I am using TCA/acetone method to isolate proteins from plant pollen grains. When I suspend the protein pellet in 3% SDS/Tris-HCl buffer, three phases are observed after centrifugation; a pellet at the bottom, an aqueous supernatant in the middle , and a white tiny layer at the top that seems to be lipid.

I have used the aqueous supernatant in the middle to run a gel, and the quality of proteins sound good, but I suspect that some proteins might still be in the lipid phase?!

Any same experience or suggestion, I would appreciate it.

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