PCR
First generation Pfu polymerases, such as cloned Pfu, PfuTurbo, and PfuUltra, have been improved upon. The improved products, PfuUltra II and Herculase II provide all the benefits of the first generation enzymes plus additional features such as speed to results and larger amplicons. Cloned Pfu DNA Polymerases First generation PfuUltra DNA Polymerases PfuTurbo DNA Polymerases
First generation Pfu polymerases, such as cloned Pfu, PfuTurbo, and PfuUltra, have been improved upon. The improved products, PfuUltra II and Herculase II provide all the benefits of the first generation enzymes plus additional features such as speed to results and larger amplicons. Cloned Pfu DNA Polymerases First generation PfuUltra DNA Polymerases PfuTurbo DNA Polymerases
First generation Pfu polymerases, such as cloned Pfu, PfuTurbo, and PfuUltra, have been improved upon. The improved products, PfuUltra II and Herculase II provide all the benefits of the first generation enzymes plus additional features such as speed to results and larger amplicons. Cloned Pfu DNA Polymerases First generation PfuUltra DNA Polymerases PfuTurbo DNA Polymerases
The engineered PfuUltra II Fusion HS DNA Polymerase provides the worlds most accurate copies and the fastest extension times possible. PfuUltra II Fusion HS DNA Polymerase is PfuUltra hotstart DNA polymerase coupled with a fusion polymerase technology and ArchaeMaxx PCR enhancing factor. The industry standard for ultra high fidelity PCR providing the most accurate copies of DNA Dramatically reduced extension times allow f…
SP6 RNA Polymerase is a DNA-dependent RNA polymerase with high sequence specificity for SP6 promoter sequences. SP6 RNA polymerase synthesizes RNA 5' to 3' and incorporates 35S, 32P and 33P ribonucleotides. This enzyme is isolated from an overproducing recombinant E. coli clone.
SureStart Taq DNA polymerase is a hot start Taq DNA polymerase. SureStart Taq can be incorporated into PCR protocols previously optimized with Taq DNA polymerase, with little or no modification of cycling parameters or reaction conditions.
Bacteriophage T3 and T7 RNA polymerases are DNA-dependent RNA polymerases with high sequence specificity for T3 or T7 promoters.
T4 DNA ligase catalyzes the linkage of adjacent 5'-phosphate and 3'-hydroxy ends of double-stranded DNA by formation of a phosphodiester bond. It is used to ligate cohesive ends in an overnight reaction. The enzyme efficiently joins both blunt and cohesive ends and repairs single stranded nicks in duplex DNA, RNA or DNA/RNA hybrids.
Bacteriophage T3 and T7 RNA polymerases are DNA-dependent RNA polymerases with high sequence specificity for T3 or T7 promoters.
Taq2000 DNA Polymerase is a highly purified, recombinant Taq DNA polymerase cloned from the thermophilic eubacteria, Thermus aquaticus.
