02 February 2016 6 5K Report

Hi, I ran two gels yesterday (Beta Actin) and did not get good bands. I am very sure that it has nothing to do with my pipetting (I have ran the same samples before and got good bands), therefore I deduced that it has something to do with the concentration of the primary and secondary antibodies.

Not wanting to waste samples and have not been able to optimize the stripping buffer that we have the lab yet, I decided to reprobe the blots. Is it doable?

Can I reprobe a blot with the same primary antibody that I used earlier? Will that intensify the bands?

Help!

Similar questions and discussions