I have always been told that a biotin conjugated primary antibody followed by a fluorescent conjugated streptavidin secondary antibody is a method that should make a low density signal more bright. Is this really true or just theoretical? I ask this question because when I have performed comparisons between direct and indirect staining methods I have never seen much difference. Thanks, Jeffrey
This archive was generated by hypermail 2b29 : Sat Mar 10 2001 - 19:31:08 EST