I purify my protein but in SDS-PAGE gel I have two proteins ( my protein and DNAk). I cant separate with Size exclusion column so I supposed both proteins are attached. So I want separated my protein of DNAk. How could do?. Thank you
As Dominique said, you can do a chaperone wash(buffer containing ATP) before elution of your protein. I normally do not get chaperone contamination after washing the column with chaperone buffer. In cases, when it is difficult to remove chaperones from my protein, I would go for ion exchange.