pGEX-KT
pGEX-KT
规格:
货期:
编号:TS163361
品牌:Testobio
| 产品名称： | pGEX-KT |
|---|---|
| 商品货号： | TS163361 |
| Designations： | pGEX-KT |
| Depositors： | DJ Hakes, JE Dixon |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 4.9840002059936520 Vector: pGEX-KT (plasmid) Promoters: Promoter tac Construction: pGEX-1 Marker(s):ampR Construct size (kb): 4.984000205993652 Features: marker(s): ampR other: thrombin cleavage site promoter: tac replicon: pMB1 repressor gene: lacIq MCS: BamHI SmaI EcoRI epitope tag: GST |
| Applications： | encodes an epitope tag for protein isolation or monitoring expression vector vector permitting construction of fusion proteins |
| Comments： | Restriction digests of the clone give the following sizes (kb): BamHI--5.0; EcoRI/PstI--4.0, 1.0; EcoRI/EcoRV--3.2, 1.8. The resulting protein contains two additional amino acids at the amino terminus (Gly-Ser). Expression vector for rapid purification of fusion proteins and release of proteins with fewer extraneous N-terminal amino acids. The glutathione S-transferase (GST) fusion protein can be purified by glutathione affinity chromatography, and the desired polypeptide released from the fusion product by thrombin. Constructed from pGEX-1 by inserting an oligonucleotide at the BamHI site which encodes the glycine "kinker" and thrombin recognition site to enhance cleavage of the fusion protein. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Hakes DJ, Dixon JE. New vectors for high level expression of recombinant proteins in bacteria. Anal. Biochem. 202: 293-298, 1992. PubMed: 1519755 |
| Shipped： | freeze-dried |
| Shipping Information： | Freeze dried E. coli containing the plasmid |
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| 产品名称： | pGEX-KT |
|---|---|
| 商品货号： | TS163361 |
| Designations： | pGEX-KT |
| Depositors： | DJ Hakes, JE Dixon |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 4.9840002059936520 Vector: pGEX-KT (plasmid) Promoters: Promoter tac Construction: pGEX-1 Marker(s):ampR Construct size (kb): 4.984000205993652 Features: marker(s): ampR other: thrombin cleavage site promoter: tac replicon: pMB1 repressor gene: lacIq MCS: BamHI SmaI EcoRI epitope tag: GST |
| Applications： | encodes an epitope tag for protein isolation or monitoring expression vector vector permitting construction of fusion proteins |
| Comments： | Restriction digests of the clone give the following sizes (kb): BamHI--5.0; EcoRI/PstI--4.0, 1.0; EcoRI/EcoRV--3.2, 1.8. The resulting protein contains two additional amino acids at the amino terminus (Gly-Ser). Expression vector for rapid purification of fusion proteins and release of proteins with fewer extraneous N-terminal amino acids. The glutathione S-transferase (GST) fusion protein can be purified by glutathione affinity chromatography, and the desired polypeptide released from the fusion product by thrombin. Constructed from pGEX-1 by inserting an oligonucleotide at the BamHI site which encodes the glycine "kinker" and thrombin recognition site to enhance cleavage of the fusion protein. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Hakes DJ, Dixon JE. New vectors for high level expression of recombinant proteins in bacteria. Anal. Biochem. 202: 293-298, 1992. PubMed: 1519755 |
| Shipped： | freeze-dried |
| Shipping Information： | Freeze dried E. coli containing the plasmid |
