In article <ZEbuQGAvkk72Ew7o at genesys.demon.co.uk>, "Dr. Duncan Clark" <Duncan at genesys.demon.co.uk> wrote: > In article <7ck8d8$s22$1 at nnrp1.dejanews.com>, ladasky at my-dejanews.com > writes > > > >The long PCR protocols typically use between 1% and 10% Taq polymerase in > >conjunction with Vent (NEB) or Pwo (Boehringer) or Pfu (Stratagene). This > >way you get the error correction of the high-fidelity enzym and the proces- > >sivity of Taq. >> Wrong way around. 1-10% proof-reading to 90-99% Taq. >> Duncan > -- > The problem with being on the cutting edge is that you occasionally get > sliced from time to time.... Whoops! Of course you're right. And today, I got sliced! -----------== Posted via Deja News, The Discussion Network ==---------- http://www.dejanews.com/ Search, Read, Discuss, or Start Your Own