DNA Polymerases
Boca Scientific Inc Tth DNA Polymerase, 2500 units
Tth DNA Polymerase is a recombinant, thermostable enzyme with intrinsic reverse transcription (RT) activity. It can be used in both RT-PCR and regular PCR and can reverse transcript and amplify fragments up to 2-3 kb. Tth DNA Polymerase was isolated from eubacterium Thermus thermophilus strain HB8 and is expressed in E.coli. It has a highly processive 5-3 polymerase activity, but no 3-5 exonuclease activity. It also does not have RNase activity.
Boca Scientific Inc Phage T7 DNA, 250ug
Bacteriophage T7 DNA is isolated from an infected E. coli strain. Phage T7 DNA is linear with a length of 39936 bp. T7 DNA is the most popular alternative to Lambda DNA substrate for the restriction endonucleases.
LAMDA BIOTECH INC Taq DNA Polymerase 5000 units
A thermostable enzyme optimized for DNA amplification research applications. Our purified Taq DNA Polymerase is designed for consistent performance in PCR-based molecular biology research.
Takara Bio TaKaRa LA Taq® DNA Polymerase with GC Buffer, 125 units
Takara LA Taq DNA polymerase paired with two special GC-optimized Buffers. This system is designed to amplify templates with up to 73% GC content, and up to 20 kb in length routinely (extension up to 48 kb is possible on some templates). 125 units
Takara Bio TaKaRa LA Taq® DNA Polymerase (Mg2+ free buffer), 125 units
Takara LA Taq is a mixture of Taq Polymerase with a proofreading polymerase. The mixture is optimized for amplification of long DNA templates (routinely 20 kb and up to 48 kb depending on template type) with high fidelity. This LA Taq polymerase mix is supplied with separate tubes of optimized buffer (Mg2+ free), MgCl2, and dNTPs. 125 units
As One International Inc High Fidelity Taq Polymerase, 500U
AS ONE PR Polymerase is a thermostable enzyme with PR ability, which can be used in primer extension reactions and other molecular biology applications. PR Polymerase exhibits both 5 prime to 3 prime DNA polymerase activity and 3 prime to 5 prime PR exonuclease activity. It is recommended for applications, which require extremely high fidelity or blunt ending. Optimal reaction conditions are achieved by using the 10x Ammonium buffer containing MgCl2 provided with the enzyme. 25 mM MgCl2 is also included separately, in case a higher MgCl2 concentration is required for a specific reaction.
As One International Inc Red-Taq DNA Polymerase 2x Master Mix, 2.0 mM MgCl2 (final concentration), 20,000Rxn
AS ONE Taq DNA Polymerase with Red Dye Master Mix is a ready-to-use 2.0x reaction mix. Simply add primers, template, and water to successfully carry out primer extensions and other molecular biology applications. AS ONE Taq Polymerase, the NH4+ buffer system, dNTPs, and magnesium chloride are conveniently present in the Taq DNA Polymerase Mix. An inert red dye and a stabilizer are also present to allow direct loading of the final products onto a gel for analysis. AS ONE Taq DNA Polymerase with Red Dye Mix offers several advantages. Set up time is significantly reduced. There is no need to buy and use separate loading dyes to load reaction products onto agarose gels for electrophoresis and subsequent visualization. The chance of contaminating component stocks is eliminated. Reduction of reagent handling steps leads to better reproducibility. Standard tests can be set up with the confidence that results will be consistent every time.
As One International Inc Taq DNA Polymerase 2x Master Mix, 2.0 mM MgCl2 (final concentration), 2,500Rxn
AS ONE's Taq DNA Polymerase Pre-Mix is a ready-to-use 2.0X reaction mix. Simply add primers, template, and water to successfully carry out primer extensions and other molecular biology applications. AS ONE Taq DNA Polymerase, the NH4+ buffer system, dNTPs, and magnesium chloride are present in Taq DNA Polymerase Mix. Each reaction requires 25 uL of the 2.0X reaction mix. Simply add primers, template and water to a total reaction volume of 50 uL. Taq DNA Polymerase Pre-Mix offers several advantages. Set up time is significantly reduced. The chance of contaminating component stocks is eliminated. Reduction of reagent handling steps leads to better reproducibility. Standard tests can be set up with the confidence that results will be consistent every time.
Bulldog Bio Inc TaqDog Premium DNA Polymerase with 10x Reaction Buffer ( no dNTP), 50,000 Units
TaqDog Premium is a great choice for your everyday PCR needs. This recombinant DNA polymerase is derived from Thermus aquaticus is perfect for 3-step, 2-step, and touchdown protocols, as well as completely compatible with common SYBR™ Green-based qPCR buffers. Each kit includes 10x reaction buffer and is optimized for improved amplification efficiency. Better efficiency allows many protocols to be completed in under 1 hour — that is if your thermal cycler can keep up! TaqDog Premium is also a great enzyme to consider for dramatically reducing the cost of your qPCR experiments. Starting at only a few pennies per unit, its ideal for labs performing mouse tail genotyping, and other high volume PCR processing. The purity of TaqDog Premium is so good, that it’s still 100% fully active after 14 days at 37°C. That’s why we ship it at room temperature — a cost savings for your lab and waste savings for the environment.
Braintree Scientific Accuris Hot Start Taq, DNA Polymerase, 6000u (5u/ul)
Hot Start Taq DNA Polymerase and Master Mix Exceptional sensitivity for low copy PCR Ideal for multiplex PCR and amplification of GC-rich DNA Same enhanced features as Accuris Taq Polymerase Buffer optimized for fast cycling and reproducibility Engineered for controlled polymerase activity, Accuris Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification. When samples are ready, the reaction mixture is heated to 95C to denature the antibody and initiate the reaction. Similar to the standard Accuris Taq, Hot Start Taq is provided with a 5X buffer, or in a ready to use 2X Master Mix. The Master Mix can be ordered with or without a red gel loading dye. Researchers preferring a chemically modified Hot Start polymerase, should order Accuris Hot Start ChemMod. **Sold for research purposes only and not for human use**
Braintree Scientific Accuris Hot Start Master Mix, 2X Taq, 200 x 50ul Reactions
Hot Start Taq DNA Polymerase and Master Mix Exceptional sensitivity for low copy PCR Ideal for multiplex PCR and amplification of GC-rich DNA Same enhanced features as Ac Curis Taq Polymerase Buffer optimized for fast cycling and reproducibility Engineered for controlled polymerase activity, Accuris Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification. When samples are ready, the reaction mixture is heated to 95°C to denature the antibody and initiate the reaction. Similar to the standard Accuris Taq, Hot Start Taq is provided with a 5X buffer, or in a ready to use 2X Master Mix. The Master Mix can be ordered with or without a red gel loading dye. Researchers preferring a chemically modified
Braintree Scientific Accuris Hot Start Master MixRed, 2X Taq, 200 x 50ul React
Hot Start Taq DNA Polymerase and Master Mix Exceptional sensitivity for low copy PCR Ideal for multiplex PCR and amplification of GC-rich DNA Same enhanced features as Ac Curis Taq Polymerase Buffer optimized for fast cycling and reproducibility Engineered for controlled polymerase activity, Accuris Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification. When samples are ready, the reaction mixture is heated to 95°C to denature the antibody and initiate the reaction. Similar to the standard Accuris Taq, Hot Start Taq is provided with a 5X buffer, or in a ready to use 2X Master Mix. The Master Mix can be ordered with or without a red gel loading dye. Researchers preferring a chemically modified
Braintree Scientific Accuris Hot Start Master Mix, 2X Taq, 1000 x 50ul Reactions
Hot Start Taq DNA Polymerase and Master Mix Exceptional sensitivity for low copy PCR Ideal for multiplex PCR and amplification of GC-rich DNA Same enhanced features as Ac Curis Taq Polymerase Buffer optimized for fast cycling and reproducibility Engineered for controlled polymerase activity, Accuris Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification. When samples are ready, the reaction mixture is heated to 95C to denature the antibody and initiate the reaction. Similar to the standard Accuris Taq, Hot Start Taq is provided with a 5X buffer, or in a ready to use 2X Master Mix. The Master Mix can be ordered with or without a red gel loading dye. Researchers preferring a chemically modified **Sold for research purposes only and not for human use**
Braintree Scientific Accuris Hot Start Taq, DNA Polymerase, 500u (5u/ul)
Hot Start Taq DNA Polymerase and Master Mix Exceptional sensitivity for low copy PCR Ideal for multiplex PCR and amplification of GC-rich DNA Same enhanced features as Accuris Taq Polymerase Buffer optimized for fast cycling and reproducibility Engineered for controlled polymerase activity, Accuris Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification. When samples are ready, the reaction mixture is heated to 95C to denature the antibody and initiate the reaction. Similar to the standard Accuris Taq, Hot Start Taq is provided with a 5X buffer, or in a ready to use 2X Master Mix. The Master Mix can be ordered with or without a red gel loading dye. Researchers preferring a chemically modified Hot Start polymerase, should order Accuris Hot Start ChemMod. **Sold for research purposes only and not for human use**