I purified one protein using 3 different columns. The last column I used is Butyl 650M hydrophobic interaction column and I eluted my target protein with 50% propylene glycol. I need to remove propylene glycol and concentrate my elution. I tried to remove it with acetone precipitation, and methanol chloroform precipitation. However, both of them resulted in a significant loss of my protein.
I wonder If I can use dialysis or not...due to its water-absorbing characteristic...
I do not want to add additional steps like gel filtration chromatography...
Does anyone have any technical suggestions and ideas?