Can anyone help me? I'm trying to set up an experiment to
look at genetic diversity within a pop of Drosophila
using PCR illustrated by RAPD analysis. Anyway, I've been
advised to mix a single "reaction cocktail" rather than
lots of seperate ones for each reaction tube.Why?- what
is the advantage of this?
If anyone can help, I'll e-mail them a pint!
BGY6OEB at leeds.ac.Uk