In article <01H270UZ8NJK002FUD at DUCVAX.AUBURN.EDU>
TEMANUL at DUCVAX.AUBURN.EDU writes:
> I will try to amplify a 2 kb genomic DNA fragment using 25mer primers
> (mp= 60 C, 100 % homology) Has anybody experience and can give me
> optimal or standard conditions for the PCR (DNA/primer concentration,
> reaction temperatures/time) to start? Thanks, Gela.
I've mailed you the FAQ list which is a good place to start.
In there you will find a list of good reviews and books for
optimizing your PCR reactions.
Paul N. Hengen
National Cancer Institute
Frederick Cancer Research and Development Center
Frederick, Maryland 21702-1201 USA