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. Author manuscript; available in PMC: 2018 Jan 18.
Published in final edited form as: Protein Expr Purif. 2017 Jan 18;132:68–74. doi: 10.1016/j.pep.2017.01.007

Fig. 1.

Fig. 1

The pCold-I Cold Shock Expression System introduces an N-terminal 6xHis tag followed by a factor Xa cleavage site for tag removal following purification. The gene of interest inserted into the multiple cloning site is under the control of the cspA promoter and lac operon for expression control. The vector imparts ampicillin resistance through the ampr gene encoding β-lactamase.