I used to use buffer with 1% NP-40, 50mM Hepes and 150mM NaCl as my lysis buffer when analyzing Src protein abundance with my samples. Since c-Src is a membrane anchored protein, I am wondering if I should add some more detergent, like 0.1% SDS or something more, to better solubilize this protein.
Does any one of you have experience on this? Thanks for your recommendations.