I am running PCR products of around 400 bp. The first tests I have done, with a 2% gel have been in an MB agarose. Nothing has appeared. By recommendation I changed to an agarose with low electro-endoosmosis (LE) and suddenly I got a mark in my run.
I can not find the reason why this has happened.
What agarose do you use?
Is there any rule that combines agarose type-genetic material?
Thank you!