Adds a C terminal FLAG tag (frame 3) to a gene inserted into our main multiple cloning site. Also contains the CMV promoter to drive transcription.
Product Name: pSF-CMV-COOH-FLAG3
Product Code: OG55
Size (bp): 4252 bp
Bacterial Antibiotic Selection: KanR
Origin and Compatibility: pUC high copy derived from pBR322
Bacterial Copy Number: 500-700 per cell
Promoter: Cytomegalovirus (CMV) immediate early promoter
This vector adds a FLAG tag that allows protein detection or purification using antibodies against the peptide. The FLAG tag will be positioned at the 3 prime end (C terminus) of a gene (expressed protein) in the primary MCS (NotI to XbaI). The FLAG tag coding sequence is DYKDDDDK. This sequence contains an enterokinase cleavage sequence (DDDDK) however when used as a C terminal tag this will not remove the tag because it cleaves after the final lysine.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. For this reason we stock a range of other promoters that are compatible with this plasmid and are available on request.
FLAG is a registered trademark of the Sigma Aldrich Corporation.
This plasmid contains three alternative transcription terminators for mammalian bacterial and bacteriophage (T7) expression. This means that only the promoter needs to be changed to alter the expression system you are using. We sell multiple promoters that can be used in each of these systems. The presence of each terminator does not reduce expression in the alternative systems.
There is a start codon in the NcoI site can be removed by digestion with KpnI if required. The MCS for gene insertions extends from NotI to XbaI. There are built in Shine-Dalgarno and KOZAK sequences aligned with the start codon within the NcoI restriction site. If these are removed you will need to add a ribosomal entry site to the 5 prime end of your gene for optimal expression.