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[greenappleap]

I purified a MBP-tagged protein, which is quited soluble. On SDS-PAGE, the MW is  about 65 KDa and it's a very thick band. However,  when I run the protein elution on gel filtration, both 75 and 200 column, there is no any peak for protein. The running buffer I used is the same as elution buffer for purification.
I really don't know what happened? Did my protein degraded or it's stucked on the column?

Thanks for your help! I am really frustrated about this.

Sophia

[leekaming]

Are you confident in the loading procedure of gel filtration?
in my lab, some labmate load the protein wrongly and result in loss of all protein