can Tris buffer interfere in any way in a NaBH4 trapping assay that is carried out to assess the dRPase activity of a protein? A 5' dRP moeity may react with amine grps in a protein to form a schiffs base. This can be reduced by NaBH4 to form a DNA-protein complex. The reaction buffer will have HEPES as the buffering agent, but the recombinant protein that I am using to assay the 5' dRPase actiivty is stored in a Tris buffer. will this interfere with my assay?