Document Finishing by Wordzworth
Document Finishing by Wordzworth
Document Finishing by Wordzworth
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CATALOG<br />
NUMBER<br />
BOC-ASP(OMe)-FMK<br />
-20 TO 0°C<br />
FK011<br />
BOC-GLN-GLY-ARG-7-AMINO-4-<br />
TRIFLUOROMETHYLCOUMARIN<br />
RT<br />
AFC137<br />
N-t-BOC-L-GLUTAMIC ACID -t-BUTYL ESTER<br />
Biochemicals<br />
Alphabetical List<br />
1 mg<br />
3 mg<br />
5 mg<br />
10 mg<br />
C14H25NO6<br />
0°C MW 303.4 13726-84-6<br />
199052 5 g<br />
N--t-BOC-GLYCINE<br />
C7H13NO4<br />
0°C MW 175.2 4530-20-5<br />
101071 25 g<br />
N--t-BOC-L-HISTIDINE<br />
Crystalline<br />
C11H17N3O4<br />
0°C MW 255.3 17791-52-5<br />
150496 5 g<br />
BOC-LEU-ARG-ARG-7-AMINO-4-METHYLCOUMARIN<br />
RT<br />
AMC113<br />
N--t-BOC-L-METHIONINE<br />
Free Acid<br />
Crystalline<br />
C10H19NO4S<br />
0°C MW 249.3 2488-15-45<br />
104916<br />
N-t-BOC-PHE-LEU-PHE-LEU-PHE<br />
A chemotactic peptide antagonist.<br />
A competitive antagonist of the binding of N-formyl-Met-Leu-Phe to<br />
neutrophils.<br />
Ref.: 1. O’Dea, R.F., et al., Nature, 272: 462, (1978); 2. Naccache, P., et<br />
al., Science, 203: 461, (1979); 3. Freer, R.J., et al., Peptides, 1: 289,<br />
(1980).<br />
C44H59N5O8<br />
10 mg<br />
25 mg<br />
N-t-BOC-MET-LEU-PHE<br />
A chemotactic peptide antagonist.<br />
Ref: Freer, R.J., Gross, E. and Meienhofer, J., eds., et al., Peptides,<br />
Structure and Biological Function, Proceedings of the Sixth<br />
American Peptide Symposium, 749, (1979).<br />
C25H39N3O6S<br />
1 g<br />
-20 TO 0°C MW 509.7 67247-12-5<br />
152799 5 mg<br />
25 mg<br />
100 mg<br />
-20 TO 0°C MW 786 73572-58-4<br />
152760 5 mg<br />
CATALOG<br />
NUMBER<br />
C10H17NO4<br />
15761-39-4<br />
101092 25 g<br />
N--t-BOC-L-SERINE<br />
BOC-VAL-ILE[(S)-4-AMINO-2,2-DIFLUORO-3-OXO-<br />
PENTANOYL]-VAL-ILE-OME<br />
RT<br />
DFK167<br />
1 mg<br />
3 mg<br />
BOMBESIN<br />
(pyroGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2)<br />
A tetradecapeptide that has biological activities in the central nervous<br />
system and gastrointestinal tract; also has thermoregulatory effects.<br />
Ref.: 1. Bertaccini, G., et al., Br. J. Pharmac., 52: 219, (1974); 2.<br />
Erspamer, V., et al., Br. J. Pharmac., 52: 227, (1974); 3. Rivier, J.E. and<br />
Brown, M.R., Biochemistry, 17: 1776, (1978).<br />
C71H110N24O18S<br />
-20 TO 0°C MW 1619.9 31362-50-2<br />
190307<br />
www.mpbio.com<br />
N--t-BOC-L-<br />
Free Acid<br />
Crystalline<br />
C14H19NO4<br />
0°C MW 265.3 13734-34-4<br />
101090 25 g<br />
N--t-BOC-L-PHE-L-SER-L-ARG-4-<br />
METHYLCOUMARYL-7-AMIDE<br />
Fluorogenic substrate for trypsin<br />
C33H43N7O8<br />
0°C MW 665.8 73554-90-2<br />
150505<br />
N--t-BOC-L-<br />
PROLINE<br />
Crystalline<br />
Crystalline<br />
C8H15NO5<br />
0°C MW 205.2<br />
101093<br />
N--t-BOC-L-TYROSINE<br />
Crystalline<br />
C14H19NO5<br />
0°C MW 281.3<br />
101054<br />
BORAX<br />
(Sodium tetraborate)<br />
Purity: ~99%<br />
Used as a buffer<br />
pH in solution approx. 9.3<br />
B4Na2O7 • 10H2O<br />
3262-72-4<br />
3978-80-1<br />
5 mg<br />
1 g<br />
5 g<br />
RT MW 381.4 1303-96-4<br />
190308 500 g<br />
1 kg<br />
5 kg<br />
5 g<br />
1 mg<br />
102<br />
One Call. One Source. A World of Biotechnology Reagents. www.mpbio.com
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