver from apoptosis (3).
SOURCE:
Rabbit anti-NAK/TBK1 polyclonal antibody was raised
against a synthetic peptide (ERFGSLTMDGGLRNVD)
corresponding to amino acids 712 to 727 of human
NAK/TBK1 (1,2), which are identical to those of mouse
homologue (1).
STORAGE:
It is supplied as immunoaffinity chromatography purified
IgG, 100 µg in 200 µl of PBS containing 0.02% sodium
azide. Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2351P).
REFERENCES:
1. Pomerantz JL, Baltimore D. NF-kappaB activation by a
signaling complex containing TRAF2, TANK and TBK1, a novel
IKK-related kinase. EMBO J 1999;18(23):6694-704
2. Tojima Y, Fujimoto A, Delhase M, Chen Y, Hatakeyama S,
Nakayama K, Kaneko Y, Nimura Y, Motoyama N, Ikeda K, Karin
M, Nakanishi M. NAK is an IkappaB kinase-activating kinase.
Nature 2000;404(6779):778-82
3. Bonnard M, Mirtsos C, Suzuki S, Graham K, Huang J, Ng M, Itie
A, Wakeham A, Shahinian A, Henzel WJ, Elia AJ, Shillinglaw W,
Mak TW, Cao Z, Yeh WC. Deficiency of T2K leads to apoptotic
liver degeneration and impaired NF-kappaB-dependent gene
transcription. EMBO J. 2000;19(18):4976-85.
(WD0101)
APPLICATION:
This polyclonal antibody can be used for detection of
NAK/TBK1 by Western blot at 0.5 to 1 µg/ml. MOLT4 whole
cell lysate can be used as positive control and an 84 kDa
band should be detected. It is human, mouse and rat
reactive and has no cross response to IKKα, IKKβ, IKKγ, or
IKKε. For research use only.

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Anti-IRAK-M
CATALOG No.: 2355
BACKGROUND:
Interleukin-1 (IL-1) and lipopolysaccharide (LPS) induces
cellular response through IL-1 receptor (IL-1R) and Toll like
receptors (TLR). IL-1 receptor-associated kinase (IRAK and
IRAK2) mediates the activation of NF-κB by IL-1/Toll
receptors (1,2), which is a pivotal transcription factor
mediating inflammatory and immune response. A novel
member in the IRAK/Pelle family was recently identified and
designated IRAK-M (3). IRAKs associate with IL-1/Toll
receptors after IL-1 or LPS stimulation and the dominant
negative mutants of IRAKs inhibit IL-1 or LPS induced NFκB
activation. Members in IRAK/Pelle family play a central
role in IL-1R/TLR mediated inflammatory responses to
cytokine IL-1 and LPS.
STORAGE:
It is supplied as chromatography purified IgG, 100 µg in
200 µl of PBS containing 0.02% sodium azide. Store at
4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2355P).
Murine spleen tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1406).
Western blot analysis of
IRAK-M in mouse spleen (M)
and rat liver (R) tissue lysates
with anti-IRAK-M at 1 µg /ml.
SOURCE:
Rabbit anti-IRAK-M polyclonal antibody was raised against a
peptide (CSSKFSWDEYEQYKKE) corresponding to amino
acids 581 to 596 of human IRAK-M (3).
APPLICATION:
This polyclonal antibody can be used for detection of IRAK-
M by Western blot at 0.5 to 1 µg/ml. Mouse spleen or rat
kidney tissue lysate can be used as positive control and a 68
kDa major band can be detected. It is human, mouse, and
rat reactive. Anti-IRAK-M has no cross response to IRAK or
IRAK2. For research use only.
REFERENCES:
1. Cao Z; Henzel WJ; Gao X. IRAK: a kinase associated with the
interleukin-1 receptor. Science 1996;271:1128-31.
2. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member
IRAK-2 and MyD88 as proximal mediators of IL-1 signaling.
Science 1997;278:1612-5
3. Wesche H, Gao X, Li X, Kirschning CJ, Stark GR, Cao Z. IRAK-
M is a novel member of the Pelle/interleukin-1 receptor-associated
kinase (IRAK) family. J Biol Chem. 1999;274(27):19403-10.
(WD0101)

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Toll Free: 888-513-9525
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Anti-p53R2 (NT)
CATALOG No.: 2383
BACKGROUND:
The p53 tumor-suppressor gene integrates numerous
signals that control cell life and death. Several novel
molecules involved in p53 signaling, including p53R2 (1),
Chk2 (2), p53AIP1 (3), Noxa (4), PIDD (5), and PID/MTA2
(6), were recently discovered. p53R2 is a p53 inducible gene
that contains a p53 binding sequence and encodes a subunit
of the enzyme ribonucleotide reductase (1,7). p53R2 is
induced by the reagents, ultraviolet and γ-irradiation that
cause DNA damages. The product of p53R2 gene is directly
involved in the p53 checkpoint for repair of damaged DNA.
The isoform of the p53 family member p73 also induces
p53R2 expression (8). p53R2 is an important target of p53
for tumour suppression.
SOURCE:
Rabbit anti-p53R2 polyclonal antibody was raised against a
synthetic peptide (GDPERPEAAGLDQDER) corresponding
to amino acids 2 to 17 of human p53R2 (1).
APPLICATION:
This antibody can be used for detection of p53R2 by
Western blot at 0.5 to 1 µg/ml. A431 or 3T3 cell lysate can
be used as positive control and a 39 kDa band can be
detected. It is human, mouse, and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2383P).
A431 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1202).
Western blot analysis of p53R2
expression in A431 (A) and 3T3
cell lysates in the absence (B) or
presence (C) of blocking peptide
with anti-p53R2 at 1 µg /ml.
REFERENCES:
1. Tanaka H, Arakawa H, Yamaguchi T, Shiraishi K, Fukuda S, Matsui K,
Takei Y, Nakamura Y. A ribonucleotide reductase gene involved in a p53-
dependent cell-cycle checkpoint for DNA damage. Nature. 2000;404:42-9.
2. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle
regulation by the Chk2 protein kinase. Science. 1998;282:1893-7.
3. Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita T, Tokino T,
Taniguchi T, Tanaka N. Noxa, a BH3-only member of the Bcl-2 family and
candidate mediator of p53-induced apoptosis. Science.
2000;288(5468):1053-8.
4. Oda K, Arakawa H, Tanaka T, Matsuda K, Tanikawa C, Mori T, Nishimori
H, Tamai K, Tokino T, Nakamura Y, Taya Y. p53AIP1, a potential mediator
of p53-dependent apoptosis, and its regulation by Ser-46-phosphorylated
p53. Cell. 2000 Sep 15;102(6):8 49-62.
5. Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53 modulates its
effect on cell growth and apoptosis.
Nature. 2000;408:377-81.
6. Lin Y, Ma W, Benchimol S. Pidd, a new death-domain-containing protein,
is induced by p53 and promotes apoptos is. Nat Genet. 2000;26:122-7.
7. Lozano G, Elledge SJ. p53 sends nucleotides to repair DNA. Nature.
2000;404:24-5.
8. Nakano K, Balint E, Ashcroft M, Vousden KH. A ribonucleotide reductase
gene is a transcriptional target of p53 and p73. Oncogene.
2000;19(37):4283-9. (WD0105)

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Anti-Chk2 (NT)
CATALOG No.: 2391
BACKGROUND:
The p53 tumor-suppressor gene integrates numerous
signals that control cell life and death. Several novel
molecules involved in p53 signaling, including Chk2 (1),
p53R2 (2), p53AIP1 (3), Noxa (4), PIDD (5), and PID/MTA2
(6), were recently discovered. The checkpoint kinase Chk2 is
the mammalian homologue of yeast Cds1/Rad53. In
response to DNA damage, the checkpoint kinase ATM
phosphorylates and activates Chk2, which in turn directly
phosphorylates and activates p53 (7,8). Chk2 serves as
ATM downstream effector to mediate activation of p53. Chk2
also phosphorylates and activates BRCA1, the product of a
tumor suppressor gene that is mutated in breast and ovarian
cancer (9).
SOURCE:
Rabbit anti-Chk2 polyclonal antibody was raised against a
synthetic peptide (SRESDVEAQQSHGSSAC) corresponding
to amino acids 2 to 18 of human Chk2 (1).
APPLICATION:
This antibody can be used for detection of Chk2 by Western
blot at 0.5 to 1 µg/ml. Jurkat or K562 cell lysate can be used
as positive control and a 60 kDa band can be detected. It is
human, mouse, and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2391P).
Jurkat cell lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1205).
Western blot analysis of
Chk2 expression in K562
(A), Jurkat (B), and HL-60
(C) whole cell lysates with
anti-Chk2 at 1 µg /ml.
REFERENCES:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell
cycle regulation by the Chk2 protein kinase. Science.
1998;282:1893-7.
2. Tanaka H, Arakawa H, Yamaguchi T, Shiraishi K, Fukuda S,
Matsui K, Takei Y, Nakamura Y. A ribonucleotide reductase gene
involved in a p53-dependent cell-cycle checkpoint for DNA
damage. Nature. 2000;404:42-9.
3. Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita
T, Tokino T, Taniguchi T, Tanaka N. Noxa, a BH3-only member of
the Bcl-2 family and candidate mediator of p53-induced
apoptosis. Science. 2000;288(5468):1053-8.
4. Oda K, Arakawa H, Tanaka T, Matsuda K, Tanikawa C, Mori T,
Nishimori H, Tamai K, Tokino T, Nakamura Y, Taya Y. p53AIP1, a
potential mediator of p53-dependent apoptosis, and its regulation
by Ser-46-phosphorylated p53. Cell. 2000 Sep 15;102(6):849-62.
5. Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53
modulates its effect on cell growth and apoptosis.
Nature. 2000;408:377-81.
6. Lin Y, Ma W, Benchimol S. Pidd, a new death-domaincontaining
protein, is induced by p53 and promotes apoptosis.
Nat Genet. 2000;26:122-7.
7. Matsuoka S, Rotman G, Ogawa A, Shiloh Y, Tamai K, Elledge
SJ. Ataxia telangiectasia-mutated phosphorylates Chk2 in vivo
and in vitro.Proc Natl Acad Sci USA. 2000 ;97:10389-94.
8. Hirao A, Kong YY, Matsuoka S, Wakeham A, Ruland J,
Yoshida H, Liu D, Elledge SJ, Mak TW. DNA damage-induced
activation of p53 by the checkpoint kinase Chk2. Science.
2000;287:1824-7
9. Lee JS, Collins KM, Brown AL, Lee CH, Chung JH. hCds1-
mediated phosphorylation of BRCA1 regulates the DNA damage
response. Nature. 2000;404:201-4.
(WD0105)

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Anti-Smac / DIABLO (CT)
CATALOG No.: 2409
BACKGROUND:
The inhibitor of apoptosis proteins (IAPs) regulate
programmed cell death by inhibiting members of the caspase
family of enzymes. A novel mammalian protein that binds to
IAPs and neutralizes the inhibitory effect of IAPs on
caspases was recently identified and designated
Smac/DIABLO (1,2). Smac/DIABLO is a mitochondrial
protein that is released along with cytochrome c during
apoptosis and activates cytochrome c/Apaf-1/capase-9
pathway. Analysis of the structural basis of Smac/DIABLO
reveals that the N-terminal amino acids are required for
binding of Smac/DIABLO to IAPs and activation of caspases
(3-6). Smac/DIABLO is expressed in a variety of human and
mouse tissues (1,2).
SOURCE:
Rabbit anti-Smac/DIABLO (CT) polyclonal antibody was
raised against a peptide (EERAESEQEAYLRED)
corresponding to amino acids 225 to 239 of human
Smac/DIABLO (1).
APPLICATION:
This polyclonal antibody can be used for detection of
Smac/DIABLO by Western blot at 0.5 to 1 µg/ml. Human
heart tissue lysate can be used as positive control and a 25
kDa band can be detected. It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2409P). Human heart tissue
lysate, 200 µg at 2 mg/ml, is available for positive control
(Catalog No. 1301).
Western blot analysis of Smac
in human heart tissue lysate in
the absence (A) or presence (B)
of blocking peptide (2409P) with
anti-Smac at 1 µg /ml.
REFERENCES:
1. Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein
that promotes cytochrome c-dependent caspase activation by
eliminating IAP inhibition. Cell. 2000;102(1):33-42.
2. Verhagen AM, Ekert PG, Pakusch M, Silke J, Connolly LM, Reid
GE, Moritz RL, Simpson RJ, Vaux DL. Identification of DIABLO, a
mammalian protein that promotes apoptosis by binding to and
antagonizing IAP proteins. Cell. 2000;102(1):43-53.
3. Srinivasula SM, Datta P, Fan XJ, Fernandes-Alnemri T, Huang Z,
Alnemri ES. Molecular Determinants of the Caspase-promoting
Activity of Smac/DIABLO and Its Role in the Death Receptor
Pathway. J Biol Chem. 2000;275(46):36152-36157.
4. Chai J, Du C, Wu JW, Kyin S, Wang X, Shi Y. Structural and
biochemical basis of apoptotic activation by Smac/DIABLO. Nature.
2000;406(6798):855-62.
5. Liu Z, Sun C, Olejniczak ET, Meadows RP, Betz SF, Oost T,
Herrmann J, Wu JC, Fesik SW. Structural basis for binding of
Smac/DIABLO to the XIAP BIR3 domain. Nature.
2000;408(6815):1004-8.
6. Wu G, Chai J, Suber TL, Wu JW, Du C, Wang X, Shi Y. Structural
basis of IAP recognition by Smac/DIABLO. Nature.
2000;408(6815):1008-12.
(WD0102)

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Anti-mSmac / DIABLO (CT)
CATALOG No.: 2411
BACKGROUND:
The inhibitor of apoptosis proteins (IAPs) regulate
programmed cell death by inhibiting members of the caspase
family of enzymes. A novel mammalian protein that binds to
IAPs and neutralizes the inhibitory effect of IAPs on
caspases was recently identified and designated
Smac/DIABLO (1,2). Smac/DIABLO is a mitochondrial
protein that is released along with cytochrome c during
apoptosis and activates cytochrome c/Apaf-1/capase-9
pathway. Analysis of the structural basis of Smac/DIABLO
reveals that the N-terminal amino acids are required for
binding of Smac/DIABLO to IAPs and activation of caspases
(3-6). Smac/DIABLO is expressed in a variety of human and
mouse tissues (1,2).
SOURCE:
Rabbit anti-mSmac/DIABLO (CT) polyclonal antibody was
raised against a peptide (SDEGADQEEEAYLRED)
corresponding to amino acids 222 to 237 of murine
Smac/DIABLO (2).
APPLICATION:
This polyclonal antibody can be used for detection of
Smac/DIABLO by Western blot at 0.5 to 1 µg/ml. mouse
heart tissue lysate can be used as positive control and a 25
kDa band can be detected. It is human, mouse, and rat
reactive. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2411P). Mouse heart
tissue lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1401).
Western blot analysis of Smac in
mouse heart tissue lysate in the
absence (A) or presence (B) of
blocking peptide (2411P) and in
rat heart tissue lysate with antimSmac
at 1 µg /ml.
REFERENCES:
1. Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein
that promotes cytochrome c-dependent caspase activation by
eliminating IAP inhibition. Cell. 2000;102(1):33-42.
2. Verhagen AM, Ekert PG, Pakusch M, Silke J, Connolly LM, Reid
GE, Moritz RL, Simpson RJ, Vaux DL. Identification of DIABLO, a
mammalian protein that promotes apoptosis by binding to and
antagonizing IAP proteins. Cell. 2000;102(1):43-53.
3. Srinivasula SM, Datta P, Fan XJ, Fernandes-Alnemri T, Huang
Z, Alnemri ES. Molecular Determinants of the Caspase-promoting
Activity of Smac/DIABLO and Its Role in the Death Receptor
Pathway. J Biol Chem. 2000;275(46):36152-36157.
4. Chai J, Du C, Wu JW, Kyin S, Wang X, Shi Y. Structural and
biochemical basis of apoptotic activation by Smac/DIABLO.
Nature. 2000;406(6798):855-62.
5. Liu Z, Sun C, Olejniczak ET, Meadows RP, Betz SF, Oost T,
Herrmann J, Wu JC, Fesik SW. Structural basis for binding of
Smac/DIABLO to the XIAP BIR3 domain. Nature.
2000;408(6815):1004-8.
6. Wu G, Chai J, Suber TL, Wu JW, Du C, Wang X, Shi Y.
Structural basis of IAP recognition by Smac/DIABLO. Nature.
2000;408(6815):1008-12.
(WD0102)

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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-APRIL (ED2) TALL-2, TRDL-1
CATALOG No.: 2415
BACKGROUND:
Members in the TNF superfamily regulate immune
responses and induce apoptosis. A novel member in the
TNF family was recently identified by several groups and
designated APRIL (for a proliferation-inducing ligand), TALL-
2 (for TNF- and ApoL-related Leukocyte-expressed Ligand
2), and TRDL-1α (for TNF related death ligand 1α) in human
and mouse (1-4). Two receptors for APRIL were recently
identified and designated TACI and BCMA (5-7). APRIL
stimulates B and T cell proliferation, triggers humoral
immune responses, activates NF-kB, and induces cell death
(1-7). APRIL and its close relative of BlyS and their
receptors BCMA and TACI are involved in diseases of
autoimmunity and cancer (8,9).
SOURCE:
Rabbit anti-APRIL (ED2) polyclonal antibody was raised
against a synthetic peptide (CIRSMPSHPDRAYNS)
corresponding to amino acids 196 to 210 of human APRIL
(1-3).
APPLICATION:
This antibody can be used for detection of APRIL by
Western blot at 2-4 µg/ml. HL60 or Jurkat cell lysate can be
used as positive control and an approximately 42 kDa band
can be detected. For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 200 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCT:
Blocking peptide, 50 µg/250 µl, is available for competition
studies (Catalog No. 2415P).
HL60 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1209).
Western blot analysis of APRIL
expression in Jurkat cell lysates
in the absence (A) or presence
(B) of blocking peptide with anti-
APRIL at 2 µg /ml.
REFERENCES:
1. Hahne M, Kataoka T, Schroter M, et al. APRIL, a new ligand of the tumor
necrosis factor family, stimulates tumor cell growth. J Exp Med.
1998;188(6):1185-90.
2. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the TNF
family that is down-regulated by mitogens. J Leukoc Biol. 1999;65(5):680-3.
3. Kelly K, Manos E, Jensen G, et al. APRIL/TRDL-1, a tumor necrosis
factor-like ligand, stimulates cell death. Cancer Res. 2000;60(4):1021-7.
4. Yu G, Boone T, Delaney J, et al. APRIL and TALL-I and receptors BCMA
and TACI: system for regulating humoral immunity. Nat Immunol.
2000;1(3):252-6.
5. Wu Y, Bressette D, Carrell JA, et a. Tumor necrosis factor (TNF) receptor
superfamily member TACI is a high affinity receptor for TNF family members
APRIL and BLyS. J Biol Chem. 2000;275(45):35478-85.
6. Marsters SA, Yan M, Pitti RM, et al. Interaction of the TNF homologues
BLyS and APRIL with the TNF receptor homologues BCMA and TACI. Curr
Biol. 2000;10(13):785-8.
7. Rennert P, Schneider P, Cachero TG, at al. A soluble form of B cell
maturation antigen, a receptor for the tumor necrosis factor family member
APRIL, inhibits tumor cell growth. J Exp Med. 2000;192(11):1677-84.
8. Gross JA, Johnston J, Mudri S, et al. TACI and BCMA are receptors for a
TNF homologue implicated in B-cell autoimmune disease. Nature
2000;404:995-9
9. Ware CF. APRIL and BAFF connect autoimmunity and cancer. J Exp
Med. 2000;192(11):F35-8.
(WD0105)

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Anti-PID / MTA2
CATALOG No.: 2443
BACKGROUND:
The p53 tumor-suppressor gene integrates numerous
signals that control cell life and death. Several novel
molecules involved in p53 pathway, including Chk2 (1),
p53R2 (2), p53AIP1 (3), Noxa (4), PIDD (5), and PID/MTA2
(6), were recently discovered. The transcriptional activity of
p53 is modulated by protein stability and acetylation.
PID/MTA2, also termed MTA1-L1, was found to be a subunit
of nucleosome remodeling and deacetylating (NRD/NuRD)
complex (6-8). PID/MTA2 modulates the enzymatic activity
of the histone deacetylase complex and its expression
reduces the levels of acetylated p53. Deacetylation of p53 by
PID/MTA2 represses p53-dependent transcriptional
activation and modulates p53-mediated cell growth arrest
and apoptosis (6). PID/MTA2 is ubiquitously expressed in
human tissues (8).
SOURCE:
Rabbit anti-PID/MTA2 polyclonal antibody was raised
against a synthetic peptide (PAPSHPASTNEPIVLED)
corresponding to amino acids 652 to 668 of human
PID/MTA2 (6), which differ from the mouse sequence by one
amino acid (7).
APPLICATION:
This antibody can be used for detection of PID/MTA2 by
Western blot at 0.5 to 1 µg/ml. HeLa cell lysate can be used
as positive control and a 75 kDa band can be detected. It is
human, mouse, and rat reactive and has no cross response
to MTA1. For research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2443P). HeLa cell lysate,
200 µg at 2 mg/ml, is available for positive control (Catalog
No. 1201).
Western blot analysis of
PID/MTA2 expression in HeLa
whole cell lysates in the absence
(A) or presence (B) of blocking
peptide with anti-PID at 1 µg /ml.
REFERENCES:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle
regulation by the Chk2 protein kinase. Science. 1998;282:1893-7.
2. Tanaka H, Arakawa H, Yamaguchi T, Shiraishi K, Fukuda S,
Matsui K, Takei Y, Nakamura Y. A ribonucleotide reductase gene
involved in a p53-dependent cell-cycle checkpoint for DNA
damage. Nature. 2000;404:42-9.
3. Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita T,
Tokino T, Taniguchi T, Tanaka N. Noxa, a BH3-only member of the
Bcl-2 family and candidate mediator of p53-induced apoptosis.
Science. 2000;288(5468):1053-8.
4. Oda K, Arakawa H, Tanaka T, Matsuda K, Tanikawa C, Mori T,
Nishimori H, Tamai K, Tokino T, Nakamura Y, Taya Y. p53AIP1, a
potential mediator of p53-dependent apoptosis, and its regulation
by Ser-46-phosphorylated p53. Cell. 2000 Sep 15;102(6):849-62.
5. Lin Y, Ma W, Benchimol S. Pidd, a new death-domaincontaining
protein, is induced by p53 and promotes apoptosis. Nat
Genet. 2000;26:122-7.
6. Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53
modulates its effect on cell growth and apoptosis. Nature.
2000;408:377-81.
7. Zhang Y, Ng HH, Erdjument-Bromage H, Tempst P, Bird A,
Reinberg D. Analysis of the NuRD subunits reveals a histone
deacetylase core complex and a connection with DNA methylation.
Genes Dev. 1999;13(15):1924-35.
8. Futamura M, Nishimori H, Shiratsuchi T, Saji S, Nakamura Y,
Tokino T.Molecular cloning, mapping, and characterization of a
novel human gene, MTA1-L1, showing homology to a metastasisassociated
gene, MTA1. J Hum Genet. 1999;44(1):52-6.
(WD0105)

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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-MTBP (IN2)
CATALOG No.: 2447
BACKGROUND:
The p53 tumor-suppressor gene integrates numerous
signals that control cell life and death. Several novel
molecules involved in p53 network, including Chk2 (1),
p53R2 (2), p53AIP1 (3), Noxa (4), PIDD (5), PID/MTA2 (6)
and MTBP (7), were recently discovered. The transcriptional
activity of p53 is modulated by posttranslational regulations
of the p53 protein including stabilization and acetylation. P53
transcriptionally activates MDM2 gene then the translated
MDM2 protein binds to p53 and promotes the degradation of
p53 leading to lowering the concentration of p53 protein.
MDM2 inhibits both p53 mediated G 1 arrest and apoptosis. A
recently discovered protein termed MTBP was found to bind
to MDM2 and to inhibit the modulation effect of MDM2 on
p53 (7). MTBP is expressed in a variety of normal tissues
(7).
SOURCE:
Rabbit anti-MTBP polyclonal antibody was raised against a
synthetic peptide (GAVECFEEEDSNSRESLS)
corresponding to amino acids 122 to 139 of human MTBP,
which differ from the mouse sequence by three amino acids
(7).
APPLICATION:
This antibody can be used for detection of MTBP by Western
blot at 0.5 to 1 µg/ml. K562 cell lysate can be used as
positive control and a 104 kDa band can be detected. For
research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2447P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1204).
Western blot analysis of
MTBP expression in K562
whole cell lysates with anti-
MTBP at 1 µg /ml.
REFERENCES:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle
regulation by the Chk2 protein kinase. Science. 1998;282:1893-7.
2. Tanaka H, Arakawa H, Yamaguchi T, Shiraishi K, Fukuda S,
Matsui K, Takei Y, Nakamura Y. A ribonucleotide reductase gene
involved in a p53-dependent cell-cycle checkpoint for DNA
damage. Nature. 2000;404:42-9.
3. Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita T,
Tokino T, Taniguchi T, Tanaka N. Noxa, a BH3-only member of the
Bcl-2 family and candidate mediator of p53-induced apoptosis.
Science. 2000;288(5468):1053-8.
4. Oda K, Arakawa H, Tanaka T, Matsuda K, Tanikawa C, Mori T,
Nishimori H, Tamai K, Tokino T, Nakamura Y, Taya Y. p53AIP1, a
potential mediator of p53-dependent apoptosis, and its regulation
by Ser-46-phosphorylated p53. Cell. 2000 Sep 15;102(6):849-62.
5. Lin Y, Ma W, Benchimol S. Pidd, a new death-domaincontaining
protein, is induced by p53 and promotes apoptosis. Nat
Genet. 2000;26:122-7.
6. Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53
modulates its effect on cell growth and apoptosis. Nature.
2000;408:377-81.
7 Boyd MT, Vlatkovic N, Haines DS. A novel cellular protein
(MTBP) binds to MDM2 and induces a G1 arrest that is
suppressed by MDM2. J Biol Chem. 2000;275(41):31883-90.
(WD0105)

13100 Kirkham Way
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www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-PERP
CATALOG No.: 2451
BACKGROUND:
The p53 tumor-suppressor gene integrates numerous
signals that control cell life and death. Several novel
molecules involved in p53 network, including Chk2 (1),
p53R2 (2), p53AIP1 (3), Noxa (4), PIDD (5), PID/MTA2 (6),
MTBP (7) and PERP (8), were identified and their genes
were cloned recently. PERP, also termed PIGPC1 and THW,
is a plasma membrane protein (8-10). p53 binds to the
promoter of PERP and transcriptionally activates PERP gene
then the translated PERP protein mediates the p53 induced
apoptosis (8). The expression of PERP causes cell death.
PERP is a mediator of p53 induced apoptosis. PERP has
sequence similarity to PMP-22/gas3 and is a new member of
the PMP-22/gas3 family (8).
SOURCE:
Rabbit anti-PERP polyclonal antibody was raised against a
synthetic peptide (EDDLLGNAKPRYFYTSA) corresponding
to amino acids 175 to 193 of human PERP, which differ from
the mouse sequence by three amino acids (7-9).
APPLICATION:
This antibody can be used for detection of PERP by Western
blot at 0.5 to 1 µg/ml. A431 cell lysate can be used as
positive control and a 21 kDa band can be detected. For
research use only.
STORAGE:
It is supplied as purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for one
year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2451P).
A431 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1202).
Western blot analysis of
PERP expression in A431
whole cell lysates in the
absence (A) and presence (B)
of blocking peptide with anti-
PERP at 1 µg /ml.
REFERENCES:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle
regulation by the Chk2 protein kinase. Science. 1998;282:1893-7.
2. Tanaka H, Arakawa H, Yamaguchi T, et al. A ribonucleotide
reductase gene involved in a p53-dependent cell-cycle checkpoint
for DNA damage. Nature. 2000;404:42-9.
3. Oda E, Ohki R, Murasawa H, et al. Noxa, a BH3-only member of
the Bcl-2 family and candidate mediator of p53-induced apoptosis.
Science. 2000;288(5468):1053-8.
4. Oda K, Arakawa H, Tanaka T, et al. p53AIP1, a potential
mediator of p53-dependent apoptosis, and its regulation by Ser-46-
phosphorylated p53. Cell. 2000 Sep 15;102(6):849-62.
5. Lin Y, Ma W, Benchimol S. Pidd, a new death-domaincontaining
protein, is induced by p53 and promotes apoptosis. Nat
Genet. 2000;26:122-7.
6. Luo J, Su F, Chen D, et al. Deacetylation of p53 modulates its
effect on cell growth and apoptosis. Nature. 2000;408:377-81.
7 Boyd MT, Vlatkovic N, Haines DS. A novel cellular protein
(MTBP) binds to MDM2 and induces a G1 arrest that is
suppressed by MDM2. J Biol Chem. 2000;275(41):31883-90.
8. Attardi,L.D., Reczek,E.E., Cosmas,C., et al. PERP, an
apoptosis-associated target of p53, is a novel member of the PMP-
22/gas3 family. Genes Dev. 2000;14 (6):704-718
9. Goltsov,A.A., Ren,C., Wang,J., et al. p53 regulates the
expression of a novel four transmembrane protein-PERP/PIGPC1
in mouse and human prostate cancer. GeneBank database
10. Hildebrandt,T., Weidle,U., Preiherr,J. et al. Identification of
THW, a putative new tumor suppressor gene. GeneBank database
(WD0105)

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Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
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Anti-IL-21 (IN)
CATALOG No.: 2465
BACKGROUND:
A novel cytokine was recently identified in human and mouse
and designated IL-21 (1), which has significant homology to
IL-2, IL-4, and IL-15. The receptor for IL-21 (IL-21R, also
termed NILR for novel Interleukin receptor) is a new member
of the class I cytokine receptor family (1,2). IL-21R forms a
complex with the common cytokine receptor γ chain, γ c , and
mediates IL-21 signaling (3,4). IL-21 and its receptor activate
JAK-STAT signaling pathway. IL-21 is expressed in activated
T cells, and HL-60 and THP-1 cell lines. IL-21 plays a role in
the proliferation and maturation of NK, B and T cell
populations.
SOURCE:
Rabbit anti-IL-21 polyclonal antibody was raised against a
synthetic peptide (TCPSCDSYEKKPPKE) corresponding to
amino acids 121 to 135 of human IL-21 precursor (1).
APPLICATION:
This antibody can be used for detection of IL-21 by Western
blot at 0.5 to 1 µg/ml. Human HL-60 and THP-1 cell lysates
can be used as positive control and an approximately 18 kDa
band can be detected.
For research use only.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2465P).
Human HL-60 cell lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1209).
Western blot analysis of IL-21
expression in HL-60 cell lysate in
the absence (lane A) or presence
of blocking peptide (lane B) with
anti-IL-21 (IN) at 1 µg /ml.
REFERENCES:
1. Parrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and
its receptor are involved in NK cell expansion and regulation of
lymphocyte function. Nature. 2000;408(6808):57-63.
2. Ozaki K, Kikly K, Michalovich D, et al. Cloning of a type I
cytokine receptor most related to the IL-2 receptor beta chain. Proc
Natl Acad Sci USA. 2000;97(21):11439-44.
3. Asao H, Okuyama C, Kumaki S, et al. the common gammachain
is an indispensable subunit of the IL-21 receptor complex. J
Immunol. 2001;167(1):1-5.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
4. Vosshenrich CA, Di Santo JP. Cytokines: IL-21 joins the
gamma(c)-dependent network? Curr Biol. 2001;11(5):R175-7.
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
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Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IL-21R (ED)
CATALOG No.: 2469
BACKGROUND:
A novel cytokine related to IL-2 and IL-15 was recently
identified and designated IL-21 (1). The receptor for IL-21
(IL-21R, also termed NILR for novel Interleukin receptor) is a
new member of the class I cytokine receptor family (1,2). IL-
21R forms a complex with the common cytokine receptor γ
chain, γ c , and mediates IL-21 signaling (3,4). Both IL-21R
and the γ c are necessary for the IL-21 function. IL-21 and its
receptor activate JAK-STAT signaling pathway. IL-21R is
expressed in spleen, thymus, natural killer (NK), T and B cell
lines. IL-21 plays a role in the proliferation and maturation of
NK, B and T cell populations.
SOURCE:
Rabbit anti-IL-21R polyclonal antibody was raised against a
synthetic peptide (NITDQSGNYSQECGS) corresponding to
amino acids 97 to 111 of human IL-21R precursor (1).
APPLICATION:
This antibody can be used for detection of IL-21R by
Western blot at 0.5 to 1 µg/ml. Human Raji and A431 cell
lysates can be used as positive control and an approximately
60 kDa band can be detected.
For research use only.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2469P).
Human Raji cell lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1207).
Western blot analysis of IL-21R
expression in human Raji cell
lysate with anti-IL-21R (ED) at 1
µg /ml.
REFERENCES:
1. Parrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and
its receptor are involved in NK cell expansion and regulation of
lymphocyte function. Nature. 2000;408(6808):57-63.
2. Ozaki K, Kikly K, Michalovich D, et al. Cloning of a type I
cytokine receptor most related to the IL-2 receptor beta chain. Proc
Natl Acad Sci USA. 2000;97(21):11439-44.
3. Asao H, Okuyama C, Kumaki S, et al. the common gammachain
is an indispensable subunit of the IL-21 receptor complex. J
Immunol. 2001;167(1):1-5.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
4. Vosshenrich CA, Di Santo JP. Cytokines: IL-21 joins the
gamma(c)-dependent network? Curr Biol. 2001;11(5):R175-7.
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IL-21R (NT)
CATALOG No.: 2471
BACKGROUND:
A novel cytokine related to IL2 and IL15 was recently
identified and designated IL-21 (1). The receptor for IL-21
(IL-21R, also termed NILR for novel Interleukin receptor) is a
new member of the class I cytokine receptor family (1,2). IL-
21R forms a complex with the common cytokine receptor γ
chain, γ c , and mediates IL-21 signaling (3,4). Both IL-21R
and the γ c are necessary for the IL-21 function. IL-21 and its
receptor activate JAK-STAT signaling pathway. IL-21R is
expressed in spleen, thymus, natural killer (NK), T and B cell
lines. IL-21 plays a role in the proliferation and maturation of
NK, B and T cell populations.
SOURCE:
Rabbit anti-IL-21R polyclonal antibody was raised against a
synthetic peptide (CPDLVCYTDYLQT) corresponding to
amino acids 20 to 32 of human IL-21R precursor (1).
APPLICATION:
This antibody can be used for detection of IL-21R by
Western blot at 0.5 to 1 µg/ml. Human Raji and A431 cell
lysates can be used as positive control and an approximately
60 kDa band can be detected.
For research use only.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2471P).
Human Raji cell lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1207).
Western blot analysis of IL-
21R expression in human Raji
cell lysate with anti-IL-21R
(NT) at 1 µg /ml.
REFERENCES:
1. Parrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and
its receptor are involved in NK cell expansion and regulation of
lymphocyte function. Nature. 2000;408(6808):57-63.
2. Ozaki K, Kikly K, Michalovich D, et al. Cloning of a type I
cytokine receptor most related to the IL-2 receptor beta chain. Proc
Natl Acad Sci USA. 2000;97(21):11439-44.
3. Asao H, Okuyama C, Kumaki S, et al. the common gammachain
is an indispensable subunit of the IL-21 receptor complex. J
Immunol. 2001;167(1):1-5.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
4. Vosshenrich CA, Di Santo JP. Cytokines: IL-21 joins the
gamma(c)-dependent network? Curr Biol. 2001;11(5):R175-7.
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-TCCR (NT)
CATALOG No.: 2481
BACKGROUND:
Upon antigen challenge, T-helper cells differentiate into two
functional distinct subsets, Th1 and Th2. Th1 cells produce
IL-2, IFN-γ and lymphotoxin-β that augment cell mediated
immune response while Th2 cells secrete IL-4, IL-5, and IL-
10 that enhance humoral immunity. The function of T-helper
cells is regulated by cytokines. A novel cytokine receptor
was recently identified and cloned (1,2). It is a new member
in the type I cytokine receptor family and designated TCCR
for T-cell cytokine receptor and WSX-1 (1,2). TCCR
deficient mice had impaired Th1 responses to protein
antigen challenge, including decreased levels of IFN-γ and
Th1-dependent antibody IgG2a (1). TCCR is predominately
expressed in thymus, spleen, lymph notes and peripheral
blood leukocytes.
SOURCE:
Rabbit anti-TCCR polyclonal antibody was raised against a
synthetic peptide (GSAGPLQCYGVGPLGD)
corresponding to amino acids 44 to 59 of human TCCR
precursor (1),
APPLICATION:
This antibody can be used for detection of TCCR by Western
blot at 0.5 to 1 µg/ml. Human spleen tissue lysate can be
used as positive control and an approximately 70 kDa band
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of
TCCR expression in human
spleen tissue lysates with
anti-TCCR at 1 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2481P).
K562 cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1306).
REFERENCES:
1. Chen Q, Ghilardi N, Wang H, Baker T, Xie MH, Gurney A,
Grewal IS and de Sauvage FJ. Development of Th1-type immune
responses requires the type I cytokine receptor TCCR Nature
2000;407(6806):916-920
2. Sprecher,C.A., Grant,F.J., Baumgartner,J.W., Presnell,S.R.,
Schrader,S.K., Yamagiwa,T., Whitmore,T.E., O'Hara,P.J. and
Foster,D.F. Cloning and characterization of a novel class I cytokine
receptor Biochem. Biophys. Res. Commun. 1998;246(1):82-90
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-TCCR (CT)
CATALOG No.: 2483
BACKGROUND:
Upon antigen challenge, T-helper cells differentiate into two
functional distinct subsets, Th1 and Th2. Th1 cells produce
IL-2, IFN-γ and lymphotoxin-β that augment cell mediated
immune response while Th2 cells secrete IL-4, IL-5, and IL-
10 that enhance humoral immunity. The function of T-helper
cells is regulated by cytokines. A novel cytokine receptor
was recently identified and cloned (1,2). It is a new member
in the type I cytokine receptor family and designated TCCR
for T-cell cytokine receptor and WSX-1 (1,2). TCCR
deficient mice had impaired Th1 responses to protein
antigen challenge, including decreased levels of IFN-γ and
Th1-dependent antibody IgG2a (1). TCCR is predominately
expressed in thymus, spleen, lymph notes and peripheral
blood leukocytes.
SOURCE:
Rabbit anti-TCCR polyclonal antibody was raised against a
synthetic peptide (SGYEKHFLPTPEELG) corresponding to
amino acids 611 to 625 of human TCCR precursor (1). This
sequence is identical to that of mouse TCCR (1,2)
APPLICATION:
This antibody can be used for detection of TCCR by Western
blot at 0.5 to 1 µg/ml. Human spleen tissue lysate can be
used as positive control and an approximately 70 kDa band
can be detected. It is human, mouse, and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of
TCCR expression in human
spleen tissue lysate with anti-
TCCR-CT at 1 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2483P).
Human spleen tissue lysate, 200 µg at 2 mg/ml, is available
for positive control (Catalog No. 1306).
REFERENCES:
1. Chen Q, Ghilardi N, Wang H, Baker T, Xie MH, Gurney A,
Grewal IS and de Sauvage FJ. Development of Th1-type immune
responses requires the type I cytokine receptor TCCR Nature
2000;407(6806):916-920
2. Sprecher,C.A., Grant,F.J., Baumgartner,J.W., Presnell,S.R.,
Schrader,S.K., Yamagiwa,T., Whitmore,T.E., O'Hara,P.J. and
Foster,D.F. Cloning and characterization of a novel class I cytokine
receptor Biochem. Biophys. Res. Commun. 1998;246(1):82-90
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IL-22R (CT)
CATALOG No.: 2489
BACKGROUND:
A novel cytokine, designated IL-TIF for IL-10 related T cellderived
inducible factor and IL-22, was recently identified (1-
3). The receptor for IL-22 (IL-22R, also termed CRF2-9 and
IL-TIF-R1 chain) is a new member of the class II cytokine
receptor family (3,4). IL-22R forms a complex with IL-10
receptor β chain and mediates IL-22 signaling. IL-22 and its
receptor activate JAK-STAT signaling pathway. IL22R is
expressed in normal liver and kidney and their cell lines
HepG2 and TK-10. A soluble form of IL-22 receptor, also
termed IL-22 binding protein (IL-22BP) and IL-22 receptor-α
2 (IL-22RA2), was identified very recently (5-7). IL-22BP
prevents binding of IL-22 to the functional cell surface IL-22R
complex and neutralizes IL-22 activity. LPS induces IL-22
expression, which indicates the role of IL-22 in inflammatory
response.
SOURCE:
Rabbit anti-IL-22R polyclonal antibody was raised against a
synthetic peptide (DSLFRGLALTVQWES) corresponding to
amino acids 560 to 574 of human IL-22R precursor (1).
APPLICATION:
This antibody can be used for detection of IL-22R by
Western blot at 0.5 to 1 µg/ml. Human HepG2 cell lysate can
be used as positive control and an approximately 62 kDa
band can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2489P). Human HepG2
cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1211).
Western blot analysis of IL-
22R expression in human
HepG2 cell lysate with anti-
IL-22R (CT) at 1 µg /ml.
REFERENCES:
1. Dumoutier L, Louahed J, Renauld JC. Cloning and
characterization of IL-10-related T cell-derived inducible factor (IL-
TIF), a novel cytokine structurally related to IL-10 and inducible by
IL-9. J Immunol. 2000;164(4):1814-9.
2. Dumoutier L, Van Roost E, Colau D, Renauld JC. Human
interleukin-10-related T cell-derived inducible factor: molecular
cloning and functional characterization as an hepatocytestimulating
factor. Proc Natl Acad Sci USA. 2000 ;97(18):10144-9.
3. Xie MH, Aggarwal S, Ho WH, et al. Interleukin (IL)-22, a novel
human cytokine that signals through the interferon receptor-related
proteins CRF2-4 and IL-22R. J Biol Chem. 2000;275(40):31335-9.
4. Kotenko SV, Izotova LS, Mirochnitchenko OV, et al.
Identification of the functional interleukin-22 (IL-22) receptor
complex: J Biol Chem. 2001;276(4):2725-32.
5. Kotenko SV, Izotova LS, Mirochnitchenko OV, et al.
Identification, cloning, and characterization of a novel soluble
receptor that binds IL-22 and neutralizes its activity. J Immunol.
2001;166(12):7096-103.
6. Dumoutier L, Lejeune D, Colau D, Renauld JC. Cloning and
characterization of il-22 binding protein, a natural antagonist of il-
10-related t cell-derived inducible factor/il-22. J Immunol.
2001;166(12):7090-5.
7. Xu W, Presnell SR, Parrish-Novak J, et al. A soluble class II
cytokine receptor, IL-22RA2, is a naturally occurring IL-22
antagonist. Proc Natl Acad Sci USA. 2001 in press (WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-IL-22R (NT)
CATALOG No.: 2497
BACKGROUND:
A novel cytokine, designated IL-TIF for IL-10 related T cellderived
inducible factor and IL-22, was recently identified (1-
3). The receptor for IL-22 (IL-22R, also termed CRF2-9 and
IL-TIF-R1 chain) is a new member of the class II cytokine
receptor family (3,4). IL-22R forms a complex with IL-10
receptor β chain and mediates IL-22 signaling. IL-22 and its
receptor activate JAK-STAT signaling pathway. IL22R is
expressed in normal liver and kidney and their cell lines
HepG2 and TK-10. A soluble form of IL-22 receptor, also
termed IL-22 binding protein (IL-22BP) and IL-22 receptor-α
2 (IL-22RA2), was identified very recently (5-7). IL-22BP
prevents binding of IL-22 to the functional cell surface IL-22R
complex and neutralizes IL-22 activity. LPS induces IL-22
expression, which indicates the role of IL-22 in inflammatory
response.
SOURCE:
Rabbit anti-IL-22R polyclonal antibody was raised against a
synthetic peptide (QSSNFENILTWDSGPE) corresponding to
amino acids 31 to 46 of human IL-22R precursor (1).
APPLICATION:
This antibody can be used for detection of IL-22R by
Western blot at 0.5 to 1 µg/ml. Human HepG2 cell lysate can
be used as positive control and an approximately 62 kDa
band can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2497P). Human HepG2
cell lysate, 200 µg at 2 mg/ml, is available for positive
control (Catalog No. 1211).
Western blot analysis of IL-22R
expression in human HepG2 cell
lysate with anti-IL-22R (NT) at 1
µg /ml.
REFERENCES:
1. Dumoutier L, Louahed J, Renauld JC. Cloning and
characterization of IL-10-related T cell-derived inducible factor (IL-
TIF), a novel cytokine structurally related to IL-10 and inducible by
IL-9. J Immunol. 2000;164(4):1814-9.
2. Dumoutier L, Van Roost E, Colau D, Renauld JC. Human
interleukin-10-related T cell-derived inducible factor: molecular
cloning and functional characterization as an hepatocytestimulating
factor. Proc Natl Acad Sci USA. 2000 ;97(18):10144-9.
3. Xie MH, Aggarwal S, Ho WH, et al. Interleukin (IL)-22, a novel
human cytokine that signals through the interferon receptor-related
proteins CRF2-4 and IL-22R. J Biol Chem. 2000;275(40):31335-9.
4. Kotenko SV, Izotova LS, Mirochnitchenko OV, et al.
Identification of the functional interleukin-22 (IL-22) receptor
complex: J Biol Chem. 2001;276(4):2725-32.
5. Kotenko SV, Izotova LS, Mirochnitchenko OV, et al.
Identification, cloning, and characterization of a novel soluble
receptor that binds IL-22 and neutralizes its activity. J Immunol.
2001;166(12):7096-103.
6. Dumoutier L, Lejeune D, Colau D, Renauld JC. Cloning and
characterization of il-22 binding protein, a natural antagonist of il-
10-related t cell-derived inducible factor/il-22. J Immunol.
2001;166(12):7090-5.
7. Xu W, Presnell SR, Parrish-Novak J, et al. A soluble class II
cytokine receptor, IL-22RA2, is a naturally occurring IL-22
antagonist. Proc Natl Acad Sci USA. 2001 in press (WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-Act1 / CIKS (CT)
CATALOG No.: 2499
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli. NF-κB associates with IκB
proteins in the cell cytoplasm, which inhibit NF-κB activity.
IκB is phosphorylated by IκB kinase (IKK) complex that
contains IKKα, IKKβ, and IKKγ. A novel molecule that
associates with and activates IKK was recently identified and
designated CIKS (for connection to IKK and SAPK/JNK) and
Act1 (for NF-κB activator 1) (1,2). CIKS directly interacts with
IKKγ. CIKS/Act1 also activates activating transcription factor
(ATF) and activator protein 1 (AP-1) through Jun kinase
(JNK). These results indicate that CIKS/Act1 is involved in
the inflammation and stress responses. CIKS/Act1 is
ubiquitously expressed in human tissues.
SOURCE:
Rabbit anti-CIKS polyclonal antibody was raised against a
synthetic peptide (REEEYVAPPRGPLPT) corresponding to
amino acids 554 to 568 of human CIKS (1,2).
APPLICATION:
This antibody can be used for detection of CIKS by Western
blot at 0.5 to 1 µg/ml. Human placenta tissue lysate can be
used as a positive control. A band at approximately 63 kDa
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of CIKS
expression in human placenta
tissue lysate with anti-CIKS (CT)
at 1 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2499P).
Human placenta tissue lysate, 200 µg at 2 mg/ml, is
available for positive control (Catalog No. 1309).
REFERENCES:
1. Leonardi A, Chariot A, Claudio E, Cunningham K, Siebenlist U.
CIKS, a connection to Ikappa B kinase and stress-activated protein
kinase. Proc Natl Acad Sci USA. 2000;97(19):10494-9.
2. Li X, Commane M, Nie H, Hua X, Chatterjee-Kishore M, Wald D,
Haag M, Stark GR. Act1, an NF-kappa B activating protein. Proc
Natl Acad Sci USA. 2000;97(19):10489-93.
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-Act1 / CIKS (NT)
CATALOG No.: 2501
BACKGROUND:
Nuclear factor kappa B (NF-κB) is a ubiquitous transcription
factor and an essential mediator of gene expression during
activation of immune and inflammatory responses. NF-κB
mediates the expression of a great variety of genes in
response to extracellular stimuli. NF-κB associates with IκB
proteins in the cell cytoplasm, which inhibit NF-κB activity.
IκB is phosphorylated by IκB kinase (IKK) complex that
contains IKKα, IKKβ, and IKKγ. A novel molecule that
associates with and activates IKK was recently identified and
designated CIKS (for connection to IKK and SAPK/JNK) and
Act1 (for NF-κB activator 1) (1,2). CIKS directly interacts with
IKKγ. CIKS/Act1 also activates activating transcription factor
(ATF) and activator protein 1 (AP-1) through Jun kinase
(JNK). These results indicate that CIKS/Act1 is involved in
the inflammation and stress responses. CIKS/Act1 is
ubiquitously expressed in human tissues.
SOURCE:
Rabbit anti-CIKS polyclonal antibody was raised against a
synthetic peptide (PPQLQETRMNRSIP) corresponding to
amino acids 2 to 15 of human CIKS (1,2).
APPLICATION:
This antibody can be used for detection of CIKS by Western
blot at 0.5 to 1 µg/ml. Human placenta tissue lysate can be
used as a positive control. A band at approximately 63 kDa
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200
µl of PBS containing 0.02% sodium azide. Store at 4°C,
stable for one year.
Western blot analysis of
CIKS expression in human
lung (lane A) and placenta
(lane B) tissue lysates with
anti-CIKS (NT) at 1 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2501P).
Human placenta tissue lysate, 200 µg at 2 mg/ml, is
available for positive control (Catalog No. 1309).
REFERENCES:
1. Leonardi A, Chariot A, Claudio E, Cunningham K, Siebenlist U.
CIKS, a connection to Ikappa B kinase and stress-activated protein
kinase. Proc Natl Acad Sci USA. 2000;97(19):10494-9.
2. Li X, Commane M, Nie H, Hua X, Chatterjee-Kishore M, Wald D,
Haag M, Stark GR. Act1, an NF-kappa B activating protein. Proc
Natl Acad Sci USA. 2000;97(19):10489-93.
(WD0108)

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-Livin, KIAP
CATALOG No.: 2505
BACKGROUND:
Apoptosis, or programmed cell death, is related to many
diseases, such as cancer. Apoptosis is triggered by a variety
of stimuli including members in the TNF family and
prevented by the inhibitor of apoptosis (IAP) proteins. IAP
proteins form a conserved gene family that binds to and
inhibits cell death proteases. A novel member in the IAP
protein family was recently identified and designated Livin
and KIAP for kidney IAP (1,2). Livin/XIAP contains a single
baculoviral IAP repeat (BIR) domain and a RING finger
domain and has two isoforms termed Livin-α and Livin-β
(1,3). Transfection of Livin in cells resulted in protection from
apoptosis induced by FADD, BAX, RIP, RIP3 and DR6 (1).
Livin has direct interaction with several caspases including
caspase-3, -7, and –9. Livin inhibits the activation of
caspase-9 induced by Apaf-1, cytochrome c, and dATP. The
two isoforms of Livin ???????to ?????different function
and tissue distribution.
SOURCE:
Rabbit anti-Livin polyclonal antibody was raised with a
synthetic peptide (CRAPVRSRVRTFLS) corresponding to
amino acids 264 to 280 of the short form and 281 to 298 of
the long form of human Livin (1,3). This sequence is identical
between α and β ????s ?? the Livin ????????.
APPLICATION:
This antibody can be used for detection of Livin by Western
blot at 2 to 4 µg/ml. Human Raji cell lysate can be used as a
positive control and a band at 33 kDa can be detected. A
lower but much weaker band at 30 kDa was detected in Raji
cell lysate, which may represent the short
??????????????
For research use only.
Western blot analysis of Livin
expression in human Raji cell lysate with
anti-Livin at 4 µg/ml.
STORAGE: It is supplied as immunoaffinity
chromatography purified IgG, 100 µg in 200 µl of PBS
containing 0.02% sodium azide. Store at 4°C, stable for
one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2505P).
Human Raji cell lysate (Catalog No. 1207), 200 µg at 2
mg/ml, is available for positive control.
REFERENCES:
1. Kasof GM, Gomes BC. Livin, a novel inhibitor of apoptosis
protein family member. J Biol Chem. 2001;276(5):3238-46.
2. Lin JH, Deng G, Huang Q, Morser J. KIAP, a novel member of
the inhibitor of apoptosis protein family. Biochem Biophys Res
Commun. 2000;279(3):820-31.
3. Ashhab Y, Alian A, Polliack A, Panet A, Yehuda DB.
Two splicing variants of a new inhibitor of apoptosis gene with
different biological properties and tissue distribution pattern.
FEBS Lett. 2001;495(1-2):56-60.
(WD0204)

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Anti-CARD9
CATALOG No.: 2515
BACKGROUND:
Apoptosis is related to many diseases and development.
Cell death signals are transduced by death domain (DD),
death effector domain (DED), and caspase recruitment
domain (CARD) containing molecules. CARD containing
proteins include some caspases, Apaf-1, CARD4, IAPs,
RICK, ARC, RAIDD, BCL-10, and ASC. A novel CARDcontaining
protein was recently identified and designated
CARD9, which interacts with the CARD activation domain of
BCL-10 (1). CARD9 associates with BCL-10 and forms a
complex within cells. CARD9 induces apoptosis and
activates NF-κB. CARD9 is an upstream activator of BCL-10
and NF-κB signaling.
SOURCE:
Rabbit anti-CARD9 polyclonal antibody was raised against a
synthetic peptide (DRENTTGSDNTDTEGS) corresponding to
amino acids 521 to 536 of human CARD9 (1). The
sequence is different from that of rat origin by two amino
acids (1).
APPLICATION:
This antibody can be used for detection of CARD9 by
Western blot at 0.5 to 1 µg/ml. Human PC-3 and MDA-MB-
361 cell lysates can be used as a positive control and a band
at approximately 59 kDa can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity purified IgG, 100 µg in 200 µl
of PBS containing 0.02% sodium azide. Store at 4°C, stable
for one year.
Western blot analysis of CARD9
expression in human MDA-MB-361
(A) and PC-3 (B) cell lysate with anti-
CARD9 at 2.5 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 2515P).
Human PC-3 lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1216).
REFERENCES:
1. Bertin J, Guo Y, Wang L, Srinivasula SM, Jacobson MD, Poyet JL,
Merriam S, Du MQ, Dyer MJ, Robison KE, DiStefano PS, Alnemri ES.
CARD9 is a novel caspase recruitment domain-containing protein that
interacts with BCL10/CLAP and activates NF-kappa B. J Biol Chem.
2000;275(52):41082-6.
(RD0202)

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Anti-ILP-2
CATALOG No.: 3017
BACKGROUND:
Apoptosis, or programmed cell death, is related to many
diseases, such as cancer. Apoptosis is triggered by a variety
of stimuli including members in the TNF family and
prevented by the inhibitor of apoptosis (IAP) proteins. IAP
proteins form a conserved gene family including IAP,
XIAP/ILP-1/MIHA, and Livin/KIAP that bind to and inhibits
specific proteases. A novel member in the IAP protein family
was recently identified and designated ILP-2 for IAP-like
protein-2 (1). ILP-2 has high homology to ILP-1, but is
encoded by a distinct gene that is solely expressed in testis
of tested normal human tissues (1). ILP-2, unlike ILP-1, has
no inhibitory effect on Fas and TNF induced apoptosis, but
potently inhibits apoptosis induced by overexpression of Bax
or by coexpression of caspase-9 with Apaf-1. ILP-2 interacts
with the processed caspase-9. These results suggest that
ILP-2 is a novel IAP family member with restricted specificity
for caspase-9.
SOURCE:
Rabbit anti-ILP-2 polyclonal antibody was raised with a
synthetic peptide (TGYEARLITFGT) corresponding to amino
acids 2 to 13 of human ILP-2 (1).
APPLICATION:
This antibody can be used for detection of ILP-2 by Western
blot at 1 to 2 µg/ml. Human HepG2 or MOLT4 cell lysate
can be used as a positive control and a band at
approximately 33 kDa can be detected. It is human, mouse,
and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of ILP-2
expression in human HepG2 (lane 1)
and MOLT4 (lane 2) cell lysates and
mouse spleen (lane 3) tissue lysates
with anti-ILP-2 at 1 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3017P).
Human HepG2 cell lysate (Catalog No. 1211), 200 µg at 2
mg/ml, is available for positive control.
REFERENCES:
1. Richter BW, Mir SS, Eiben LJ, Lewis J, Reffey SB, Frattini A, Tian
L, Frank S, Youle RJ, Nelson DL, Notarangelo LD, Vezzoni P,
Fearnhead HO, Duckett CS. Molecular cloning of ILP-2, a novel
member of the inhibitor of apoptosis protein family. Mol Cell Biol.
2001;21(13):4292-301.
(WD0204)

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Anti-ARTS
CATALOG No.: 3025
BACKGROUND:
Apoptosis is related to many diseases and development.
Mitochondrial proteins, such as cytochrome c, Apaf-1, and
AIF play important role in apoptosis. A novel mitochondrial
septin-like protein was identified recently and designated
ARTS for apoptosis related protein in TGF-β signaling
pathway (1). ARTS that is encoded by the human septin
H5/PNUTL2/CDCrel2b gene (1-4) is located to mitochondria
and translocates to the nucleus when apoptosis occurs.
ARTS is expressed in many tissues. It enhances cell death
induced by TGF-β and, to a lesser extent, by other apoptotic
agents, such as TNF-α and Fas ligand.
SOURCE:
Rabbit anti-ARTS polyclonal antibody was raised against a
synthetic peptide (KRFLEDTTDDGE) corresponding to
amino acids 3 to 14 of human ARTS (1).
APPLICATION:
This antibody can be used for detection of ARTS by Western
blot at 0.5 to 2 µg/ml. Human lung, kidney and spleen tissue
lysates can be used as a positive control and a band at 32
kDa can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3025P).
Human lung tissue lysate, 200 µg at 2 mg/ml, is available for
positive control (Catalog No. 1302).
Western blot analysis of ARTS
expression in human lung (lane 1),
spleen (lane 2), and kidney (lane 3)
tissue lysates with anti-ARTS at 2 µg /ml.
REFERENCES:
1. Larisch S, Yi Y, Lotan R, Kerner H, et al. A novel mitochondrial
septin-like protein, ARTS, mediates apoptosis dependent on its P-
loop motif. Nat Cell Biol 2000;2(12):915-21
2. Depraetere V. The ARTS of apoptosis. Nat Cell Biol.
2000;2(12):E219.
3. Paavola,P., Horelli-Kuitunen,N., Palotie,A. and Peltonen,L.
Characterization of a novel gene, PNUTL2, on human chromosome
17q22-q23 and its exclusion as the Meckel syndrome gene.
Genomics 1999;55 (1):122-125
4. Zieger,B., Tran,H., Hainmann,I., Wunderle,D., Zgaga-Griesz,A.,
Blaser,S. and Ware,J. Characterization and expression analysis of
two human septin genes, PNUTL1 and PNUTL2. Gene
2000;261(2):197-203
(WD0204)

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Toll Free: 888-513-9525
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Fax: 858-513-2692
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Anti-Bmf (CT)
CATALOG No.: 3029
BACKGROUND:
Apoptosis is related to many diseases and development.
Members in the Bcl-2 family are critical regulators of
apoptosis by either inhibiting or promoting cell death. Bcl-2
homology 3 (BH3) domain is a potent death domain. BH3-
only proteins, including Bad, Bid, Bik, Hrk, Bim, Noxa, and
PUMA, form a growing subclass of the Bcl-2 family. A novel
BH3-only protein was recently identified in human and
mouse and designated Bmf (for Bcl-2-modifing factor) (1).
The BH3 domain in Bmf is required both for binding to Bcl-2
proteins and for triggering apoptosis. In healthy cells, Bmf
associates with the dynein light chain 2 (DLC2) component
of the myosin V motors and is sequestered by the cell’s actin
cytoskeleton. Disruption of the actin cytoskeleton, either by
depolymerization of actin filaments or by detachment of cells
from the extracellular matrix, triggers release and activation
of Bmf, initiating the downstream apoptotic program (1,2).
Bmf is constitutively expressed in many tissues (1,2).
SOURCE:
Rabbit anti-Bmf polyclonal antibody was raised with a
synthetic peptide (ALNGEENRNGAGPR) corresponding to
amino acids 171 to 184 of human Bmf (1).
APPLICATION:
This antibody can be used for detection of Bmf by Western
blot at 2 µg/ml. HepG2 or 293 cell lysate can be used as a
positive control and a band at approximately 25 kDa can be
detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3029P).
HepG2 (Catalog No. 1204) cell lysate, 200 µg at 2 mg/ml, is
available for positive control
REFERENCES:
1. Puthalakath H, Villunger A, O'Reilly LA, Beaumont JG, Coultas L,
Cheney RE, Huang DC, Strasser A. Bmf: a proapoptotic BH3-only
protein regulated by interaction with the myosin V actin motor
complex, activated by anoikis.
Science. 2001;293(5536):1829-32.
2. Hunt A, Evan G. Apoptosis. Till death us do part. Science.
2001;293(5536):1784-5.
(WD0204)

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www.prosci-inc.com
Toll Free: 888-513-9525
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Fax: 858-513-2692
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Anti-Bmf (NT)
CATALOG No.: 3031
BACKGROUND:
Apoptosis is related to many diseases and development.
Members in the Bcl-2 family are critical regulators of
apoptosis by either inhibiting or promoting cell death. Bcl-2
homology 3 (BH3) domain is a potent death domain. BH3-
only proteins, including Bad, Bid, Bik, Hrk, Bim, Noxa, and
PUMA, form a growing subclass of the Bcl-2 family. A novel
BH3-only protein was recently identified in human and
mouse and designated Bmf (for Bcl-2-modifing factor) (1).
The BH3 domain in Bmf is required both for binding to Bcl-2
proteins and for triggering apoptosis. In healthy cells, Bmf
associates with the dynein light chain 2 (DLC2) component
of the myosin V motors and is sequestered by the cell’s actin
cytoskeleton. Disruption of the actin cytoskeleton, either by
depolymerization of actin filaments or by detachment of cells
from the extracellular matrix, triggers release and activation
of Bmf, initiating the downstream apoptotic program (1,2).
Bmf is constitutively expressed in many tissues (1,2).
SOURCE:
Rabbit anti-Bmf polyclonal antibody was raised with a
synthetic peptide (EPSQCVEELEDDV) corresponding to
amino acids 2 to 14 of human Bmf (1). This sequence differs
from that of mouse by one amino acid.
APPLICATION:
This antibody can be used for detection of Bmf by Western
blot at 2 µg/ml. HepG2 or 293 cell lysate can be used as a
positive control and a band at approximately 25 kDa can be
detected. It is human and mouse reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of Bmf
expression in human HepG2 (lane 1)
and 293 (lane 2) cell lysates with anti-
Bmf at 2 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3031P).
HepG2 (Catalog No. 1204) cell lysate, 200 µg at 2 mg/ml, is
available for positive control
REFERENCES:
1. Puthalakath H, Villunger A, O'Reilly LA, Beaumont JG, Coultas L,
Cheney RE, Huang DC, Strasser A. Bmf: a proapoptotic BH3-only
protein regulated by interaction with the myosin V actin motor
complex, activated by anoikis.
Science. 2001;293(5536):1829-32.
2. Hunt A, Evan G. Apoptosis. Till death us do part. Science.
2001;293(5536):1784-5.
(WD0204)

13100 Kirkham Way
Suite 207
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www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-EndoG
CATALOG No.: 3035
BACKGROUND:
The fragmentation of nuclear DNA is a hallmark of apoptotic
cell death. The activities of caspase and nuclease are
involved in the DNA fragmentation. Caspase-activated
deoxyribonuclease (CAD), also termed DNA fragmentation
factor (DFF40), is one such nuclease, and is capable of
inducing DNA fragmentation and chromatin condensation
after cleavage by caspase-3 of its inhibitor ICAD/DFF45.
Caspase and CAD independent DNA fragmentation also
exists. Recent studies demonstrated that another nuclease,
endonuclease G (endoG), is specifically activated by
apoptotic stimuli and is able to induce nucleosomal
fragmentation of DNA independently of caspase and
DFF/CAD (1,2). EndoG is a mitochondrion-specific nuclease
that translocates to the nucleus and cleaves chromatin DNA
during apoptosis. The homologue of mammalian EndoG is
the first mitochondrial protein identified to be involved in
apoptosis in C. elegans (2). EndooG also cleaves DNA in
vitro (4).
SOURCE:
Rabbit anti-EndoG polyclonal antibody was raised with a
synthetic peptide (GGPRGPGELAKYGLP) corresponding to
amino acids 55 to 70 of human EndoG (5).
APPLICATION:
This polyclonal antibody can be used for detection of EndoG
by Western blot at 1 to 2 µg/ml. HepG2 and 3T3 cell lysates
can be used as positive control and a 35 kDa band can be
detected. It is human, mouse and rat reactive.
For research use only.
STORAGE:
It is supplied as affinity chromatography purified IgG, 100 µg
in 100 µl of PBS containing 0.02% sodium azide. Store at
4°C, stable for one year.
Western blot analysis of EndoG in
mouse (M) 3T3 and human (H) HepG2
cell lysates with anti-EndoG at 2 µg/ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3035P).
HepG2 cell lysate (Catalog No. 1211), 200 µg at 2 mg/ml, is
available for positive control.
REFERENCES:
1. Li LY, Luo X, Wang X. Endonuclease G is an apoptotic DNase
when released from mitochondria. Nature. 2001;412(6842):95-9.
2. Parrish J, Li L, Klotz K, Ledwich D, Wang X, Xue D. Mitochondrial
endonuclease G is important for apoptosis in C. elegans. Nature.
2001;412(6842):90-4
3. Hengartner MO. Apoptosis. DNA destroyers. Nature.
2001;412(6842):27, 29.
4. Widlak P, Li LY, Wang X, Garrard WT. Action of recombinant
human apoptotic endonuclease G on naked DNA and chromatin
substrates: cooperation with exonuclease and DNase I. J Biol
Chem. 2001;276(51):48404-9.
5. Tiranti V, Rossi E, Ruiz-Carrillo A, Rossi G, Rocchi M, DiDonato
S, Zuffardi O, Zeviani M. Chromosomal localization of mitochondrial
transcription factor A (TCF6), single-stranded DNA-binding protein
(SSBP), and endonuclease G (ENDOG), three human
housekeeping genes involved in mitochondrial biogenesis.
Genomics. 1995;25(2):559-64. (WD0204)

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Anti-PUMA (CT) bbc3
CATALOG No.: 3041
BACKGROUND:
Apoptosis is related to many diseases and development. The
p53 tumor-suppressor protein induces apoptosis through
transcriptional activation of several genes. A novel p53
inducible pro-apoptotic gene was identified recently and
designated PUMA (for p53 upregulated modulator of
apoptosis) and bbc3 (for Bcl-2 binding component 3) in
human and mouse (1-3). PUMA/bbc3 is one of the proapoptotic
Bcl-2 family members including Bax and Noxa,
which are also transcriptional targets of p53. The PUMA
gene encodes two BH3 domain-containing proteins termed
PUMA-α and PUMA-β (1). PUMA proteins bind Bcl-2,
localize to the mitochondria, and induce cytochrome c
release and apoptosis in response to p53. PUMA may be a
direct mediator of p53-induced apoptosis.
SOURCE:
Rabbit anti-PUMA polyclonal antibody was raised against a
synthetic peptide (PLPRGHRAPEMEPN) corresponding to
amino acids 180 to 193 of human PUMA-α (1). This
sequence is identical between α and β ????????the
????????????.
APPLICATION:
This antibody can be used for detection of PUMA by
Western blot at 1 to 2 µg/ml. K562 or 3T3 cell lysate can be
used as a positive control and a band at approximately 23
kDa can be detected. A lower band at approximately 16 kDa
was detected in MOLT4 and U937 cells, which may
represent the PUMA-β ????? It is human and mouse
reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of PUMA
expression in human (H) K562 and
mouse (M) 3T3 cell lysates with anti-
PUMA at 2 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3041P).
K562 (Catalog No. 1204) or 3T3 (Catalog No. 1212) cell
lysate, 200 µg at 2 mg/ml, is available for positive control
REFERENCES:
1. Nakano K, Vousden KH. PUMA, a novel proapoptotic gene, is
induced by p53. Mol Cell. 2001;7(3):683-94.
2. Yu J, Zhang L, Hwang PM, Kinzler KW, Vogelstein B. PUMA
induces the rapid apoptosis of colorectal cancer cells. Mol Cell.
2001;7(3):673-82.
3. Han J, Flemington C, Houghton AB, Gu Z, Zambetti GP, Lutz RJ,
Zhu L, Chittenden T. Expression of bbc3, a pro-apoptotic BH3-only
gene, is regulated by diverse cell death and survival signals. Proc
Natl Acad Sci U S A. 2001;98(20):11318-23.
(WD0204)

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Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
Anti-PUMA (NT) bbc3
CATALOG No.: 3043
BACKGROUND:
Apoptosis is related to many diseases and development. The
p53 tumor-suppressor protein induces apoptosis through
transcriptional activation of several genes. A novel p53
inducible pro-apoptotic gene was identified recently and
designated PUMA (for p53 upregulated modulator of
apoptosis) and bbc3 (for Bcl-2 binding component 3) in
human and mouse (1-3). PUMA/bbc3 is one of the proapoptotic
Bcl-2 family members including Bax and Noxa,
which are also transcriptional targets of p53. The PUMA
gene encodes two BH3 domain-containing proteins termed
PUMA-α and PUMA-β (1). PUMA proteins bind Bcl-2,
localize to the mitochondria, and induce cytochrome c
release and apoptosis in response to p53. PUMA may be a
direct mediator of p53-induced apoptosis.
SOURCE:
Rabbit anti-PUMA polyclonal antibody was raised with a
synthetic peptide (ARARQEGSSPEPVEG) corresponding to
amino acids 2 to 16 of human PUMA-α (1). This sequence is
identical between human and mouse PUMA.
APPLICATION:
This antibody can be used for detection of PUMA by
Western blot at 2 to 4 µg/ml. K562 cell lysate can be used
as a positive control and a band at approximately 23 kDa
can be detected.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of PUMA
expression in human K562 cell lysate
with anti-PUMA at 2 µg /ml.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3043P).
K562 cell lysate (Catalog No. 1204), 200 µg at 2 mg/ml, is
available for positive control.
REFERENCES:
1. Nakano K, Vousden KH. PUMA, a novel proapoptotic gene, is
induced by p53. Mol Cell. 2001;7(3):683-94.
2. Yu J, Zhang L, Hwang PM, Kinzler KW, Vogelstein B. PUMA
induces the rapid apoptosis of colorectal cancer cells. Mol Cell.
2001;7(3):673-82.
3. Han J, Flemington C, Houghton AB, Gu Z, Zambetti GP, Lutz RJ,
Zhu L, Chittenden T. Expression of bbc3, a pro-apoptotic BH3-only
gene, is regulated by diverse cell death and survival signals. Proc
Natl Acad Sci U S A. 2001;98(20):11318-23.
(WD0204)

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Suite 207
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Toll Free: 888-513-9525
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techsupport@prosci-inc.com
Anti-p53DINP1, SIP
CATALOG No.: 3045
BACKGROUND:
Apoptosis is related to many diseases and development. The
p53 tumor-suppressor protein induces apoptosis through
transcriptional activation of several genes. A novel p53
inducible gene was identified recently and designated
p53DINP1 (for p53-dependent damage-inducible nuclear
protein 1) and SIP (for stress induced protein) in human and
mouse (1,2). A p53DINP1 antisense oligonucleotide inhibits
and overexpression of p53DINP1 enhances Ser46
phosphorylation of p53, induction of p53AIP1, and cell death
induced by DNA double-strand breaks (1). p53DINP1 may
regulate p53-dependent apoptosis through phosphorylation
at Ser46 and induction of p53AIP1. The p53DINP1/SIP gene
encodes two proteins of 27 and 18 kDa in human and mouse
termed p53DINP1-α and p53DINP1-β or SIP 27 and SIP 18
(1,2). p53DINP1/SIP is expressed in many tissues and
induced by a variety of stress agents including UV stress,
mutagenic stress, heat shock, and oxidative stress (2).
SOURCE:
Rabbit anti-p53DINP1 polyclonal antibody was raised with a
synthetic peptide (MFQRLNKMFVGEVS) corresponding to
amino acids 1 to 14 of human p53DINP1 (1). This sequence
is identical between α and β ????????the
p53DINP1????????, and differs by one amino acid from
those of mouse.
APPLICATION:
This antibody can be used for detection of p53DINP1 by
Western blot at 1 to 2 µg/ml. Human lung tissue lysate can
be used as a positive control and a band at 27 kDa can be
detected. A lower band at 18 kDa was detected in human
spleen, and mouse liver and kidney tissue lysates, which
may represent the p53DINP1-β ????? It is human, mouse,
and rat reactive.
For research use only.
STORAGE:
It is supplied as immunoaffinity chromatography purified IgG,
100 µg in 100 µl of PBS containing 0.02% sodium azide.
Store at 4°C, stable for one year.
Western blot analysis of
p53DINP1 expression in human
lung tissue lysate with antip53DINP1
at 2 µg/ml in the
absence (lane 1) or presence
(lane 2) of blocking peptide.
RELATED PRODUCTS:
Blocking peptide, 50 µg at 200 µg/ml, is available for
competition studies (Catalog No. 3045P).
Human lung tissue lysate (Catalog No. 1302), 200 µg at 2
mg/ml, is available for positive control.
REFERENCES:
1. Okamura S, Arakawa H, Tanaka T, Nakanishi H, Ng CC, Taya Y,
Monden M, Nakamura Y. p53DINP1, a p53-inducible gene,
regulates p53-dependent apoptosis. Mol Cell. 2001;8(1):85-94.
2. Tomasini R, Samir AA, Vaccaro MI, Pebusque MJ, Dagorn JC,
Iovanna JL, Dusetti NJ. Molecular and functional characterization of
the stress-induced protein (SIP) gene and its two transcripts
generated by alternative splicing. SIP induced by stress and
promotes cell death. J Biol Chem. 2001;276(47):44185-92.
(WD0204)

peptide Data Sheets

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IRAK (CT) peptide
CATALOG NO.: 1007P
SEQUENCE: DRQGPEESDEFQS
LOCATION: Amino acids 700 to 712 of human IRAK (1)
APPLICATION:
The peptide is used for blocking the activity of anti-IRAK (CT, catalog number 1007). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
IRAK in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Cao Z; Henzel WJ; Gao X. IRAK: a kinase associated with the interleukin-1 receptor. Science
1996;271:1128-31.

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CXCR4 (NT) peptide
CATALOG NO.: 1009P
SEQUENCE: MEGISIYTSDNYTE
LOCATION: Amino acids 1 to 14 of human CXCR4 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-CXCR4 (NT, catalog number 1009). Incubating
the peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of
anti-CXCR4 (NT) in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Berson J.F. et al. J Virol 1996;70:6288-95.
2. Leoetscher M. et al. J Biol Chem 1994;269:232-237

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CXCR4 (EL) peptide
CATALOG NO.: 1012P
SEQUENCE: DRYICDRFYPNDLWV
LOCATION: Amino acids 182 to 196 of human CXCR4 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-CXCR4 (EL, catalog number 1012). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
CXCR4 (EL) in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Berson J.F. et al. J Virol 1996;70:6288-95.
2. Leoetscher M. et al. J Biol Chem 1994;269:232-237

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CCR5 (NT) peptide
CATALOG NO.: 1112P
SEQUENCE: SSPIYDINYYTSEPC
LOCATION: Amino acids 6 to 20 of human CCR5 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-CCR5 (catalog number 1112). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
CCR5 in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Raport, CJ, et al. J Biol Chem 1996;271:17161-6
2. Combadiere, C. et al. J Leuk Biol 1996;60:147-52

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TRAIL (CT) peptide
CATALOG NO.: 1113P
SEQUENCE: CTNEHLIDMDHEASFFGA
LOCATION: Amino acids 261 to 277 of human TRAIL (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-TRAIL (catalog number 1113). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
TRAIL (CT) in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Wiley SR, Schooley K, Smolak PJ, Din WS, Huang CP, Nicholl JK, Sutherland GR, Smith TD, Rauch
C, Smith CA, et al. Identification and characterization of a new member of the TNF family that
induces apoptosis. Immunity 1995;3:673-682
2. Pitti RM; Marsters SA; Ruppert S; Donahue CJ; Moore A; Ashkenazi A. Induction of apoptosis by
Apo-2 ligand, a new member of the tumor necrosis factor cytokine family. J. Biol. Chem.
1996;271:12687-90

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RAIDD (IN) peptide
CATALOG NO.: 1115P
SEQUENCE: CAGDRLTGIPSHILNSSPSD
LOCATION: Amino acids 99 to 117 of human RAIDD (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-RAIDD (catalog number 1115). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
RAIDD (IN) in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Duan H, Dixit VM. RAIDD is a new 'death' adaptor molecule. Nature 1997;385:86-89
2. Ahmad M, Srinivasula SM, Wang L, Talanian RV, Litwack G, Fernandes-Alnemri T, Alnemri ES.
CRADD, a novel human apoptotic adaptor molecule for caspase-2, and FasL/tumor necrosis factor
receptor-interacting protein RIP. Cancer Res 1997

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RAIDD (CT) peptide
CATALOG NO.: 1117P
SEQUENCE: CHNGLRAVEVDPSLLLHMLE
LOCATION: Amino acids 181 to 199 of human RAIDD (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-RAIDD (catalog number 1117). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Duan H, Dixit VM. RAIDD is a new 'death' adaptor molecule. Nature 1997;385:86-89
2. Ahmad M, Srinivasula SM, Wang L, Talanian RV, Litwack G, Fernandes-Alnemri T, Alnemri ES.
CRADD, a novel human apoptotic adaptor molecule for caspase-2, and FasL/tumor necrosis factor
receptor-interacting protein RIP. Cancer Res 1997 57:615-619

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DR3 (CT) peptide
CATALOG NO.: 1120P
SEQUENCE: ERMGLDGCVEDLRSRLQRGP
LOCATION: Amino acids 398 to 417 of human DR3 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DR3 (catalog number 1120). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan DR; Xing L; Gentz R; Ni J; Dixit
VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT; Grinham CJ; Brown R; Farrow SN.
Nature, 1996;384:372-5.

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Neurturin peptide
CATALOG NO.: 1121P
SEQUENCE: DAHSRYHTVHELSARE
LOCATION: Amino acids 178 to 193 of human neurturin (1)
APPLICATION:
The peptide is used for blocking the activity of anti-neurturin (catalog number 1121). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kotzbauer PT, Lampe PA, Heuckeroth RO, Golden JP, Creedon DJ, Johnson EM Jr, lbrandt J.
Neurturin, a relative glial-cell-line-derived neurotrophic factor. Nature 1996;384:467-470

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Eotaxin peptide
CATALOG NO.: 1123P
SEQUENCE: NH 2 -DSMKYLDQKSPTPKP-OH
LOCATION: Amino acids 83 to 97 of human eotaxin (1-2).
Application:
The peptide is used for blocking the antibody activity of eotaxin (catalog number 1123). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kitaura M, Nakajima T, Imai T, et al. Molecular cloning of human eotaxin, an eosinophil-selective
CC chemokine, and identification of a specific eosinophil eotaxin receptor, CC chemokine receptor 3. J
Biol Chem 1996;271:7725-30
2. Ponath PD, Qin S, Ringler DJ, et al. Cloning of the human eosinophil chemoattractant, eotaxin.
Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment
of eosinophils. J Clin Invest 1996;97:604-12

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SIRPα (CT) peptide
CATALOG NO.: 1125P
SEQUENCE: KPEPSFSEYASVQVPRK
LOCATION: Amino acids 487 to 503 of human SIRPα (1)
APPLICATION:
The peptide is used for blocking the activity of anti-SIRPα (catalog number 1125). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kharitonenkov A, et al. Nature 1997;386:181-186.

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Toll Free: 888-513-9525
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Caspase-10 (CT) peptide
CATALOG NO.: 1128P
SEQUENCE: ISAQTPRPPMRRWSSVS
LOCATION: Amino acids 505 to 521 of human caspase-10 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-caspase-10 (catalog number 1128). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Vincenz.C. and Dixit,V.M. Fas-associated death domain protein interleukin-1beta-converting enzyme 2 (FLICE2),
an ICE/Ced-3 homologue, is proximally involved in CD95- and p55-mediated death signaling. J. Biol. Chem.
1997;272:6578-6583

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Toll Free: 888-513-9525
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techsupport@prosci-inc.com
NIK (CT) peptide
CATALOG NO.: 1129P
SEQUENCE: SFAWSWRVKHGQLENRP
LOCATION: Amino acids 931 to 947 of human NIK (1)
APPLICATION:
The peptide is used for blocking the activity of anti-NIK (catalog number 1129). Incubating the peptide
with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity in
Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Malinin NL, Boldin MP, Kovalenko AV, Wallach . MAP3K-related kinase involved in NF-kappaB
induction by TNF, CD95 and IL-1. Nature 1997;385:540-544

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TACE (CT) peptide
CATALOG NO.: 1131P
SEQUENCE: ASFKLQRQNRVDSKETE
LOCATION: Amino acids 807 to 823 of human TACE (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-TACE (CT, catalog number 1131). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the activity of anti-
TACE in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCES:
1. Black RA, Rauch CT, Kozlosky CJ, et al. A metalloproteinase disintegrin that releases tumournecrosis
factor-alpha from cells. Nature 1997;385:729-733
2. Moss ML, Jin SL, Milla ME, et al. Cloning of a disintegrin metalloproteinase that processes precursor
tumour-necrosis factor-alpha. Nature 1997;385:733-736

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GFRα-1 (IN) peptide
CATALOG NO.: 1133P
SEQUENCE: KNKPLGPAGSENEI
LOCATION: Amino acids 369 to 382 of human GFRα-1 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-GFRα-1 (catalog number 1133). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Jing S; Wen D; Yu Y; Holst PL ; Luo Y; Fang M; Tamir R; Antonio L; Hu Z; Cupples R; Louis JC;
Hu S; Altrock BW; Fox GM. GDNF-induced activation of the Ret protein tyrosien kinase is mediated
by GDNFR-? , a novel receptor for GDNF. Cell, 1996;85:1113-24.
2. Treanor JJS; GoodmanL; Sauvage FD; Stone DM; Poulsen KT; Beck CD; Gray C; Armanini MP;
Pollock RA; Herti F; Phillips HS; Goddard A; Moore MW; Buj-Bello A;Davies AM; Asai N;
Takahashi M; Vandlen R; Henderson CE; Rosenthal A. Characterization of a multicomponent receptor
for GDNF. Nature, 1996;382:80-83.

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GFRα-3 (IN) peptide
CATALOG NO.: 1137P
SEQUENCE: RFHRQLFSQDWADS
LOCATION: Amino acids 347 to 360 of murine GFRα-3 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-GFRα-3 (catalog number 1137). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Naveilhan P, Baudet C, Mikaels A, Shen L, Westphal H, Ernfors P. Expression and regulation of
GFRalpha3, a glial cell line-derived neurotrophic factor family receptor. Proc Natl Acad Sci USA
1998;95:1295-1300.

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Toll Free: 888-513-9525
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DR4 (CT) peptide
CATALOG NO.: 1139P
SEQUENCE: CDSGKFIYLEDGTGSAVSLE
LOCATION: Amino acids 427 to 445 of human DR4 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DR4 (catalog number 1139). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R; Ebner R; Ni J; Dixit VM. The receptor
for the cytotoxic ligand TRAIL. Science; 1997;276:111-113

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DFF45 (CT) peptide
CATALOG NO.: 1141P
SEQUENCE: KASPPGDLQNPKRARQDPT
LOCATION: Amino acids 313 to 331 of human DFF45 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DFF45 (catalog number 1141). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric protein that functions downstream of
caspase-3 to trigger DNA fragmentation during apoptosis. Cell 1997;89:175-184

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DFF45/35 (NT) peptide
CATALOG NO.: 1148P
SEQUENCE: EVTGDAGVPESGEIRTLKPC
LOCATION: Amino acids 2 to 21 of human DFF45/35 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DFF45/35 (catalog number 1148). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Liu X, Zou H, Slaughter C, Wang X. DFF, a heterodimeric protein that functions downstream of
caspase-3 to trigger DNA fragmentation during apoptosis. Cell 1997;89:175-184

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Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
MADD (NT) peptide
CATALOG NO.: 1150P
SEQUENCE: AAVHSSEEDLRTPPRPVSS
LOCATION: Amino acids 1570 to 1588 of human MADD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-MADD (catalog number 1150). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Schievella AR, Chen JH, Graham JR, Lin LL. MADD, a novel death domain protein that interacts with
the type 1 tumor necrosis factor receptor and activates mitogen-activated protein kinase. J Biol Chem
1997;272:12069-12075

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mFLIP (CT) peptide
CATALOG NO.: 1156P
SEQUENCE: DKVYAWNSGVSSKEKYS
LOCATION: Amino acids 449 to 465 of human mFLIP (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-mFLIP (catalog number 1156). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V, Bodmer JL, Schroter M, Burns K,
Mattmann C, Rimoldi D, French LE, Tschopp J. Inhibition of death receptor signals by cellular FLIP.
Nature 1997;388:190-195.
2. Goltsev YV, Kovalenko AV, Arnold E, Varfolomeev EE, Brodianskii VM, Wallach D. CASH, a
novel caspase homologue with death effector domains. J Biol Chem 1997;272:19641-19644.

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DR3 (ED) peptide
CATALOG NO.: 1158P
SEQUENCE: APCTEPCGNSTCLVCPQDT
LOCATION: Amino acids 59 to 77 of human DR3 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DR3 (catalog number 1158). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan DR; Xing L; Gentz R; Ni J; Dixit
VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT; Grinham CJ; Brown R; Farrow SN.
Nature, 1996;384:372-5.

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Suite 207
Poway, CA 92064
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FLIP (NT) peptide
CATALOG NO.: 1159P
SEQUENCE: SAEVIHQVEEALDTDEKE
LOCATION: Amino acids 2 to 18 of human FLIP (1)
APPLICATION:
The peptide is used for blocking the activity of anti-FLIP (catalog number 1159). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V, Bodmer JL, Schroter M, Burns K,
Mattmann C, Rimoldi D, French LE, Tschopp J. Inhibition of death receptor signals by cellular FLIP.
Nature 1997;388:190-195

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FLIPα (CT) peptide
CATALOG NO.: 1161P
SEQUENCE: NGYMYDWNSRVSAKEKYY
LOCATION: Amino acids 447 to 464 of human FLIP? (1)
APPLICATION:
The peptide is used for blocking the activity of anti-FLIP? (catalog number 1161). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V, Bodmer JL, Schroter M, Burns K,
Mattmann C, Rimoldi D, French LE, Tschopp J. Inhibition of death receptor signals by cellular FLIP.
Nature 1997;388:190-195

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Daxx (CT) peptide
CATALOG NO.: 1163P
SEQUENCE: TSVATQCDPEEIIVLSDSD
LOCATION: Amino acids 722 to 740 of human Daxx (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-Daxx (catalog number 1163). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Yang X, Khosravi-Far R, Chang HY, Baltimore D. Daxx, a novel Fas-binding protein that activates
JNK and apoptosis. Cell 1997;89:1067-1076
2. Kiriakidou M, Driscoll DA, Lopez-Guisa JM, Strauss JF 3rd. Cloning and expression of primate Daxx
cDNAs and mapping of the human gene to chromosome 6p21.3 in the MHC region. DNA Cell Biol
1997;16:1289-1298 5.

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DR3 (NT) peptide
CATALOG NO.: 1166P
SEQUENCE: QGGTRSPRCDCAGDFH
LOCATION: Amino acids 25 to 40 of human DR3 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DR3 (catalog number 1166). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Chinnaiyan AM; O'Rourke K; Yu GL; Lyons RH; Garg M; Duan DR; Xing L; Gentz R; Ni J; Dixit
VM. Science, 1996;274:990-2.
2. Kitson J; Raven T; Jiang YP; Goeddel DV; Giles KM; Pun KT; Grinham CJ; Brown R; Farrow SN.
Nature, 1996;384:372-5.

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DR4 (NT) peptide
CATALOG NO.: 1167P
SEQUENCE: ASGTEAAAATPSKVWGSSAG
LOCATION: Amino acids 1 to 20 of human DR4 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DR4 (catalog number 1167). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R; Ebner R; Ni J; Dixit VM. The receptor
for the cytotoxic ligand TRAIL. Science; 1997;276:111-113

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Bonzo (CT) peptide
CATALOG NO.: 1170P
SEQUENCE: KSSEDNSKTFSASHNVEATS
LOCATION: Amino acids 319 to 338 of human Bonzo (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-Bonzo (catalog number 1170). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Deng HK, Unutmaz D, KewalRamani VN, Littman DR. Expression cloning of new receptors used by
simian and human immunodeficiency viruses. Nature 1997;388:296-300
2. Liao F, Alkhatib G, Peden KW, Sharma G, Berger EA, Farber JM. STRL33, A novel chemokine
receptor-like protein, functions as a fusion cofactor for both macrophage-tropic and T cell line-tropic
HIV-1. J Exp Med 1997;185:2015-23.

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ICAD (NT) peptide
CATALOG NO.: 2001P
SEQUENCE: ELSRGASAPDPDDVRPLKPC
LOCATION: Amino acids 2 to 21 of murine ICAD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ICAD (catalog number 2001). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A caspase-activated DNase that
degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50

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ICAD (CT) peptide
CATALOG NO.: 2003P
SEQUENCE: -RRSPLPGEPQRPKRAKRDSS
LOCATION: Amino acids 312 to 331 of murine ICAD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ICAD (catalog number 2003). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A caspase-activated DNase that
degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50

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CAD (I17) peptide
CATALOG NO.: 2007P
SEQUENCE: YNGSYFDRGAEASSRL
LOCATION: Amino acids 205 to 222 of murine CAD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-CAD (catalog number 2007). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A caspase-activated DNase that
degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50

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CAD (CT) peptide
CATALOG NO.: 2011P
SEQUENCE: KLECDRSRIYRPQTGS
LOCATION: Amino acids 314 to 329 of murine CAD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-CAD (catalog number 2011). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A caspase-activated DNase that
degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50

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Apaf-1 (NT) peptide
CATALOG NO.: 2013P
SEQUENCE: HREALEKDIKTSYIMDHC
LOCATION: Amino acids 12 to 28 of human Apaf-1 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-Apaf-1 (catalog number 2013). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Zou H, Henzel WJ, Liu X, Lutschg A, Wang X. Apaf-1, a human protein homologous to C. elegans
CED-4, participates in cytochrome c-dependent activation of caspase-3. Cell 1997;90:405-13

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Apaf-1 (CT) peptide
CATALOG NO.: 2015P
SEQUENCE: TFYTNGTNLKKIHVSPDFKT
LOCATION: Amino acids 1158 to 1177 of human Apaf-1 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-Apaf-1 (catalog number 2015). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Zou H, Henzel WJ, Liu X, Lutschg A, Wang X. Apaf-1, a human protein homologous to C. elegans
CED-4, participates in cytochrome c-dependent activation of caspase-3. Cell 1997;90:405-13

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DR5 (CT) peptide
CATALOG NO.: 2019P
SEQUENCE: KIEDHLLSSGKFMYLEGNAD
LOCATION: Amino acids 388 to 407 of human DR5 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DR5 (catalog number 2019). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G, Ni J, Wei YF, Yu G, Gentz R, Dixit VM. An antagonist decoy receptor and a death domaincontaining
receptor for TRAIL. Science 1997;277:815-8
2. Sheridan JP, Marsters SA, Pitti RM, Gurney A, Skubatch M, Baldwin D, Ramakrishnan L, Gray CL,
Baker K, Wood WI, Goddard AD, Godowski P, Ashkenazi A. Control of TRAIL-induced apoptosis by
a family of signaling and decoy receptors. Science 1997;277:818-21

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DcR2 (ID) peptide
CATALOG NO.: 2021P
SEQUENCE: GGPERVHRVLFRRRS
LOCATION: Amino acids 249 to 263 of human DcR2 (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-DcR2 (catalog number 2021). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G; O'Rourke K; Chinnaiyan AM; O'Rourke K; Gentz R; Ebner R; Ni J; Dixit VM. The receptor
for the cytotoxic ligand TRAIL. Science; 1997;276:111-113
2. Pan G, Ni J, Wei YF, Yu G, Gentz R, Dixit VM. An antagonist decoy receptor and a death domaincontaining
receptor for TRAIL. Science 1997;277:815-8
3. Sheridan JP, Marsters SA, Pitti RM, Gurney A, Skubatch M, Baldwin D, Ramakrishnan L, Gray CL,
Baker K, Wood WI, Goddard AD, Godowski P, Ashkenazi A. Control of TRAIL-induced apoptosis by
a family of signaling and decoy receptors. Science 1997;277:818-21

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IKKα (C1) peptide
CATALOG NO.: 2025P
SEQUENCE: CLGHLSTIIHEANEEQGNS
LOCATION: Amino acids 716 to 734 of human IKKα (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-IKKα (catalog number 2025). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A cytokine-responsive IkappaB kinase
that activates the transcription factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M. Identification and characterization of an
IkappaB kinase. Cell 1997;90:373-83

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ADAM10 (CT) peptide
CATALOG NO.: 2051P
SEQUENCE: PQRQRPRESYQMGHMRR
LOCATION: Amino acids 732 to 748 of human ADAM10 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ADAM10 (catalog number 2051). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Rosendahl MS, Ko SC, Long DL, et al. Identification and characterization of a pro-tumor necrosis
factor-alpha-processing enzyme from the ADAM family of zinc metalloproteases. J Biol Chem
1997;272:24588-93

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FLIPs (CT) peptide
CATALOG NO.: 2055P
SEQUENCE: QKSLKDPSNNFRMITPYAH
LOCATION: Amino acids 191 to 209of human FLIPs (1)
APPLICATION:
The peptide is used for blocking the activity of anti-FLIPs (catalog number 2055). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Irmler M, Thome M, Hahne M, Schneider P, Hofmann K, Steiner V, Bodmer JL, Schroter M, Burns K,
Mattmann C, Rimoldi D, French LE, Tschopp J. Inhibition of death receptor signals by cellular FLIP.
Nature 1997;388:190-195

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Suite 207
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www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
DNase II (CT) peptide
CATALOG NO.: 2059P
SEQUENCE: NH 2 -CNGMARKPSRAYKI-OH
LOCATION: Amino acids 347 to 360 of human DNase II precursor (1-3).
APPLICATION:
The peptide is used for blocking the antibody activity of DNase II (catalog number 2059). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Yasuda T, Takeshita H, Iida R, Nakajima T, Hosomi O, Nakashima Y, Kishi K. Molecular cloning
of the cDNA encoding human deoxyribonuclease II. J Biol Chem 1998;273:2610-6
2. Krieser RJ, Eastman A. The cloning and expression of human deoxyribonuclease II. A possible role
in apoptosis. J Biol Chem 1998;273:30909-14
3. Shiokawa D, Tanuma S. Cloning of cDNAs encoding porcine and human DNase II. Biochem
Biophys Res Commun 1998;247:864-9

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Bim (IN) peptide
CATALOG NO.: 2065P
SEQUENCE: AERPPQLRPGAPTSLQTEP
LOCATION: Amino acids 22 to 40 of human Bim (1)
APPLICATION:
The peptide is used for blocking the activity of anti-Bim (catalog number 2065). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. O'Connor,L., Strasser,A., O'Reilly,L.A., Hausmann,G., Adams,J.M., Cory,S. and Huang,D.C. Bim: a
novel member of the Bcl-2 family that promotes apoptosis. EMBO J. 1998;17:384-395

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ZIPK (IN) peptide
CATALOG NO.: 2067P
SEQUENCE: RRRNVRGEDSGRKPERRRLK
LOCATION: Amino acids 279 to 298 of human ZIPK (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ZIPK (catalog number 2067). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kawai T, Matsumoto M, Takeda K, Sanjo H, Akira S. ZIP kinase, a novel serine/threonine kinase which
mediates apoptosis. Mol Cell Biol 1998;18:1642-51

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Caspase-9 (IN1) peptide
CATALOG NO.: 2071P
SEQUENCE: EDIQRAGSGSRRDQAR
LOCATION: Amino acids 41 to 56 of human caspase-9 (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-caspase-9 (catalog number 2071). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Duan H, Orth K, Chinnaiyan AM, Poirier GG, Froelich CJ, He WW, Dixit VM. ICE-LAP6, a novel
member of the ICE/Ced-3 gene family, is activated by the cytotoxic T cell protease granzyme B. J Biol
Chem 1996;271:16720-4
2. Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, Robertson N, Armstrong RC, Wang L, Trapani JA,
Tomaselli KJ, Litwack G, Alnemri ES. The Ced-3/interleukin 1beta converting enzyme-like homolog
Mch6 and the lamin-cleaving enzyme Mch2alpha are substrates for the apoptotic mediator CPP32. J
Biol Chem 1996;271:27099-106
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M, Alnemri ES, Wang X. Cytochrome c and
dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade. Cell
1997;91:479-89

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Caspase-9 (IN2) peptide
CATALOG NO.: 2073P
SEQUENCE: ASTSPEDESPGSNPEPDATP
LOCATION: Amino acids 299 to 318 of human caspase-9 (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-caspase-9 (catalog number 2073). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Duan H, Orth K, Chinnaiyan AM, Poirier GG, Froelich CJ, He WW, Dixit VM. ICE-LAP6, a novel
member of the ICE/Ced-3 gene family, is activated by the cytotoxic T cell protease granzyme B. J Biol
Chem 1996;271:16720-4
2. Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, Robertson N, Armstrong RC, Wang L, Trapani JA,
Tomaselli KJ, Litwack G, Alnemri ES. The Ced-3/interleukin 1beta converting enzyme-like homolog
Mch6 and the lamin-cleaving enzyme Mch2alpha are substrates for the apoptotic mediator CPP32. J
Biol Chem 1996;271:27099-106
3. Li P, Nijhawan D, Budihardjo I, Srinivasula SM, Ahmad M, Alnemri ES, Wang X. Cytochrome c and
dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade. Cell
1997;91:479-89

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RICK (NT) peptide
CATALOG NO.: 2075P
SEQUENCE: PTIPYHKLADLRYLSRGASG
LOCATION: Amino acids 11 to 30 of human RICK (1)
APPLICATION:
The peptide is used for blocking the activity of anti-RICK (catalog number 2075). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Inohara N, del Peso L, Koseki T, Chen S, Nunez G. RICK, a novel protein kinase containing a caspase
recruitment domain, interacts with CLARP and regulates CD95-mediated apoptosis. J Biol Chem
1998;273:12296-300

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ARC (CT) peptide
CATALOG NO.: 2081P
SEQUENCE: PDPEPEPDFEERDESEDS
LOCATION: Amino acids 191 to 208 of human ARC (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ARC (catalog number 2081). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Koseki T, Inohara N, Chen S, Nunez G. ARC, an inhibitor of apoptosis expressed in skeletal muscle
and heart that interacts selectively with caspases. Proc Natl Acad Sci U S A 1998;95:5156-60

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CIDE-A (CT) peptide
CATALOG NO.: 2085P
SEQUENCE: DDKEERPSLRSQAKGRFT
LOCATION: Amino acids 200 to 217 of human CIDE-A (1)
APPLICATION:
The peptide is used for blocking the activity of anti-CIDE-A (catalog number 2085). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel family of cell death activators with
homology to the 45 kDa subunit of the DNA fragmentation factor. EMBO J 1998;17:2526-33

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mCIDE-A (CT) peptide
CATALOG NO.: 2089P
SEQUENCE: GDTEEQPSPKPSTKG
LOCATION: Amino acids 200 to 214 of murine CIDE-A (1)
APPLICATION:
The peptide is used for blocking the activity of anti-mCIDE-A (catalog number 2089). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel family of cell death activators with
homology to the 45 kDa subunit of the DNA fragmentation factor. EMBO J 1998;17:2526-33

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mCIDE-B (CT) peptide
CATALOG NO.: 2091P
SEQUENCE: EGADRWQWHGQRHLHS
LOCATION: Amino acids 204 to 219 of murine CIDE-B (1)
APPLICATION:
The peptide is used for blocking the activity of anti-mCIDE-B (catalog number 2091). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel family of cell death activators with
homology to the 45 kDa subunit of the DNA fragmentation factor. EMBO J 1998;17:2526-33

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CX 3 CR1 (NT) peptide
CATALOG NO.: 2093P
SEQUENCE: DQFPESVTENFEYDDLAEAC
LOCATION: Amino acids 2 to 21 of murine CX 3 CR1 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-CX 3 CR1 (catalog number 2093). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Raport CJ, Schweickart VL, Eddy RL JR, Shows TB, Gray PW. The orphan G-protein-coupled
receptor-encoding gene V28 is closely related to genes for chemokine receptors and is expressed in
lymphoid and neural tissues. Gene 1995;163:295-9
2. Combadiere C, Ahuja SK, Murphy PM. Cloning, chromosomal localization, and RNA expression of a
human beta chemokine receptor-like gene. DNA Cell Biol 1995;14:673-80

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CCR8 (EL) peptide
CATALOG NO.: 2097P
SEQUENCE: CYSFYNQQTLKWKIFTNFK
LOCATION: Amino acids 732 to 748 of human CCR8 (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-CCR8 (catalog number 2097). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Napolitano M, Zingoni A, Bernardini G, Spinetti G, Nista A, Storlazzi CT, Rocchi M, Santoni A.
Molecular cloning of TER1, a chemokine receptor-like gene expressed by lymphoid tissues. J Immunol
1996;157:2759-63
2. Zaballos A, Varona R, Gutierrez J, Lind P, Marquez G. Molecular cloning and RNA expression of two
new human chemokine receptor-like genes. Biochem Biophys Res Commun 1996;227:846-53
3. Samson M, Stordeur P, Labbe O, Soularue P, Vassart G, Parmentier M. Molecular cloning and
chromosomal mapping of a novel human gene, ChemR1, expressed in T lymphocytes and
polymorphonuclear cells and encoding a putative chemokine receptor. Eur J Immunol 1996;26:3021-8

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GPR15 (NT) peptide
CATALOG NO.: 2101P
SEQUENCE: YYATSPNSDIRETHSH
LOCATION: Amino acids 13 to 28 of murine GPR15 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-GPR15 (catalog number 2101). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Heiber M, Marchese A, Nguyen T, Heng HH, George SR, O'Dowd BF. A novel human gene encoding
a G-protein-coupled receptor (GPR15) is located on chromosome 3. Genomics 1996;32:462-5

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DFF40/CAD (I18) peptide
CATALOG NO.: 2107P
SEQUENCE: EGLESRFRNKSGYLRYS
LOCATION: Amino acids 147 to 164 of murine CAD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DFF40/CAD (catalog number 2107). Incubating
the peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody
activity in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S. A caspase-activated DNase that
degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998;391:43-50

13100 Kirkham Way
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Toll Free: 888-513-9525
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techsupport@prosci-inc.com
IKKα (C2) peptide
CATALOG NO.: 2115P
SEQUENCE: TPQDGETSAQMIEENLN
LOCATION: Amino acids 699 to 715 of human IKKα (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-IKKα (catalog number 2115). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A cytokine-responsive IkappaB kinase
that activates the transcription factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M. Identification and characterization of an
IkappaB kinase. Cell 1997;90:373-83

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Toll Free: 888-513-9525
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IKKα (C3) peptide
CATALOG NO.: 2117P
SEQUENCE: CTQSSARSLVGSSLEGA
LOCATION: Amino acids 658 to 674 of human IKKα (1-3)
APPLICATION:
The peptide is used for blocking the activity of anti-IKKα (catalog number 2117). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. DiDonato JA, Hayakawa M, Rothwarf DM, Zandi E, Karin M. A cytokine-responsive IkappaB kinase
that activates the transcription factor NF-kappaB. Nature 1997;388:548-54
2. Regnier CH, Song HY, Gao X, Goeddel DV, Cao Z, Rothe M. Identification and characterization of an
IkappaB kinase. Cell 1997;90:373-83

13100 Kirkham Way
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Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
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IKKβ (C3) peptide
CATALOG NO.: 2121P
SEQUENCE: CSKVRGPVSGSPDSMNASR
LOCATION: Amino acids 662 to 680 of human IKKβ (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-IKKβ (catalog number 2121). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Zandi E, Rothwarf DM, Delhase M, Hayakawa M, Karin M. The IkappaB kinase complex (IKK)
contains two kinase subunits, IKKalpha and IKKbeta, necessary for IkappaB phosphorylation and NFkappaB
activation. Cell 1997;91:243-52
2. Woronicz JD, Gao X, Cao Z, Rothe M, Goeddel DY. IkappaB kinase-beta: NF-kappaB activation and
complex formation with IkappaB kinase-alpha and NIK. Science 1997;278:866-9

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IRAK2 (C2) peptide
CATALOG NO.: 2123P
SEQUENCE: APWAGAATPLLPTENGEGR
LOCATION: Amino acids 546 to 564 of human IRAK2 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-IRAK2 (catalog number 2123). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member IRAK-2 and MyD88 as proximal
mediators of IL-1 signaling. Science 1997;278:1612-5

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MyD88 (IN) peptide
CATALOG NO.: 2125P
SEQUENCE: CDFQTKFALSLSPGAHD
LOCATION: Amino acids 233 to 248 of human MyD88 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-MyD88 (catalog number 2125). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Bonnert TP, Garka KE, Parnet P, Sonoda G, Testa JR, Sims JE. The cloning and characterization of
human MyD88: amember of an IL-1 receptor related family. FEBS Lett 1997;402:81-4

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MyD88 (CT) peptide
CATALOG NO.: 2127P
SEQUENCE: CTKSWFWTRLAKALSLP
LOCATION: Amino acids 279 to 296 of human MyD88 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-MyD88 (catalog number 2127). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Bonnert TP, Garka KE, Parnet P, Sonoda G, Testa JR, Sims JE. The cloning and characterization of
human MyD88: a member of an IL-1 receptor related family. FEBS Lett 1997;402:81-4

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Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
IL-1RAcP (C2) peptide
CATALOG NO.: 2129P
SEQUENCE: KWKGEKSKYPQGRFWK
LOCATION: Amino acids 525 to 540 of human IL-1RAcP (1)
APPLICATION:
The peptide is used for blocking the activity of anti-IL-1RAcP (catalog number 2129). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Greenfeder SA, Nunes P, Kwee L, Labow M, Chizzonite RA, Ju G. Molecular cloning and
characterization of a second subunit of the interleukin 1 receptor complex. J Biol Chem
1995;270:13757-65

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IL-1RAcP (CT) peptide
CATALOG NO.: 2131P
SEQUENCE: KKSPRRSSSDEQGLSYSSLKN
LOCATION: Amino acids 549 to 569 of human IL-1RAcP (1)
APPLICATION:
The peptide is used for blocking the activity of anti-IL-1RAcP (catalog number 2131). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Greenfeder SA, Nunes P, Kwee L, Labow M, Chizzonite RA, Ju G. Molecular cloning and
characterization of a second subunit of the interleukin 1 receptor complex. J Biol Chem
1995;270:13757-65

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www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
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techsupport@prosci-inc.com
APP (AβNT) peptide
CATALOG NO.: 2133P
SEQUENCE: DAEFRHDSGY
LOCATION: Amino acids 653 to 662 of human APP (1)
APPLICATION:
The peptide is used for blocking the activity of anti-APP (catalog number 2133). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Ponte P, Gonzalez-DeWhitt P, Schilling J, Miller J, Hsu D, Greenberg B, Davis K, Wallace W,
Lieberburg I, Fuller F. A new A4 amyloid mRNA contains a domain homologous to serine proteinase
inhibitors. Nature 1988;331:525-7.

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APP (CT) peptide
CATALOG NO.: 2136P
SEQUENCE: GYENPTYKFFEQMQN
LOCATION: Amino acids 737 to 751 of human APP (1)
APPLICATION:
The peptide is used for blocking the activity of anti-APP (catalog number 2136). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Ponte P, Gonzalez-DeWhitt P, Schilling J, Miller J, Hsu D, Greenberg B, Davis K, Wallace W,
Lieberburg I, Fuller F. A new A4 amyloid mRNA contains a domain homologous to serine proteinase
inhibitors. Nature 1988;331:525-7.

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Toll Free: 888-513-9525
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Fax: 858-513-2692
techsupport@prosci-inc.com
DcR3 (NT) peptide
CATALOG NO.: 2140P
SEQUENCE: AETPTYPWRDAETGERC
LOCATION: Amino acids 31 to 46 of human DcR3 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DcR3 (catalog number 2140). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pitti RM, Marsters SA, Lawrence DA, Roy M, Kischkel FC, Dowd P, Huang A, Donahue CJ, Sherwood SW,
Baldwin DT, Godowski PJ, Wood WI, Gurney AL, Hillan KJ, Cohen RL, Goddard AD, Botstein D, Ashkenazi A.
Genomic amplification of a decoy receptor for Fas ligand in lung and colon cancer. Nature 1998;396:699-703
2. Yu KY, Kwon B, Ni J, Zhai Y, Ebner R, Kwon BS. A newly identified member of tumor necrosis factor receptor
superfamily (TR6) suppresses LIGHT-mediated apoptosis. J Biol Chem 1999;274:13733-6

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SODD (NT) peptide
CATALOG NO.: 2143P
SEQUENCE: SALRRSGYGPSDGPSC
LOCATION: Amino acids 2 to 16 of human SODD (1)
APPLICATION:
The peptide is used for blocking the activity of anti-SODD (catalog number 2143). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Jiang Y, Woronicz JD, Liu W, Goeddel DY. Prevention of constitutive TNF receptor 1 signaling by
silencer of death domains. Science 1999;283:543-6

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DRAK1 (NT) peptide
CATALOG NO.: 2147P
SEQUENCE: EKPGSGGSSPGATSGC
LOCATION: Amino acids 5 to 19 of human DRAK1 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DRAK1 (catalog number 2147). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sanjo H, Kawai T, Akira S. DRAKs, novel serine/threonine kinases related to death-associated protein
kinase that trigger apoptosis. J Biol Chem 1998;273:29066-71

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DRAK2 (CT) peptide
CATALOG NO.: 2149P
SEQUENCE: CSKRFRFDDSLPNPHE
LOCATION: Amino acids 351 to 365 of human DRAK2 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DRAK2 (catalog number 2149). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sanjo H, Kawai T, Akira S. DRAKs, novel serine/threonine kinases related to death-associated protein
kinase that trigger apoptosis. J Biol Chem 1998;273:29066-71

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DFF40 (NT) peptide
CATALOG NO.: 2153P
SEQUENCE: QKPKSVKLRALRSPRKC
LOCATION: Amino acids 3 to 18 of human DFF40 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DFF40 (catalog number 2153). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The 40-kDa subunit of DNA
fragmentation factor induces DNA fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
2. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H, Nagata S. Molecular cloning and
characterization of human caspase-activated DNase. Proc Natl Acad Sci USA 1998;95:9123-8

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DFF40 (IN) peptide
CATALOG NO.: 2155P
SEQUENCE: NGSYFDRGAKGGSRLC
LOCATION: Amino acids 203 to 218 of human DFF40 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-DFF40 (catalog number 2155). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Liu X, Li P, Widlak P, Zou H, Luo X, Garrard WT, Wang X The 40-kDa subunit of DNA
fragmentation factor induces DNA fragmentation and chromatin condensation during apoptosis. Proc
Natl Acad Sci USA 1998;95:8461-6
2. Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H, Nagata S. Molecular cloning and
characterization of human caspase-activated DNase. Proc Natl Acad Sci USA 1998;95:9123-8

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DR6 (NT) peptide
CATALOG NO.: 2157P
SEQUENCE: QPEQKASNLIGTYRHC
LOCATION: Amino acids 42 to 56 of human DR6 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DR6 (catalog number 2157). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G, Bauer JH, Haridas V, Wang S, Liu D, Yu G, Vincenz C, Aggarwal BB, Ni J, Dixit VM.
Identification and functional characterization of DR6, a novel death domain-containing TNF receptor.
FEBS Lett 199;431:351-6

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BCL-10 (NT) peptide
CATALOG NO.: 2161P
SEQUENCE: APSLTEEDLTEVKKDC
LOCATION: Amino acids 5 to 19 of human BCL-10 (1-5)
APPLICATION:
The peptide is used for blocking the activity of anti-BCL-10 (catalog number 2161). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Willis TG, Jadayel DM, Du MQ, et al. Bcl10 is involved in t(1;14)(p22;q32) of MALT B cell lymphoma and
mutated in multiple tumor types. Cell 1999;96(1):35-45
2. Koseki T, Inohara N, Chen S, et al. CIPER, a novel NF kappaB-activating protein containing a caspase
recruitment domain with homology to Herpesvirus-2 protein E10. J Biol Chem 1999;274(15):9955-61
3. Yan M, Lee J, Schilbach S, Goddard A, Dixit V. mE10, a novel caspase recruitment domain-containing
proapoptotic molecule. J Biol Chem 1999;274(15):10287-92
4. Thome M, Martinon F, Hofmann K, et al. Equine herpesvirus-2 E10 gene product, but not its cellular homologue,
activates NF-kappaB transcription factor and c-Jun N-terminal kinase. J Biol Chem 1999;274(15):9962-8
5. Srinivasula SM, Ahmad M, Lin JH, et al. CLAP, a novel caspase recruitment domain-containing protein in the
tumor necrosis factor receptor pathway, regulates NF-kappaB activation and apoptosis. J Biol Chem
1999;274(25):17946-54

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DcR1 (ED) peptide
CATALOG NO.: 2179P
SEQUENCE: CVEEFGANATVETPAAEET
LOCATION: Amino acids 149 to 167 of human DcR1 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-DcR1 (catalog number 2179). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year..
REFERENCE:
1. Pan G, Ni J, Wei YF, et al. An antagonist decoy receptor and a death domain-containing receptor for
TRAIL. Science 1997;277:815-8
2. Sheridan JP, Marsters SA, Pitti RM, et al. A. Control of TRAIL-induced apoptosis by a family of
signaling and decoy receptors. Science 1997;277:818-21

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RICK (CT) peptide
CATALOG NO.: 2183P
SEQUENCE: KLKDNKQMGLQPYPE
LOCATION: Amino acids 508 to 522 of human RICK (1)
APPLICATION:
The peptide is used for blocking the activity of anti-RICK (catalog number 2183). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Inohara N, del Peso L, Koseki T, Chen S, Nunez G. RICK, a novel protein kinase containing a caspase
recruitment domain, interacts with CLARP and regulates CD95-mediated apoptosis. J Biol Chem
1998;273:12296-300

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ARC (NT) peptide
CATALOG NO.: 2185P
SEQUENCE: GNAQERPSETIDRERKR
LOCATION: Amino acids 2 to 18 of human ARC (1)
APPLICATION:
The peptide is used for blocking the activity of anti-ARC (catalog number 2185). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Koseki T, Inohara N, Chen S, Nunez G. ARC, an inhibitor of apoptosis expressed in skeletal muscle
and heart that interacts selectively with caspases. Proc Natl Acad Sci U S A 1998;95:5156-60

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CX 3 CR1 (EL) peptide
CATALOG NO.: 2201P
SEQUENCE: CLGDYPEVLQEIWPV
LOCATION: Amino acids 175 to 189 of human CX 3 CR1/V28 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-CX 3 CR1 (catalog number 2201). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Raport CJ, Schweickart VL, Eddy RL JR, Shows TB, Gray PW. The orphan G-protein-coupled
receptor-encoding gene V28 is closely related to genes for chemokine receptors and is expressed in
lymphoid and neural tissues. Gene 1995;163:295-9
2. Combadiere C, Ahuja SK, Murphy PM. Cloning, chromosomal localization, and RNA expression of a
human beta chemokine receptor-like gene. DNA Cell Biol 1995;14:673-80

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Bonzo (NT2) peptide
CATALOG NO.: 2209P
SEQUENCE: GFSSFNDSSQEEHQD
LOCATION: Amino acids 11 to 25 of human Bonzo/STRL33 (1,2)
APPLICATION:
The peptide is used for blocking the activity of anti-Bonzo (catalog number 2209). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Deng HK, Unutmaz D, KewalRamani VN, Littman DR. Expression cloning of new receptors used by
simian and human immunodeficiency viruses. Nature 1997;388:296-300
2. Liao F, Alkhatib G, Peden KW, Sharma G, Berger EA, Farber JM. STRL33, A novel chemokine
receptor-like protein, functions as a fusion cofactor for both macrophage-tropic and T cell line-tropic
HIV-1. J Exp Med 1997;185:2015-23

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IRAK2 (CT) peptide
CATALOG NO.: 2213P
SEQUENCE: READSSSEACVGLEPPQDVT
LOCATION: Amino acids 571 to 590 of human IRAK2 (1)
APPLICATION:
The peptide is used for blocking the activity of anti-IRAK2 (catalog number 2213). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Muzio M, Ni J, Feng P, Dixit VM. IRAK (Pelle) family member IRAK-2 and MyD88 as proximal
mediators of IL-1 signaling. Science 1997;278:1612-5

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Acinus (CP) peptide
CATALOG NO.: 2215P
SEQUENCE: NH 2 -TRTALHGVKWPQSNPK-OH
LOCATION: Amino acids 1065 to 1080 of human AcinusL, 338 to 353 of human AcinusS’, or 307 to 322
of human AcinusS, which are identical to those of mouse Acinus (1). The selected antigenic sequence is
located near the C-terminus of the cleaved active peptide p17.
APPLICATION:
The peptide is used for blocking the antibody activity of Acinus (catalog number 2215). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto Y. Acinus is a caspase-3-activated
protein required for apoptotic chromatin condensation. Nature 1999 401:168-73.

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Acinus (CT) peptide
CATALOG NO.: 2217P
SEQUENCE: NH 2 -SRSTPVRDRGGRR-OH
LOCATION: Amino acids 1329 to 1341 of human AcinusL, 602 to 614 of human AcinusS’, or 571 to 583
of human AcinusS (1).
Application:
The peptide is used for blocking the antibody activity of Acinus (catalog number 2217). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto Y. Acinus is a caspase-3-activated
protein required for apoptotic chromatin condensation. Nature 1999 401:168-73.

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Acinus (IN) peptide
CATALOG NO.: 2219P
SEQUENCE: NH 2 -DTSENRPENDVPEPP-OH
LOCATION: Amino acids 775 to 789 of human AcinusL, 48 to 62 of human AcinusS’, or 17 to 31 of
human AcinusS (1).
APPLICATION:
The peptide is used for blocking the antibody activity of Acinus (catalog number 2219). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto Y. Acinus is a caspase-3-activated
protein required for apoptotic chromatin condensation. Nature 1999 401:168-73.

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BAFF (CT) peptide
CATALOG NO.: 2221P
SEQUENCE: NH 2 -EEGDELQLAIPRENAQ-OH
LOCATION: Amino acids 254 to 269 of human BAFF/BLys (1,4)
APPLICATION:
The peptide is used for blocking the activity of BAFF (catalog number 2221). It usually blocks the
antibody activity completely in Western blot by incubating the peptide with equal volume of antibody for
30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Moore PA, Belvedere O, Orr A, et al. BLyS: member of the tumor necrosis factor family and B
lymphocyte stimulator. Science 1999;285:260-3
2. Schneider P, MacKay F, Steiner V, et al. BAFF, a novel ligand of the tumor necrosis factor family,
stimulates B cell growth. J Exp Med 1999;189:1747-56
3. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the TNF family that is down-regulated by
mitogens. J Leukoc Biol 1999;65:680-3
4. Mukhopadhyay A, Ni J, Zhai Y, Yu GL, Aggarwal BB. Identification and characterization of a novel
cytokine, THANK, a TNF homologue that activates apoptosis, nuclear factor-kappaB, and c-Jun NH2-
terminal kinase. J Biol Chem 1999 ;274:15978-81

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CATALOG NO.: 2223P
SEQUENCE: NH 2 -GTGGPSQNGEGYP-OH
APRIL (ED) (TALL-2/TRDL-1) peptide
LOCATION: Amino acids 67 to 79 of human APRIL (1-3).
APPLICATION:
The peptide is used for blocking the antibody activity of APRIL (catalog number 2423). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Hahne M, Kataoka T, Schroter M, et al. APRIL, a new ligand of the tumor necrosis factor
family, stimulates tumor cell growth. J Exp Med. 1998;188(6):1185-90.
2. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the TNF family that is downregulated
by mitogens. J Leukoc Biol. 1999;65(5):680-3.
3. Kelly K, Manos E, Jensen G, et al. APRIL/TRDL-1, a tumor necrosis factor-like ligand,
stimulates cell death. Cancer Res. 2000;60(4):1021-7.

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DEDAF peptide
CATALOG NO.: 2227P
SEQUENCE: NH 2 -TPKGDMSAVNDESF-OH
LOCATION: Amino acids 215 to 228 of human DADEF (1)
APPLICATION:
The peptide is used for blocking the activity of DEDAF (catalog number 2227). It usually blocks the
antibody activity completely in Western blot by incubating the peptide with equal volume of antibody for
30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Zheng L, Schickling O, Peter ME, Lenardo MJ. The death effector domain-associated factor plays
distinct regulatory roles in the nucleus and cytoplasm. J Biol Chem. 2001;276(34):31945-52.

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Survivin (NT) peptide
CATALOG NO.: 2233P
SEQUENCE: NH 2 -MGAPTLPPAWQP-OH
LOCATION: Amino acids 1 to 12 of human survivin (1).
APPLICATION:
The peptide is used for blocking the antibody activity of survivin (catalog number 2233). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene, survivin, expressed in cancer and
lymphoma. Nat Med 1997;3:917-21

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Survivin (CT) peptide
CATALOG NO.: 2235P
SEQUENCE: NH 2 -KKVRRAIEQLAAMD-OH
LOCATION: Amino acids 129 to 142 of human survivin (1).
APPLICATION:
The peptide is used for blocking the antibody activity of survivin (catalog number 2235). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene, survivin, expressed in cancer and
lymphoma. Nat Med 1997;3:917-21

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Survivin (CT) peptide
CATALOG NO.: 2237P
SEQUENCE: NH 2 -AKTTRQSIEQLAA-OH
LOCATION: Amino acids 128 to 140 of mouse survivin (1).
APPLICATION:
The peptide is used for blocking the antibody activity of survivin (catalog number 2237). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kobayashi K, Hatano M, Otaki M, Ogasawara T, Tokuhisa T. Expression of a murine homologue
of the inhibitor of apoptosis protein is related to cell proliferation. Proc Natl Acad Sci USA 1999;96:1457-
62

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AIF (NT) peptide
CATALOG NO.: 2239P
SEQUENCE: NH 2 -KQKKAALSASEGEE-OH
LOCATION: Amino acids 109 to 122 of human AIF (1).
APPLICATION:
The peptide is used for blocking the antibody activity of AIF (catalog number 2239). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosisinducing
factor. Nature 1999;397:441-6

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Acinus (NP) peptide
CATALOG NO.: 2241P
SEQUENCE: NH 2 -DDPVRTAQVPSPPRGK-OH
LOCATION:
Amino acids 994 to 1009 of human AcinusL, 267 to 282 of human AcinusS’, or 236 to 251 of human
AcinusS, which are identical to those of mouse Acinus (1). The selected antigenic sequence is located near
the N-terminus of active peptide p17.
APPLICATION:
The peptide is used for blocking the antibody activity of Acinus (catalog number 2241). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto Y. Acinus is a caspase-3-activated
protein required for apoptotic chromatin condensation. Nature 1999 401:168-73.

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Caspase-13 peptide
CATALOG NO.: 2245P
SEQUENCE: NH 2 -ETVAGPDESVGSAAT-OH
LOCATION: Amino acids 91 to 105 of human Acaspase-13 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of caspase-13 (catalog number 2245). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Humke EW, Ni J, Dixit VM. ERICE, a novel FLICE-activatable caspase. J Biol Chem
1998;273:15702-7

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BACE2 (NT) peptide
CATALOG NO.: 2247P
SEQUENCE: NH 2 -APTPGPGTPAERHADG-OH
LOCATION: Amino acids 44 to 59 of human BACE2 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of BACE2 (catalog number 2247). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Yan R, et al. Membrane-anchored aspartyl protease with Alzheimer's disease beta-secretase activity.
Nature 1999;402:533-7

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BACE2 (CT) peptide
CATALOG NO.: 2249P
SEQUENCE: NH 2 -CQRRPRDPEVVNDESS-OH
LOCATION: Amino acids 496 to 511 of human BACE2 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of BACE2 (catalog number 2249). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Yan R, et al. Membrane-anchored aspartyl protease with Alzheimer's disease beta-secretase activity.
Nature 1999;402:533-7

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BACE (CT) peptide
CATALOG NO.: 2253P
SEQUENCE: NH 2 -CLRQQHDDFADDISLLK-OH
LOCATION: Amino acids 485 to 501 of human BACE (1).
APPLICATION:
The peptide is used for blocking the antibody activity of BACE (catalog number 2253). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Vassar R, Bennett BD, Babu-Khan S, et al. Beta-secretase cleavage of Alzheimer's amyloid
precursor protein by the transmembrane aspartic protease BACE. Science 1999;286:735-41

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AIF (IN) peptide
CATALOG NO.: 2267P
SEQUENCE: NH 2 -PKSATEQSGTGIRSE-OH
LOCATION:
Amino acids 517 to 531 of human AIF, which are identical to corresponding amino acids of mouse and
rat AIF (1).
APPLICATION:
The peptide is used for blocking the antibody activity of AIF (catalog number 2267). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosisinducing
factor. Nature 1999;397:441-6

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FLASH (CT) peptide
CATALOG NO.: 2271P
SEQUENCE: NH 2 -SERFQQLMKLFEKSKC-OH
LOCATION: Amino 1253 to 1268 of human FLASH (1).
APPLICATION:
The peptide is used for blocking the antibody activity of FLASH (catalog number 2271). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Koonin EV, Aravind L, Hofmann K, Tschopp J, Dixit VM Apoptosis. Searching for FLASH domains.
Nature 1999;401:662-3

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F1Aα peptide
CATALOG NO.: 2279P
SEQUENCE: NH 2 -DINYQDQIPRTLEE-OH
LOCATION: Amino acids 609 to 622 of human F1Aα, ?which are identical to the corresponding
sequences of mouse FEM1β (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of F1Aα (catalog number 2279). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Chan SL, Tan KO, Zhang L, Yee KS, Ronca F, Chan MY, Yu VC. F1Aalpha, a death receptor-binding
protein homologous to the Caenorhabditis elegans sex-determining protein, FEM-1, is a caspase substrate
that mediates apoptosis. J Biol Chem. 1999;274(45):32461-8.
2. Ventura-Holman T, Maher JF. Sequence, organization, and expression of the human FEM1B gene.
Biochem Biophys Res Commun 2000;267(1):317-20

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RIP3 peptide
CATALOG NO.: 2283P
SEQUENCE: NH 2 -AQFGRGRGWQPFHK-OH
LOCATION: Amino acids 473 to 486 of murine RIP3 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of RIP3 (catalog number 2283). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pazdernik NJ, Donner DB, Goebl MG, Harrington MA. Mouse receptor interacting protein 3 does not
contain a caspase-recruiting or a death domain but induces apoptosis and activates NF-? B. Mol Cell Biol.
1999;19(10):6500-8.

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ASC peptide
CATALOG NO.: 2287P
SEQUENCE: NH 2 -RESQSYLVEDLERS-OH
LOCATION: Amino acids 182 to 195 of human ASC (1).
APPLICATION:
The peptide is used for blocking the antibody activity of ASC (catalog number 2287). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Masumoto J, Taniguchi S, Ayukawa K, Sarvotham H, Kishino T, Niikawa N, Hidaka E, Katsuyama T,
Higuchi T, Sagara J. ASC, a novel 22-kDa protein, aggregates during apoptosis of human promyelocytic
leukemia HL-60 cells. J Biol Chem. 1999;274(48):33835-8.

13100 Kirkham Way
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Toll Free: 888-513-9525
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Bnip3L (IN) peptide
CATALOG NO.: 2289P
SEQUENCE: NH 2 -DAQHESGQSSSRGSSH-OH
LOCATION: Amino acids 77 to 92 of human origin, which are identical to those of mouse Bnip3L (1).
APPLICATION:
The peptide is used for blocking the antibody activity of Bnip3L (catalog number 2289). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Chen G, Cizeau J, Vande Velde C, et al. Nix and Nip3 form a subfamily of pro-apoptotic mitochondrial
proteins. J Biol Chem 1999;274(1):7-10

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DcR1 (ED2) peptide
CATALOG NO.: 2299P
SEQUENCE: NH 2 -CKEGTFRNENSPE-OH
LOCATION: Amino acids 111 to 123 at extracellular domain of human DcR1 precursor (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of DcR1 (catalog number 2299). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pan G, Ni J, Wei YF, et al. An antagonist decoy receptor and a death domain-containing receptor for
TRAIL. Science 1997;277:815-8
3. Sheridan JP, Marsters SA, Pitti RM, et al. A. Control of TRAIL-induced apoptosis by a family of
signaling and decoy receptors. Science 1997;277:818-21

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Toll Free: 888-513-9525
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AIF (CT) peptide
CATALOG NO.: 2301P
SEQUENCE: NH 2 -KDGEQHEDLNEVAK-OH
LOCATION: Amino acids 593 to 606 of human AIF (1).
APPLICATION:
The peptide is used for blocking the antibody activity of AIF (catalog number 2301). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosisinducing
factor. Nature 1999;397:441-6

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
DAP Kinase 2 peptide
CATALOG NO.: 2323P
SEQUENCE: NH 2 -ARRKALHPRRRSSTS-OH
LOCATION: Amino acids 356 to 370 of human DAPK2 (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of DAP kinase 2 (catalog number 2323). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with equal
volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Kawai T, Nomura F, Hoshino K, Copeland NG, Gilbert DJ, Jenkins NA, Akira S. Death-associated
protein kinase 2 is a new calcium/calmodulin-dependent protein kinase that signals apoptosis through its
catalytic activity. Oncogene 1999;18(23):3471-80
2. Inbal B, Shani G, Cohen O, Kissil JL, Kimchi A. Death-associated protein kinase-related protein 1, a
novel serine/threonine kinase involved in apoptosis. Mol Cell Biol 2000;20(3):1044-54

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Caspase-12 (NT) peptide
CATALOG NO.: 2325P
SEQUENCE: NH 2 -AARRTHERDPIYKIKG-OH
LOCATION: Amino acids 2 to 17 of murine caspase-12 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of caspase-12 (catalog number 2325). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA, Yuan J. Caspase-12 mediates endoplasmicreticulum-specific
apoptosis and cytotoxicity by amyloid-beta. Nature 2000;403:98-103.

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Caspase-12 (IN) peptide
CATALOG NO.: 2327P
SEQUENCE: NH 2 -CTPSSPSESKRKVEDDE-OH
LOCATION: Amino acids 100 to 116 of murine caspase-12 (1).
APPLICATION:
The peptide is used for blocking the antibody activity of caspase-12 (catalog number 2327). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA, Yuan J. Caspase-12 mediates endoplasmicreticulum-specific
apoptosis and cytotoxicity by amyloid-beta. Nature 2000;403:98-103.

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Toll Free: 888-513-9525
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techsupport@prosci-inc.com
IKKε/IKK-i (CT) peptide
CATALOG NO.: 2329P
SEQUENCE: NH 2 -NRIIERLNRVPAPPDV-OH
LOCATION: Amino acids 701 to 716 of human IKKε/IKK-i (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of IKKε/IKK-i (catalog number 2329). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Peters RT, Liao SM, Maniatis T. IKKepsilon is part of a novel PMA-inducible IkappaB kinase complex.
Mol Cell 2000;5(3):513-22
2. Shimada T, Kawai T, Takeda K, Matsumoto M, Inoue J, Tatsumi Y, Kanamaru A, Akira S. IKK-i, a
novel lipopolysaccharide-inducible kinase that is related to IkappaB kinases. Int Immunol 1999;11(8):1357-
62

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IKKγ/NEMO (NT) peptide
CATALOG NO.: 2335P
SEQUENCE: NH 2 -CQYQAPDMDTLQIHVME-OH
LOCATION: Amino acids 400 to 416 of human IKKγ (1,2)
APPLICATION:
The peptide is used for blocking the antibody activity of IKKγ (catalog number 2335). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Rothwarf DM, Zandi E, Natoli G, Karin M. IKK-gamma is an essential regulatory subunit of the
IkappaB kinase complex. Nature 1998;395(6699):297-300
2. Yamaoka S, Courtois G, Bessia C, Whiteside ST, Weil R, Agou F, Kirk HE, Kay RJ, Israel A.
Complementation cloning of NEMO, a component of the IkappaB kinase complex essential for NF-kappaB
activation. Cell. 1998;93(7):1231-40.

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DC-SIGN (CT) peptide
CATALOG NO.: 2347P
SEQUENCE: NH 2 -CSRDEEQFLSPAPATPNPPPA-OH
LOCATION: Amino acids 384 to 404 of human DC-DIGN (1).
Application:
The peptide is used for blocking the antibody activity of DC-SIGN (catalog number 2347). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with an
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Geijtenbeek TB, Kwon DS, Torensma R, et al. DC-SIGN, a dendritic cell-specific HIV-1-
binding protein that enhances trans-infection of T cells. Cell. 2000;100:587-97.

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DC-SIGN (ED) peptide
CATALOG NO.: 2349P
SEQUENCE: NH 2 -CYFMSNSQRNWHDSITA-OH
LOCATION: Amino acids 277 to 293 of human DC-DIGN (1).
Application:
The peptide is used for blocking the antibody activity of DC-SIGN (catalog number 2347). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Geijtenbeek TB, Kwon DS, Torensma R, et al. DC-SIGN, a dendritic cell-specific HIV-1-
binding protein that enhances trans-infection of T cells. Cell. 2000;100:587-97.

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techsupport@prosci-inc.com
NAK/TBK1 (CT) peptide
CATALOG NO.: 2351P
SEQUENCE: NH 2 -ERFGSLTMDGGLRNVD-OH
LOCATION: Amino acids 712 to 727 of human NAK/TBK1 (1,2)
APPLICATION:
The peptide is used for blocking the antibody activity of NAK/TBK1 (catalog number 2351). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with an equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Pomerantz JL, Baltimore D. NF-kappaB activation by a signaling complex containing TRAF2, TANK
and TBK1, a novel IKK-related kinase. EMBO J 1999;18(23):6694-704
2. Tojima Y, Fujimoto A, Delhase M, Chen Y, Hatakeyama S, Nakayama K, Kaneko Y, Nimura Y,
Motoyama N, Ikeda K, Karin M, Nakanishi M. NAK is an IkappaB kinase-activating kinase. Nature
2000;404(6779):778-82

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IRAK-M peptide
CATALOG NO.: 2355P
SEQUENCE: NH 2 -CSSKFSWDEYEQYKKE-OH
LOCATION: Amino acids 581 to 596 of human IRAK-M (1)
APPLICATION:
The peptide is used for blocking the antibody activity of IRAK-M (catalog number 2255). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Wesche H, Gao X, Li X, Kirschning CJ, Stark GR, Cao Z. IRAK-M is a novel member of the
Pelle/interleukin-1 receptor-associated kinase (IRAK) family. J Biol Chem. 1999;274(27):19403-10.

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p53R2 (NT) peptide
CATALOG NO.: 2383P
SEQUENCE: NH 2 -GDPERPEAAGLDQDER-OH
LOCATION: Amino acids 2 to 17 of human p53R2 (1)
APPLICATION:
The peptide is used for blocking the antibody activity of p53R2 (catalog number 2383). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle regulation by the Chk2 protein kinase.
Science. 1998;282:1893-7.

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Chk2 (NT) peptide
CATALOG NO.: 2391P
SEQUENCE: NH 2 -SRESDVEAQQSHGSSAC-OH
LOCATION: Amino acids 2 to 18 of human Chk2 (1)
APPLICATION:
The peptide is used for blocking the antibody activity of Chk2 (catalog number 2391). It usually blocks
the antibody activity completely in Western blot by incubating the peptide with equal volume of antibody
for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Matsuoka S, Huang M, Elledge SJ. Linkage of ATM to cell cycle regulation by the Chk2 protein kinase.
Science. 1998;282:1893-7.

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Smac/DIABLO (CT) peptide
CATALOG NO.: 2409P
SEQUENCE: NH 2 -EERAESEQEAYLRED-OH
LOCATION: Amino acids 225 to 239 of human Smac/DIABLO (1)
APPLICATION:
The peptide is used for blocking the antibody activity of mSmac/DIABLO (catalog number 2409). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with equal
volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein that promotes cytochrome c-
dependent caspase activation by eliminating IAP inhibition. Cell. 2000;102(1):33-42.

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mSmac/DIABLO (CT) peptide
CATALOG NO.: 2411P
SEQUENCE: NH 2 - SDEGADQEEEAYLRED-OH
LOCATION: Amino acids 222 to 237 of murine Smac/DIABLO (1)
APPLICATION:
The peptide is used for blocking the antibody activity of mSmac/DIABLO (catalog number 2411). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with equal
volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Verhagen AM, Ekert PG, Pakusch M, Silke J, Connolly LM, Reid GE, Moritz RL, Simpson RJ, Vaux
DL. Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and
antagonizing IAP proteins. Cell. 2000;102(1):43-53.

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CATALOG NO.: 2415P
APRIL (ED2) (TALL-2/TRDL-1) peptide
SEQUENCE: NH 2 -CIRSMPSHPDRAYNS-OH
LOCATION: Amino acids 196 to 210 of human APRIL (1-3).
Application:
The peptide is used for blocking the antibody activity of APRIL (catalog number 2415). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Hahne M, Kataoka T, Schroter M, et al. APRIL, a new ligand of the tumor necrosis factor
family, stimulates tumor cell growth. J Exp Med. 1998;188(6):1185-90.
2. Shu HB, Hu WH, Johnson H. TALL-1 is a novel member of the TNF family that is downregulated
by mitogens. J Leukoc Biol. 1999;65(5):680-3.
3. Kelly K, Manos E, Jensen G, et al. APRIL/TRDL-1, a tumor necrosis factor-like ligand,
stimulates cell death. Cancer Res. 2000;60(4):1021-7.

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PID/MTA2 peptide
CATALOG NO.: 2443P
SEQUENCE: PAPSHPASTNEPIVLED
LOCATION: Amino acids 652 to 668 of human PID/MTA2 (1)
APPLICATION:
The peptide is used for blocking the activity of PID/MTA2 (catalog number 2443). Incubating the
peptide with equal volume of antibody for 30 min at 37°C usually completely blocks the antibody activity
in Western blotting.
For research use only.
STORAGE:
It is supplied as 200 µg/ml, 50 µg/vial, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53 modulates its effect on cell growth and
apoptosis. Nature. 2000;408:377-81.

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MTBP (IN2) peptide
CATALOG NO.: 2447P
SEQUENCE: NH 2 -GAVECFEEEDSNSRESLS-OH
LOCATION: Amino acids 122 to 139 of human MTBP (1).
APPLICATION:
The peptide is used for blocking the antibody activity of MTBP (catalog number 2247). It usually
blocks the antibody activity completely in Western blot by incubating the peptide with equal volume of
antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130 mM
NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C, stable for one year.
REFERENCE:
1. Boyd MT, Vlatkovic N, Haines DS. A novel cellular protein (MTBP) binds to MDM2 and induces a
G1 arrest that is suppressed by MDM2. J Biol Chem. 2000;275(41):31883-90.

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PERP peptide
CATALOG NO.: 2451P
SEQUENCE: NH 2 -EDDLLGNAKPRYFYTSA-OH
LOCATION: Amino acids 175 to 193 of human PERP (1,2).
Application:
The peptide is used for blocking the antibody activity of PERP (catalog number 2451). It can
block the antibody activity completely in Western blot by incubating the peptide with equal volume
of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Boyd MT, Vlatkovic N, Haines DS. A novel cellular protein (MTBP) binds to MDM2 and
induces a G1 arrest that is suppressed by MDM2. J Biol Chem. 2000;275(41):31883-90.
2. Attardi,L.D., Reczek,E.E., Cosmas,C., et al. PERP, an apoptosis-associated target of p53,
is a novel member of the PMP-22/gas3 family. Genes Dev. 2000;14 (6):704-718

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IL-21 (IN) peptide
CATALOG NO.: 2465P
SEQUENCE: NH 2 -TCPSCDSYEKKPPKE-OH
LOCATION: Amino acids 121 to 135 of human IL-21 precursor (1).
APPLICATION:
The peptide is used for blocking the antibody activity of IL-21 (catalog number 2465). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Arrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and its receptor are involved in NK
cell expansion and regulation of lymphocyte function. Nature. 2000;408(6808):57-63.

13100 Kirkham Way
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IL-21R (ED) peptide
CATALOG NO.: 2469P
SEQUENCE: NH 2 -NITDQSGNYSQECGS-OH
LOCATION: Amino acids 97 to 111 of human IL-21R precursor (1).
APPLICATION:
The peptide is used for blocking the antibody activity of IL-21R (catalog number 2469). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Arrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and its receptor are involved in NK
cell expansion and regulation of lymphocyte function. Nature. 2000;408(6808):57-63.

13100 Kirkham Way
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IL-21R (NT) peptide
CATALOG NO.: 2471P
SEQUENCE: NH 2 -CPDLVCYTDYLQT-OH
LOCATION: Amino acids 20 to 32 of human IL-21R precursor (1).
APPLICATION:
The peptide is used for blocking the antibody activity of IL-21R (catalog number 2471). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Arrish-Novak J, Dillon SR, Nelson A, et al. Interleukin 21 and its receptor are involved in NK
cell expansion and regulation of lymphocyte function. Nature. 2000;408(6808):57-63.

13100 Kirkham Way
Suite 207
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IL-22R (CT) peptide
CATALOG NO.: 2489P
SEQUENCE: NH 2 -DSLFRGLALTVQWES-OH
LOCATION: Amino acids 560 to 574 of human IL-22R precursor (1).
APPLICATION:
The peptide is used for blocking the antibody activity of IL-22R (catalog number 2489). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Dumoutier L, Louahed J, Renauld JC. Cloning and characterization of IL-10-related T cellderived
inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9. J
Immunol. 2000;164(4):1814-9.

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IL-22R (NT) peptide
CATALOG NO.: 2497P
SEQUENCE: NH 2 -QSSNFENILTWDSGPE-OH
LOCATION: Amino acids 31 to 46 of human IL-22R precursor (1).
APPLICATION:
The peptide is used for blocking the antibody activity of IL-22R (catalog number 2497). It
usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Dumoutier L, Louahed J, Renauld JC. Cloning and characterization of IL-10-related T cellderived
inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9. J
Immunol. 2000;164(4):1814-9.

13100 Kirkham Way
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techsupport@prosci-inc.com
CIKS/Act1 (CT) peptide
CATALOG NO.: 2499P
SEQUENCE: NH 2 -REEEYVAPPRGPLPT-OH
LOCATION: Amino acids 554 to 568 of human CIKS (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of CIKS/Act1 (catalog number 2499).
It usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Leonardi A, Chariot A, Claudio E, Cunningham K, Siebenlist U. CIKS, a connection to
Ikappa B kinase and stress-activated protein kinase. Proc Natl Acad Sci USA. 2000;97(19):10494-9.
2. Li X, Commane M, Nie H, Hua X, Chatterjee-Kishore M, Wald D, Haag M, Stark GR.
Act1, an NF-kappa B activating protein. Proc Natl Acad Sci USA. 2000;97(19):10489-93.

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CIKS/Act1 (NT) peptide
CATALOG NO.: 2501P
SEQUENCE: NH 2 -PPQLQETRMNRSIP-OH
LOCATION: Amino acids 2 to 15 of human CIKS (1,2).
APPLICATION:
The peptide is used for blocking the antibody activity of CIKS/Act1 (catalog number 2501).
It usually blocks the antibody activity completely in Western blot by incubating the peptide with
equal volume of antibody for 30 min at 37°C
For research use only.
STORAGE:
It is supplied as 50 µg at 200 µg/ml, in PBS pH7.2 (10 mM NaH 2 PO 4 , 10 mM Na 2 HPO 4 , 130
mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide. Store at -20°C,
stable for one year.
REFERENCE:
1. Leonardi A, Chariot A, Claudio E, Cunningham K, Siebenlist U. CIKS, a connection to
Ikappa B kinase and stress-activated protein kinase. Proc Natl Acad Sci USA. 2000;97(19):10494-9.
2. Li X, Commane M, Nie H, Hua X, Chatterjee-Kishore M, Wald D, Haag M, Stark GR.
Act1, an NF-kappa B activating protein. Proc Natl Acad Sci USA. 2000;97(19):10489-93.

lysate Data Sheets

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HeLa Cell Lysate
Catalog No: 1201
Cell line:
HeLa-S3 (Human cervix epithelioid carcinoma)
Growth media: Jokliks-MEM and 5% NCS (Newborn calf serum).
Cell lysate preparation:
HeLa cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
HeLa cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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A431 Cell Lysate
Catalog No: 1202
Cell line:
A431 (Human epidermoid carcinoma)
Growth media: DMEM and 10% FBS.
Cell lysate preparation:
A431 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
A431 cell lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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A549 Cell Lysate
Catalog No: 1203
Cell line:
A549 (Human lung carcinoma)
Growth media: DMEM and 10% NCS (Newborn calf serum)
Cell lysate preparation:
A549 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
A549 cell lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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K562 Cell Lysate
Catalog No: 1204
Cell line:
K562 (Human chronic myelogenous leukemia)
Growth media: RPMI & 10% NCS (Newborn calf serum)
Cell lysate preparation:
K562 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
K562 cell lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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Jurkat Cell Lysate
Catalog No: 1205
Cell line:
Jurkat, clone E6-1 (Human acute T cell leukemia)
Growth media: RPMI & 10% NCS (Newborn calf serum)
Cell lysate preparation:
Jurkat cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Jurkat cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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MOLT4 Cell Lysate
Catalog No: 1206
Cell line:
MOLT4 (Human acute lymphoblastic leukemia)
Growth media: RPMI and 10% FBS
Cell lysate preparation:
MOLT4 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
MOLT4 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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Raji Cell Lysate
Catalog No: 1207
Cell line:
Raji (Human Burkitt's lymphoma)
Growth media: RPMI & 10% NCS (Newborn calf serum)
Cell lysate preparation:
Raji cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Raji cell lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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THP-1 Cell Lysate
Catalog No: 1208
Cell line:
THP-1 (Human monocyte)
Growth media: RPMI & 10% FBS
Cell lysate preparation:
THP-1 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
THP-1 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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HL60 Cell Lysate
Catalog No: 1209
Cell line:
HL60 (Human promyelocytic leukemia)
Growth media: RPMI & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
HL60 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
HL60 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing 5%
β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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293 Cell Lysate
Catalog No: 1210
Cell line:
293 (Human transformed primary embryonal kidney)
Growth media: RPMI & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
293 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
293 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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HepG2 Cell Lysate
Catalog No: 1211
Cell line:
HepG2 (Human hepatocellular carcinoma)
Growth media: DMEM & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
HepG2 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium
chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
HepG2 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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3T3 Cell Lysate
Catalog No: 1212
Cell line:
BALB/3T3 clone A31 (Mouse embryo)
Growth media: DMEM & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
BALB/3T3 clone A31 cell lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
BALB/3T3 clone A31 cell lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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T24 Cell Lysate
Catalog No: 1213
Cell line:
T24 (Transitional-cell human bladder carcinoma)
Growth media: DMEM & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
T24 (Transitional-cell human bladder carcinoma) cell lysate was prepared by homogenization
in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM
ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1%
sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin).
Cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad
protein assay. The cell lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH
6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-
mercaptoethanol.
Application:
T24 (Transitional-cell human bladder carcinoma) cell lysate is ready to load on SDS-PAGE
for Western blotting, 20 µg per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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SW1353 Cell Lysate
Catalog No: 1214
Cell line:
SW1353 (Human humerus chondrosarcoma)
Growth media: DMEM & 10% FBS (Fetal bovine serum)
Cell lysate preparation:
SW1353 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
SW1353 cell lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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U937 Whole Cell Lysate
Catalog No: 1215
Cell line:
U937 (Human histiocytic lymphoma)
Growth media: DMEM & 10% NCS (Newborn Calf serum)
Cell lysate preparation:
U937 (Human histiocytic lymphoma) cell lysate was prepared by homogenization in modified
RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic
acid, 1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1%
sodium dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate
was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
U937 (Human histiocytic lymphoma) cell lysate is ready to load on SDS -PAGE for Western
blotting, 20 µg per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate, 200 µg per vial at 100 µg at 2 mg/ml, in 1 x SDS sample
buffer containing 5% β-mercaptoethanol. Storage at -20°C will be stable for three months, storage
at –70°C will be stable for one year.
For research use only.

13100 Kirkham Way
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PC-3 Whole Cell Lysate
Catalog No: 1216
Cell line:
PC-3 (Human prostate adenocarcinoma)
Growth media: DMEM/Hams F12 & 10% NCS (Newborn Calf serum)
Cell lysate preparation:
PC-3 (Human prostate adenocarcinoma) cell lysate was prepared by homogenization in
modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM
ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1%
sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin).
Cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad
protein assay. The cell lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH
6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-
mercaptoethanol.
Application:
PC-3 (Human prostate adenocarcinoma) cell lysate is ready to load on SDS-PAGE for
Western blotting, 20 µg per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate, 200 µg per vial at 100 µg at 2 mg/ml, in 1 x SDS sample
buffer containing 5% β-mercaptoethanol. Storage at -20°C will be stable for three months, storage
at –70°C will be stable for one year.
For research use only.

13100 Kirkham Way
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MDA-MB-361 Whole Cell Lysate
Catalog No: 1217
Cell line:
MDA-MB-361 (Human breast adenocarcinoma)
Growth media: DMEM/Hams F12 & 10% NCS (Newborn Calf serum)
Cell lysate preparation:
MDA-MB-361 (Human breast adenocarcinoma) cell lysate was prepared by homogenization
in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM
ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1%
sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin).
Cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad
protein assay. The cell lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH
6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-
mercaptoethanol.
Application:
MDA-MB-361 (Human breast adenocarcinoma) cell lysate is ready to load on SDS-PAGE for
Western blotting, 20 µg per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate, 200 µg per vial at 100 µg at 2 mg/ml, in 1 x SDS sample
buffer containing 5% β-mercaptoethanol. Storage at -20°C will be stable for three months, storage
at –70°C will be stable for one year.
For research use only.

13100 Kirkham Way
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Human Heart Tissue Lysate
Catalog No: 1301
Source: 38 year old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human heart tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human heart tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Lung Tissue Lysate
Catalog No: 1302
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human lung tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human lung tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Brain Tissue Lysate
Catalog No: 1303
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human brain tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human brain tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Liver Tissue Lysate
Catalog No: 1304
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human liver tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human liver tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Kidney Tissue Lysate
Catalog No: 1305
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human kidney tissue lysate was prepared by homogenization in modified RIPA buffer (150
mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human kidney tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Spleen Tissue Lysate
Catalog No: 1306
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human spleen tissue lysate was prepared by homogenization in modified RIPA buffer (150
mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human spleen tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Human Pancreas Tissue Lysate
Catalog No: 1307
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human pancreas tissue lysate was prepared by homogenization in modified RIPA buffer (150
mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human pancreas tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
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Catalog No: 1308
Human Small Intestine Tissue Lysate
Source: 38-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human small intestine tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human small intestine tissue lysate is ready to load on SDS -PAGE for Western blotting, 20
µg per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
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Catalog No: 1321
Human Lung Tumor Tissue Lysate
Source: 28-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human lung tumor (adenocarcinoma) tissue lysate was prepared by homogenization in lysis
buffer (10 mM HEPES pH7.9, 1.5 mM MgCl 2 , 10 mM KCl, 1 mM ethylenediaminetetraacetic acid,
10% glycerol, 1% NP-40, and a cocktail of protease inhibitors). Tissue and cell debris was
removed by centrifugation. The tissue lysate was boiled for 5 min in 1 x SDS sample buffer (50
mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue)
containing 5% β-mercaptoethanol.
Application:
Human lung tumor tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Human Brain Tumor Tissue Lysate
Catalog No: 1322
Source: 75-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human brain tumor (Meningeal tumor) tissue lysate was prepared by homogenization in lysis
buffer (50 mM Tris-HCl pH7.4, 150 mM NaCl, 1 mM PMSF, 1 mM EDTA, 5 µg/ml aprotinin, 5
µg/ml leupeptin, 1% Triton x-100, 1% DOC, 0.1% SDS). Tissue and cell debris was removed by
centrifugation. The tissue lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl
pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-
mercaptoethanol.
Application:
Human brain tumor tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1323
Human Breast Tumor Tissue Lysate
Source: 56-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human breast tumor (moderately differentiated invasive ductal carcinoma) tissue lysate was
prepared by homogenization in lysis buffer (10 mM HEPES pH7.9, 1.5 mM MgCl 2 , 10 mM KCl, 1
mM ethylenediaminetetraacetic acid, 10% glycerol, 1% NP-40, and a cocktail of protease
inhibitors). Tissue and cell debris was removed by centrifugation. The tissue lysate was boiled for
5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium
dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human breast tumor tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1324
Human Kidney Tumor Tissue Lysate
Source: 44-year-old female
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human kidney tumor (renal cell carcinoma) tissue lysate was prepared by homogenization in
lysis buffer (10 mM HEPES pH7.9, 1.5 mM MgCl 2 , 10 mM KCl, 1 mM ethylenediaminetetraacetic
acid, 10% glycerol, 1% NP -40, and a cocktail of protease inhibitors). Tissue and cell debris was
removed by centrifugation. The tissue lysate was boiled for 5 min in 1 x SDS sample buffer (50
mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue)
containing 5% β-mercaptoethanol.
Application:
Human kidney tumor tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1341-N
Human Colon Normal Tissue Lysate
Source: Human adult colon
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human colon normal tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human colon normal tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer
containing 5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1341-T
Human Colon Tumor Tissue Lysate
Source: Human adult colon
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human colon tumor tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human colon tumor tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1342-N
Human Liver Normal Tissue Lysate
Source: Human adult liver
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human liver normal tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human liver normal tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1342-T
Human Liver Tumor Tissue Lysate
Source: Human adult liver
This material has been tested by accepted techniques and has been found to be negative
for HBsAg, HIV 1/2, and HCV.
Tissue lysate preparation:
Human liver tumor tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Human liver tumor tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Heart Tissue Lysate
Catalog No: 1401
Source:
White laboratory mice
Tissue lysate preparation:
Mouse heart tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse heart tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Lung Tissue Lysate
Catalog No: 1402
Source:
White laboratory mice
Tissue lysate preparation:
Mouse lung tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse lung tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Brain Tissue Lysate
Catalog No: 1403
Source:
White laboratory mice
Tissue lysate preparation:
Mouse brain tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse brain tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Liver Tissue Lysate
Catalog No: 1404
Source:
White laboratory mice
Tissue lysate preparation:
Mouse liver tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse liver tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane
is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Kidney Tissue Lysate
Catalog No: 1405
Source:
White laboratory mice
Tissue lysate preparation:
Mouse kidney tissue lysate was prepared by homogenization in modified RIPA buffer (150
mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse kidney tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Mouse Spleen Tissue Lysate
Catalog No: 1406
Source:
White laboratory mice
Tissue lysate preparation:
Mouse spleen tissue lysate was prepared by homogenization in modified RIPA buffer (150
mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse spleen tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1407
Mouse Skeletal Muscle Tissue Lysate
Source:
White laboratory mice
Tissue lysate preparation:
Mouse skeletal muscle tissue lysate was prepared by homogenization in modified RIPA
buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid,
1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse skeletal muscle lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per
lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1408
Mouse Small Intestine Tissue Lysate
Source:
White laboratory mice
Tissue lysate preparation:
Mouse small intestine tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Mouse small intestine tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Heart Tissue Lysate
Catalog No: 1461
Source:
White laboratory rats
Tissue lysate preparation:
Rat heart tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat heart tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Lung Tissue Lysate
Catalog No: 1462
Source:
White laboratory rats
Tissue lysate preparation:
Rat lung tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat lung tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Brain Tissue Lysate
Catalog No: 1463
Source:
White laboratory rats
Tissue lysate preparation:
Rat brain tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat brain tissue lysate is ready to load on SDS -PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
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Rat Liver Tissue Lysate
Catalog No: 1464
Source:
White laboratory rats
Tissue lysate preparation:
Rat liver tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat liver tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Kidney Tissue Lysate
Catalog No: 1465
Source:
White laboratory rats
Tissue lysate preparation:
Rat kidney tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat kidney tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Spleen Tissue Lysate
Catalog No: 1466
Source:
White laboratory rats
Tissue lysate preparation:
Rat spleen tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM
sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat spleen tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg per lane is
recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Catalog No: 1467
Rat Skeletal Muscle Tissue Lysate
Source:
White laboratory rats
Tissue lysate preparation:
Rat skeletal muscle tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat skeletal muscle tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

13100 Kirkham Way
Suite 207
Poway, CA 92064
www.prosci-inc.com
Toll Free: 888-513-9525
Tel: 858-513-2638
Fax: 858-513-2692
techsupport@prosci-inc.com
Rat Small Intestine Tissue Lysate
Catalog No: 1468
Source:
White laboratory rats
Tissue lysate preparation:
Rat small Intestine tissue lysate was prepared by homogenization in modified RIPA buffer
(150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM
phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium
dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Tissue and cell debris was removed by
centrifugation. Protein concentration was determined with Bio-Rad protein assay. The tissue
lysate was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1%
sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% β-mercaptoethanol.
Application:
Rat small Intestine tissue lysate is ready to load on SDS-PAGE for Western blotting, 20 µg
per lane is recommended for mini gel.
Storage:
It is supplied as whole cell lysate at 100 µg at 2 mg/ml in 1 x SDS sample buffer containing
5% β-mercaptoethanol. Store at -20°C for three months or at –70°C for one year.
For research use only.

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Suite 207
Poway, CA 92064
orders@prosci-inc.com
Tel: 858.513.2638
Fax: 858.513.2692
Toll Free: 888.513.9525
www.prosci-inc.com
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PRODUCTS
Catalog No. Description Size Quantity

Protocols

WESTERN BLOT PROCEDURE
1) Load 20 to 25 microgram of whole cell lysate per lane in an SDS-PAGE mini gel.
2) Run at 20 mA per gel untill the dye front is close to the bottom.
3) Transfer the proteins to a nitrocellulose membrane (S&S NCTM) at 250 mA in
transfer buffer for 1-4 h, depending on the size of the target protein.
4) Incubate the blot with blocking buffer (5% non-fat dry milk in TBS) overnight at 4 o C
or 2 h at room temperature (RT).
5) Incubate the blot with primary antibody (diluted 1:250 to 1:1000 in blocking buffer)
for 1 h in blocking buffer at RT.
6) Wash the blot 3 x 10 min in washing buffer (TBS containing 0.1% Tween 20) with
shaking.
7) Incubate blot with anti-rabbit IgG-HRP conjugate (Sigma) (diluted 1:10,000 -
1:2,000 in blocking buffer) for 1 h in blocking buffer at RT.
8) Wash 3 x 10 min in washing buffer with shaking.
9) Drain washing buffer, add ECL solution (Amersham) and develop for 1 min.
10) Expose to X-ray film for 1 to 30 min.
TBS: • 125 mM NaCl
• 25 mM Tris pH 8.0
SDS/Running Buffer: • 25 mM Tris
• 192 mM Glycine
• 1% SDS
Transfer Buffer: • 20 mM Tris pH 8.0
• 150 mM Glycine
• 20% methanol

CELL LYSATE PROCEDURE
1) Wash the cell pellets with ice-cold PBS.
2) Add 1 ml of RIPA buffer per 10 8 cells and incubate on ice for 20 min, vortex 2-3
times, briefly.
3) Aliquat cell lysate into 1.5 ml microfuge tubes and centrifuge at 13,000 rpm, 4 o L for
5 min in an Eppendorf microfuge.
4) Transfer the supernatant into clean tubes. Measure the protein concentration with
BioRad protein assay.
5) Adjust the concentration to 5 mg/ml with RIPA lysis buffer.
6) Add an equal volume of 2 x SDS sample buffer into the cell lysate. Boil for 5 min.
7) Store at -20 o C for daily use or -80 o C for long term storage.
RIPA Buffer: • 50 mM Tris-HCl pH 7.4
• 150 mM NaCl
• 1 mM PMSF
• 1 mM EDTA
• 5 µg/ml Aprotinin
• 5 µg/ml Leupeptin
• 1% Triton -100
• 1% Sodium deoxycholate
• 0.1% SDS
2 x SDS/Sample buffer: • 100 mM Tris
• 25% glycerol
• 2% SDS
• 0.01% bromphenol blue
• Adjust to pH 6.8
• Add 2-ME to 10%