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2012 Promega catalogue

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Cell Signaling<br />

pSP64 Poly(A) Vector<br />

Product Size Cat.# Price ($)<br />

pSP64 Poly(A) Vector 20 µg P1241 161.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

Description: The pSP64 Poly(A) Vector can be used as a standard cloning<br />

vector and for in vitro transcription from the SP6 promoter. The pSP64 Poly(A)<br />

Vector also can be used to generate poly(A)+ transcripts in vitro. The vector<br />

has a stretch of 30 dA:dT residues inserted between the SacI and EcoRI sites.<br />

Therefore, when foreign DNA is cloned into any polylinker site other than EcoRI<br />

(HindIII, PstI, SalI, AccI, HincII, XbaI, BamHI, AvaI, SmaI or SacI), linearization of<br />

the recombinant plasmid with EcoRI allows the use of SP6 RNA polymerase in<br />

vitro to prepare RNA copies of the inserted sequences that contain a synthetic<br />

3´ “poly(A)” tail of 30 residues.<br />

Features:<br />

• In Vitro Transcription: The SP6 promoter is next to the polylinker.<br />

• Generates Poly(A)+ Transcripts In Vitro: A stretch of 30 dA:dT<br />

residues are inserted between the SacI and EcoRI sites in the polylinker.<br />

Poly(A) tails can stabilize RNAs and lead to greater yields for in vitro<br />

translation reactions.<br />

• Convenient: Multiple cloning region provides a selection of restriction<br />

sites for cloning.<br />

Storage Conditions: Store vector at –20°C.<br />

Protocol Part#<br />

pSP64 Poly(A) Vector Technical Bulletin TB052<br />

ScaI<br />

1814<br />

PvuI<br />

1704<br />

FspI<br />

1556<br />

BglI<br />

1454<br />

SspI 2138<br />

XmnI 1933<br />

Amp r<br />

AatII 2256<br />

pSP64 Poly(A)<br />

Vector<br />

(3,030bp)<br />

ori<br />

SphI 2599<br />

NaeI 2758<br />

NheI 2789<br />

PvuII<br />

265<br />

HindIII<br />

PstI<br />

SalI<br />

AccI<br />

HincII<br />

XbaI<br />

BamHI<br />

AvaI<br />

SmaI<br />

SacI<br />

(dA:dT) 30<br />

EcoRI<br />

For complete and up-to-date product information visit: www.promega.com/catalog<br />

SP6<br />

➞<br />

1 start<br />

7<br />

20<br />

22<br />

23<br />

24<br />

28<br />

34<br />

39<br />

41<br />

50<br />

86<br />

0306VA05_2A<br />

pSP72 Vector<br />

Product Size Cat.# Price ($)<br />

pSP72 Vector<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

20 µg P2191 143.00<br />

Description: The pSP72 Vector can be used as a standard cloning vector and<br />

also can be used for transcription of RNA in vitro. The pSP72 Vector contains<br />

the SP6 and T7 RNA polymerase promoters flanking a unique multiple cloning<br />

region, which includes restriction sites for XhoI, PvuII, HindIII, SphI, PstI, SalI,<br />

AccI, XbaI, BamHI, SmaI, KpnI, SacI, EcoRI, ClaI, EcoRV and BglII. The pSP72<br />

and pSP73 Vectors are essentially identical except for the orientation of the<br />

multiple cloning site region.<br />

Features:<br />

• Versatile: This vector can be used for standard cloning and in vitro transcription<br />

from SP6 and T7 RNA polymerase promoters flanking the multiple<br />

cloning region.<br />

• Convenient: Multiple cloning site provides a selection of restriction sites<br />

for cloning.<br />

Storage Conditions: Store vector at –20°C.<br />

Protocol Part#<br />

pSP72 Vector Technical Bulletin TB040<br />

PvuI 1578 AatII 2130<br />

Amp<br />

pSP72<br />

Vector<br />

(2,462bp)<br />

r<br />

XmnI 1807<br />

ScaI 1688<br />

SspI <strong>2012</strong><br />

FspI<br />

430<br />

BglI<br />

1328<br />

NdeI<br />

2379<br />

ori<br />

HpaI<br />

136<br />

SP6<br />

XhoI<br />

PvuII<br />

HindIII<br />

SphI<br />

PstI<br />

SalI<br />

AccI<br />

XbaI<br />

BamHI<br />

SmaI<br />

KpnI<br />

SacI<br />

EcoRI<br />

ClaI<br />

EcoRV<br />

BglII<br />

T7<br />

➞➞<br />

1 start<br />

4<br />

12<br />

16<br />

26<br />

32<br />

34<br />

35<br />

40<br />

46<br />

53<br />

59<br />

65<br />

67<br />

74<br />

81<br />

85<br />

101<br />

0298VA05_2A<br />

103<br />

4<br />

Cloning and DNA Markers<br />

Section<br />

Contents<br />

Table of<br />

Contents

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