missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Please login to your online account to display your discounted pricing
Promega pGEM™ Vectors 
Enable blue/white screening and contain both the SP6 and T7 RNA polymerase promoters
$182.95 - $234.27
Specifications
| Promoter | SP6, T7 |
|---|---|
| Content And Storage | -30°C to -10°C |
| Quantity | 20 μg |
| For Use With (Application) | Synthesis of RNA in-vitro and allows selection of recombinants by blue/white screening |
| Catalog Number | Mfr. No. | Restriction Site | Vector | Price | Quantity | ||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Restriction Site | Vector | Price | Quantity | ||||
|
PR-P2271
|
Promega
P2271 |
EcoRI, SacI, KpnI, AvaI, SmaI, BamHI, XbaI, SalI, AccI, HincII, PstI, SphI and HindIII | pGEM-3Zf(+) vector |
Each for $184.25
|
|
||||
|
PR-P2261
|
Promega
P2261 |
EcoRI, SacI, KpnI, AvaI, SmaI, BamHI, XbaI, SalI, AccI, HincII, PstI, SphI and HindIII | pGEM-3Zf(-) vector |
Each for $182.95
|
|
||||
|
PR-P2241
|
Promega
P2241 |
ApaI, AatII, SphI, NcoI, SacII, EcoRV, SpeI, NotI, PstI, SalI, NdeI, SacI, BstXI and NsiI | pGEM-5Zf(+) vector |
Each for $234.27
|
|
||||
|
PR-P2251
|
Promega
P2251 |
ApaI, AatII, SphI, XbaI, XhoI, EcoRI, KpnI, SmaI, ClaI, HindIII, BamHI, SacI, BstXI and NsiI | pGEM-7Zf(+) vector |
Each for $234.27
|
|
||||
|
PR-P2151
|
Promega
P2151 |
Acc I, Ava I, BamH I, EcoRI, Hinc II, Hind III, Kpn I, Pst I, Sac I, Sal I, Sma I, Sph I, Xba I, Xma I | pGEM-3Z vector |
Each for $184.25
|
|
||||
Description
- Multiple cloning site provides a selection of restriction sites and is flanked by the SP6 and T7 RNA polymerase promoters
- lacZ α-peptide and multiple cloning site arrangement from pUC18 allow recombinants to be selected using blue/white screening
- Versatile vectors can be used for standard cloning and in vitro transcription
- pGEM-3Z and pGEM-4Z vectors are identical except for the orientation of the SP6 and T7 promoters
- Vectors are derived from the pGEM-3Z vector and contain the origin of replication of the filamentous phage f1
- Versatile vectors can be used for standard cloning, ssDNA production, and in vitro transcription
- (+) and (-) vectors with the same numeric designation are identical except for the orientation of the f1 origin
- pGEM-5Zf(+/-) and -7Zf(+/-) contain restriction site arrangements designed to generate unidirectional deletions with the Erase-a-Base™ System
- pGEM-9Zf(-) permits the excision of an insert containing the SP6 and T7 polymerase promoters
Specifications
| SP6, T7 | |
| -30°C to -10°C | |
| 20 μg | |
| Synthesis of RNA in-vitro and allows selection of recombinants by blue/white screening |