StartingBlock™ T20 (TBS) Blocking Buffer, 1 L - FAQs

View additional product information for StartingBlock™ Blocking Buffer - FAQs (37542, 37543, 37578, 37538X3, 37579, 37538, 37539)

1 product FAQs found

How can I reduce background bands in my Western blot?

Optimize the concentration of primary and secondary antibodies. In some cases, increasing the concentration of blocking agent (BSA or non-fat dry milk) or usiing an alternative blocking solution such as Starting Block or SuperBlock may reduce background signal. After incubation with the primary antibody, wash at least 2 times with TBST (include 0.5 M NaCl in one or more of the wash steps). Avoid Nonidet P40 or Triton X-100 in buffers because protein detection is decreased when these detergents are used.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.