Hi everyone!
I am currently trying to quantify ApoB in VLDL samples (isolated from plasma by density gradient ultracentrifugation) using Western Blot analysis. Unfortunately, I only see blurred bands, maybe because of the high triglyceride content.
Does anyone know how to get sharp bands? Should I delipidate the samples prior to gel electropheresis? If yes, what is the best way to do it? Is it possible to use Folch extraction?
Thanks in advance!
Kind regards,
Matthäus Metz