Atlas HotTaq DNA Polymerase
– Polymerase chain reaction setup at room temperature.
– Effective incorporation of modified nucleotides.
Atlas HotTaq DNA Polymerase catalyzes 5´ to 3´synthesis of DNA. The enzyme has been proved not having the 3´ to 5´ exonuclease activity. Prior the first PCR step the Atlas HotTaq DNA Polymerase should be activated by 15 minute incubation at 95-97°C.
Concentration: 10 units/µl
Unit definition: One unit of the enzyme catalyzes the incorporation of 10 nanomoles of deoxyribonucleotides into a polynucleotide fraction in 30 min at 70°C.
Source: Recombinant E. coli strain with cloned gene encoding Thermus aquaticus DNA polymerase.
Quality control: Free of detectable, non-specific nucleases. Activity and stability tested at 20, 30 and 40 cycles of PCR reaction at 95°C. Tested for the absence of human DNA contamination by PCR with Alu-specific primers.
Atlas 10x Taq Buffer: 100 mM Tris-HCl (pH 8.8 at 25°C), 500 mM KCl, 0.8% Nonident P40.
Atlas 10x Taq Buffer with (NH4)2SO4: 750 mM Tris-HCl (pH 8.8 at 25°C),
200 mM (NH4)2SO4, 0.1% Tween 20.
Atlas 25 mM MgCl2
Storage conditions: 20 mM Tris-HCl (pH 8.0), 1 mM DTT, 0.1 mM EDTA, 100 mM KCl, 0.5% Nonidet P40, 0.5% Tween 20 and 50% glycerol. Store at -20°C. Guaranteed stable for 12 months when properly stored.
Comments: This product is supplied for research use only.
|Product||Quantity||Cat. #||Data Sheet||MSDS|
|Atlas HotTaq DNA Polymerase||500 units||BA00203|
|Atlas HotTaq DNA Polymerase||1000 units||BA00204|
|Atlas HotTaq DNA Polymerase||2500 units||BA00205|