I'm trying to plot a protein calibration curve using BSA (fraction V) standards and from what I read so far it seems that a lot of lysis buffers contain detergents which react with Bradford reagent at certain concentrations. Pretty much all of the buffers I came across have a detergent concentration which exceeds the threshold stipulated by product sheet supplied by Sigma for the Reagent.
I'm looking for a way to work around this problem since I have no other reagents at my disposal.