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Description
The pLSG-IBAwt1 vector carries the Polyhedrin promoter for high-level expression in insect cells.
- Co-transfection with BacPAK6 linearized AcMNPV DNA (Clontech) or circular flashBAC modified AcMNPV DNA (Oxford Expression Technologies) allows the generation of recombinant baculovirus at very high efficiency through reconstitution of an essential gene (ORF 1629) and elimination of wild type virus to great extent.
- Cloning and expression of recombinant proteins in insect cells
- Polyhedrin promoter drives high-level expression of the insert
- Ampicillin resistance and ColE1 origin of replication (pUC) support propagation in E. coli
Please note that cloning into pLSG-IBA Acceptor Vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pLSG-IBA vectors with Esp3I, another option via a so-called Entry-Vector is possible.
Specifications
Specifications
| Format | Liquid |
| For Use With (Equipment) | StarGate™ System, Insect Host Cells |
| Inducing Agent | BacPAK6 linearized A cmNPV DNA (Clontech) or circular flashBAC modified A cmNPV DNA (Oxford Expression Technologies) |
| Includes | pUC ori, Ampicillin resistance |
| pH | 8 |
| Promoter | Polyhedrin |
| Product Type | Acceptor Vector for bacula (insect cell) expression |
| Storage Buffer | 20 μL TE buffer: 10 mm Tris-HCl, 1 mm EDTA / 5 μg |
| Content And Storage | 2°C to 8°C for frequent usage, -20°C for long-term storage |
| Protein Tag | Untagged |
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