Hi
I express some flag and 6his tag exogenous genes in CHO cells and I need to quantify thier expression in different clones so I am going to coat my cell lysate on 96 well plates and do elise with anti tag antibody, but since tags are very small in comparision to whole cellular proteins I am not sure if it really works, I know I can use sandwich elisa in which antibodies against expressed proteins are coated on plates but it seems very expensive for my project.
is there any suggestion?
setting an leisa for quantification of recombinant protein
Started by sara.r, Jan 28 2010 06:45 AM
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