DNA Polymerases
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, Triton free, 1,000U
Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, Triton free. Glycerol free is ideal for automation and free drying applications
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Combination Buffer, Magnesium free and Tween free, 2,500U
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
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, Magnesium free and Triton free, 1,000U
Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, Mg2+ free and Triton free. Glycerol free is ideal for automation and free drying applications
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.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, 500U
Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer. Glycerol free is ideal for automation and free drying applications.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Ammonium Buffer, Magnesium free and Tween free, 10,000U
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.
Cayman Chemical HIghBIndng 96 SolId Pl 5ea
A fluorescent dGTP derivative selectively inhibits recombinant mammalian AC1 AC2 AC5 and AC6 (Kis 260 1200 420 and 470 nM respectively) bovine lung sGC (Ki 220 nM) and B. anthracis edema factor AC toxin (Ki 630 nM) over rat testis sAC and B. pertussis AC toxin (Kis 43 and 14 UM respectively) has been used to study the activity of various GTPases including EF-Tu and H-Ras p21
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Combination Buffer, Tween free, 2,500U
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 tragets. HS Taq Polymerase includes Tween free 10x Combination Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Combination Buffer, 500U
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 tragets. HS Taq Polymerase includes 10x Combination Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Combination Buffer, Magnesium free and Tween free, 500U
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 tragets. HS Taq Polymerase includes Tween/magnesium free 10x Combination Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free, 10x Ammonium Buffer and 10x Standard Buffer both Magnesium free, 5,000U
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 magnesium free 10x Ammonium Buffer and 10x Standard Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Combination Buffer, 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 tragets. HS Taq Polymerase includes 10x Combination Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Combination Buffer, Tween free, 1,000U
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 tragets. HS Taq Polymerase includes Tween free 10x Combination Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer, 2,500U
Taq DNA Polymerase 5 U/ul glycerol free 10x Standard Buffer. Glycerol free is ideal for automation and free drying applications.
Bioworld Firepol (Thermostable TAQ), 1000 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.