PCR Supplies
Mayflower Bioscience HOT FIREPol DNA Polymerase Kit
Hot-start DNA Polymerase with a unique 30-day stability at room temperature for your everyday PCR needs. A chemically modified hot-start version of the thermostable Taq DNA polymerase FIREPol. This enzyme is activated only by pre-incubation at 95°C, preventing any unspecific polymerase activity at lower temperatures during reaction set-up.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Ammonium Buffer, Magnesium free and Tween free, 2,500U
Taq DNA Polymerase 5 U/ul glycerol free 10x Ammonium Buffer, Mg2+ free and Tween free. Glycerol free is ideal for automation and free drying applications.
Bioworld Firepol (Thermostable TAQ), 4000 Unit(s)
A thermostable DNA polymerase FirePol is similar to Taq DNA polymerase I (homology 98%). 3' to 5' exonuclease activity. Has the "extendase activity", allowing TA cloning. Due to the unique modifications and purification technology it is very thermostable at high temperatures. Can be used in all applications involving polymerase chain reaction (PCR). Contains necessary reaction buffers and MgCl2.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Combination Buffer, Magnesium free and Tween free, 1,000U
Taq DNA Polymerase 5 U/ul glycerol free 10x Combination Buffer, Mg2+ free and Tween free. Glycerol free is ideal for automation and free drying applications
Bioss KD-Validated DNA Polymerase ga
DNA Polymerase Gamma Catalytic Subunit Primary Antibody Unconjugated Public Immunogen Range 20-68/557 Host Species Rabbit Target Species Human Mouse Rat Clonality Monoclonal Applications WB FCM IC Concentration Lot dependent Size 50 ul Storage Buffer Supplied in PBS (pH 7 4) containing 50% glycerol and 0 02% sodium azide
Enzo Life Sciences AMPIGENE Taq Mix (40Reactions)
AMPIGENE Taq Mix uses the latest developments in polymerase technology and buffer chemistry to optimize PCR. The AMPIGENE Taq Mix is a robust mix for routine PCR applications including genotyping, screening, and library construction. An optimized buffer system allows efficient amplification under fast and standard cycling conditions. Applications: PCR.
As One International Inc High Fidelity Taq Polymerase, 10x Ammonium Buffer, Tween free, 1,000U
AS ONE PR Taq DNA Polymerase is a thermostable high fidelity DNA polymerase with proof reading ability. This feature enables accurate and reliable PCR. Besides a 5' to 3' polymerase activity, PR-Taq exhibits a 3' to 5' exonuclease activity that enables the enzyme to correct base pair mismatches. This results in PCR products with very few errors and blunt ends. PR Taq Polymerase includes Tween free 10x Ammonium Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, no buffers, 10,000U
AS ONE HS Taq DNA Polymerase is a hot start polymerase designed to diminish the formation of non-specific priming events during reaction set up and the first ramp of thermal cycling. HS Taq features high specificity and sensitivity, greater yield compared to standard DNA polymerases. HS Taq enables the detection of low abundance targets.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free, 10x Ammonium Buffer and 10x Combination Buffer, 10,000U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Glycerol free Taq is ideal for automation and free drying applications. Included with Taq are 10x Ammonium Buffer and 10x Combination Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer and 10x Combination Buffer, 500U
AS ONE Taq DNA Polymerase with red dye is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. Taq contains a red dye which provides easy and quick identification of reactions to which enzyme was added and allows confirmation of complete mixing. The inert dye has no effect on downstream processes. Taq with Red Dye is added directly to the reaction mix and is used in the same manner as standard Taq DNA Polymerase. AS ONE Taq DNA Polymerase with red dye has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity. Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Red Taq Polymerase includes 10x Ammonium Buffer and 10x Combination Buffer.