Science, Volume 292John Michels (Journalist) American Association for the Advancement of Science, 2001 |
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Page 1598
... Polymerase Excels in Amplifying Difficult Targets Herculase +/- DMSO ( % ) 0 6 7 8 9 0 Competitor's GC - Rich System +/- GC - RICH solution ( M ) 0.5 1.0 1.5 2.0 M 1 2 3 4 5 6 7 8 9 10 HERCULASE DNA polymerase easily amplifies an 82.5 ...
... Polymerase Excels in Amplifying Difficult Targets Herculase +/- DMSO ( % ) 0 6 7 8 9 0 Competitor's GC - Rich System +/- GC - RICH solution ( M ) 0.5 1.0 1.5 2.0 M 1 2 3 4 5 6 7 8 9 10 HERCULASE DNA polymerase easily amplifies an 82.5 ...
Page 1786
... POLYMERASE Version Available ! Why risk getting the wrong PCR clone ? Even with a 1 kb target , Taq introduces significantly more errors than PfuTurbo DNA polymerase ** , often resulting in the wrong clone . Using PfuTurbo DNA polymerase ...
... POLYMERASE Version Available ! Why risk getting the wrong PCR clone ? Even with a 1 kb target , Taq introduces significantly more errors than PfuTurbo DNA polymerase ** , often resulting in the wrong clone . Using PfuTurbo DNA polymerase ...
Page 1845
... polymerase ( 2 ) presented even more diffi- culties because even highly purified preparations contained many inactive Mg 2+ Synthesis Pre - translocation Bridge helix NTP only of polymerase II itself , but also of the related bacterial ...
... polymerase ( 2 ) presented even more diffi- culties because even highly purified preparations contained many inactive Mg 2+ Synthesis Pre - translocation Bridge helix NTP only of polymerase II itself , but also of the related bacterial ...
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