I have extracted surface proteins from a sample in 2x and 4x DPBS. While preparing standards (BSA) for quantification shall I use the diluent 2x/4x DPBS or mili Q water?
Some reagents such as DPBS or detergents (Triton for instance) interfere with Bradbord assay, so I suggest you to prepare the standards using the same concentration of DPBS you have in your surface proteins sample.