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[Jaaar]

Hi, everyone! I recently encounter a problem in SDS-PAGE for mammallian cell culture medium.

I was doing a transient expression of a target protein (~16kDa) in CHO cell using DMEM+ 10% FBS medium. I collected the culture medium and load 10μl onto 4%-12% Tris-Glycine gel together with Novex Protein Sharp Prestained Standard. During the electrophoresis, I observed that the last three bands of ladder (15kDa, 10kDa and 3 kDa) were packed in a 3mm clear zone across the whole gel. And after staining, there is a big bulk of albumin.

What can i do to remove this bulk of albumin and concentrate my samples without using any kits?

[proteaMatt]

There are chemical depletion methods out there that I believe rely on selective precipitation, but you run the risk of losing non-albumin proteins as well. If your protein of interest is low in abundance, kits are really the way to go.

Edited by proteaMatt, 13 June 2012 - 12:27 PM.