I'm thinking of doing an expt where I fix and X gal stain larvae before 1st
strand cDNA synthesis and PCR. Has anyone tried this? Will the fixing
inhibit the reactions?
My other question about RT PCR is how few larvae could I do it on?
Any help will be greatly appreciated
Dr Claire Russell
Dept of Biochemistry
Tel +171 594 5306
Fax +171 225 0960
e-mail c.russell at ic.ac.uk