OGS526

PSF-CMV-RAT-LAMBDA LC - RAT LAMBDA LIGHT CHAIN ANTIBODY VECTOR

plasmid vector for molecular cloning

• 別名: cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector
• NACRES: NA.85
• UNSPSC Code: 12352200
• Promoter: Promoter name: CMV; Promoter activity: constitutive; Promoter type: mammalian
• Origin of replication: pUC (500 copies)
• Bacteria selection: kanamycin
• Reporter gene: none
• Peptide cleavage: no cleavage

特性

• form: buffered aqueous solution
• mol wt: size 4570 bp
• bacteria selection: kanamycin
• origin of replication: pUC (500 copies)
• peptide cleavage: no cleavage
• promoter: Promoter name: CMV; Promoter activity: constitutive; Promoter type: mammalian
• reporter gene: none
• shipped in: ambient
• storage temp.: −20°C

詳細

General description

This cloning plasmid is designed for the production and expression of rat (Rattus rattus) lambda light chain antibody genes. The constant region of the antibody lambda gene has been positioned adjacent to a BseRI restriction site in this plasmid which when cleaved produces an overhang within the first codon of the antibody gene. This allows variable regions of antibodies to be cloned in creating seamless fusion between the the variable and constant regions. As part of this product range we can also provide expression plasmids for both human and mouse antibodies as well as cloning vectors for rat IgG heavy chain and Kappa light chain (pSF-CMV-Rat-IgG HC and pSF-CMV-Rat-Kappa respectively).

Promoter Expression Level: This plasmid contains the mammalian CMV promoter to drive gene expression. We have tested all of our mammalian promoters in a range of cell types and CMV is consistently the strongest in those we have studied. However there are many reports of the CMV promoter demonstrating silencing by methylation in long-term culture.

Application

The plasmid encodes a constant region an antibody in the main multiple cloning site positioned so that it can be cleaved to produce an overhang that allows seamless fusion with a variable region from any antibody. This allows you to create full length antibody genes with no cloning scars.

To enable this immediately upstream of the constant region coding sequence there is a BseRI restriction site. This is a type-IIS restriction enzyme that binds in one position (CAGCAG) and then cleaves a specific number of nucleotides away from the binding site regardless of the sequence at the cleavage point. We use this site in all of our antibody expression cassettes in the same position. In this plasmid cutting with BseRI will result in an overhang consisting of the first two nucleotides of the first codon of the constant region. This means that any variable region with the same overhang at its 3 prime end can be ligated into this plasmid when used in conjunction with any 5 prime site (NotI-NcoI). To add this overhang the variable region must be PCR amplified to contain any of the following sites at its 3 prime end: BseRI BsgI BtsI or BsrDI. By using this system it allows antibody variable regions to PCR amplified and fused to any of our constant region plasmids without having to re-synthesise the entire antibody expression cassette each time.

Analysis Note

To view the Certificate of Analysis for this product, please visit www.oxgene.com

Other Notes

To view sequence information for this product, please visit the product page

安全性情報

• 保管分類: 12 - Non Combustible Liquids
• flash_point_f: Not applicable
• flash_point_c: Not applicable