PCR Equipment and Supplies
Meridian Life Science Taq HS DNA Polymerase, 10ML
Taq HS DNA Polymerase is an antibody-mediated hot-start DNA polymerase provided with an optimized buffer system containing dNTP, MgCl2, stabilizers, and PCR enhancers at optimal concentrations which eliminates the need for optimization. The DNA polymerase has been developed to give more robust amplification than other polymerases allowing it to perform well with challenging templates in the presence of PCR inhibitors, making it ideal for fast PCR reactions across a range of templates, without compromising specificity or yield.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Combination Buffer, Magnesium free, 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. Included with Taq is magnesium free 10x Combination Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Standard Buffer, Magnesium free and Triton free, 5,000U
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 Triton/magnesium free 10x Standard Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Ammonium Buffer and 10x Combination Buffer both Magnesium free, 1,000U
AS ONE HS DNA Polymerase is a modified form of AS ONE Taq DNA Polymerase, which is activated by heat treatment. A chemical moiety is attached to the enzyme at the active site, which renders the enzyme inactive at room temperature. Thus, during setup and the first ramp of thermal cycling, the enzyme is not active and misprimed primers are not extended. The result is higher specificity and greater yields when compared to standard DNA polymerases. Once the reaction reaches optimal activating temperature, the chemical moiety is cleaved during a 15 minute heat activation step, releasing the active HS Polymerase DNA Polymerase into the reaction. HS Taq includes magnesium free 10x Ammonium Buffer and 10x Combination Buffer
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Ammonium 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 targets. HS Taq Polymerase includes10x Ammonium Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer, Tween free, 1,000U
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 Tween free 10x Ammonium Buffer.
KYINNO BIOTECHNOLOGY (BOSTON) INC BHK21-T7-RNA-POLYMERASE-CELL-L
NC3866885 BHK21-T7-RNA-POLYMERASE-CELL-L
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free, 10x Ammonium Buffer and 10x Standard Buffer, 2,500U
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 Standard Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer, Magnesium free and Tween free, 10,000U
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 Tween/magnesium free 10x Ammonium Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer and 10x Combination Buffer both Magnesium free, 5,000U
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 magnesium free 10x Ammonium Buffer and 10x Combination Buffer.
INTACT GENOMICS INC Bsu DNA Polymerase Large Fragment, Glycerol Free 200 Units (5 units/µl)
Glycerol Free Bsu DNA Polymerase I, Large Fragment is suitable for various purposes including RPA (Recombinase Polymerase Amplification).Bsu DNA Polymerase I, Large Fragment is a product of the Bacillus subtilis DNA polymerase I which lacks the N-terminal exonuclease domain (1-296 amino acids). It retains the 5´→ 3´ polymerase activity of DNA polymerase I but lacks the 5´→ 3´ exonuclease activity. This large fragment also lacks 3´→ 5´ exonuclease activity.
Meridian Life Science Low DNA Taq HS Poly 5 U/uL, 10ML
Low DNA Taq HS, 5 U/uL is a highly purified chemically modified hot start Taq DNA polymerase and buffer system, with separate magnesium. It is inactive at ambient temperature, avoiding extension of non-specifically annealed primers or primer dimers and providing higher specificity of DNA amplification. Low DNA Taq HS, 5 U/uL catalyzes 5′-3′ synthesis and possesses low 5′-3′ exonuclease activity, however these are not detectable before activation, enhancing PCR sensitivity. The functional activity of the enzyme is restored during a 10-minute incubation at 95 C. The low DNA background and stringent hot-start properties of Low DNA Taq HS, 5 U/uL are ideal for PCR of low-copy bacterial targets and avoiding false-positive amplification, such as in water testing.