2-1325-000
                        
                                    
                    
                    pASK-IBA6C vector
                        Periplasmic E. coli expression vector encoding an N-terminal Strep-tag®II, chloramphenicol resistance and protease cleavage site
                    
                
            
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                        pASK-IBA6C is a classic cloning vector devised for E. coli expression of recombinant proteins with the Strep-tag®II fused to the N-terminus. It carries the chloramphenicol resistance cassette for selection of transformed E. coli cells, F1 and ColE1 origin for a high plasmid copy number, a multiple cloning site with recognition sites for several common restriction enzymes (e.g. EcoRI, SmaI, BamHI, SalI, PstI), the inducible tetracycline promoter/operator for the regulated expression of proteins, the ompA signal for periplasmic secretion of the recombinant protein, and the sequence for a protease cleavage site. 
The vector can be combined with any E. coli strain since the tet-promoter works independently of the genetic background of E. coli. Expression of the recombinant protein is induced by addition of anhydrotetracycline, which is a derivative of tetracycline that does not exhibit antibiotic activity. During the secretion into the periplasmic space the ompA signal sequence will be cleaved off. The N-terminal Strep-tag®II can be removed by the protease factor Xa.
                
                                                                The vector can be combined with any E. coli strain since the tet-promoter works independently of the genetic background of E. coli. Expression of the recombinant protein is induced by addition of anhydrotetracycline, which is a derivative of tetracycline that does not exhibit antibiotic activity. During the secretion into the periplasmic space the ompA signal sequence will be cleaved off. The N-terminal Strep-tag®II can be removed by the protease factor Xa.
| Affinity Tag N'-terminal: | Strep-tag®II | 
|---|---|
| Cloning Method: | Direct cloning using e.g. restriction enzyme BsaI in MCS | 
| Concentration: | 250 ng/µl | 
| Expression Host: | E. coli | 
| Form: | Suspension in TE buffer | 
| Possible Application: | Expression plasmid for Strep-tag®II fusion proteins | 
| Promoter: | tet Promoter | 
| Resistance: | Chloramphenicol | 
| Sequence: | See Documents | 
| Size: | 3081 bp | 
| Specificity: | Factor Xa cleavage site | 
| Storage: | -20 °C | 
|---|---|
| Stability: | 12 months after shipping | 
| Shipping: | Room temperature |