DNA Polymerases
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free 10x Ammonium Buffer, Magnesium free, 10,000U
Taq DNA Polymerase 5 U/ul glycerol free 10x Ammonium Buffer, Mg2+ free. Glycerol free is ideal for automation and free drying applications.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Combination Buffer, 2,500U
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 Combination Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer, Tween free, 5,000U
AS ONE 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. AS ONE Taq DNA Polymerase has both a 5 prime to 3 prime DNA polymerase and a 5 prime to 3 prime' exonuclease activity. The enzyme lacks a 3 prime to 5 prime exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A overhang, which makes the enzyme ideal for TA cloning. Included with Taq is Tween free 10x Ammonium Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Ammonium Buffer, 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 free 10x Ammonium Buffer.
As One International Inc Hot Start Taq Polymerase 5U/ul, 10x Ammonium Buffer, Magnesium free, 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 magnesium free 10x Ammonium Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul, 10x Ammonium Buffer and 10x Combination Buffer, 1,000U
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. Taq Polymerase includes 10x Ammonium Buffer and 10x Combination Buffer
AMID BIOSCIENCES Amid Biosciences, Lambda Protein Phosphatase, Recombinant, Protein Dephosphorylation, 20000 Units
Lambda Protein Phosphatase is supplied in a 20000 Units format for enzymatic dephosphorylation of proteins and related biomolecules. Lambda PP is the 221 amino-acid product of the ORF221 open reading frame on bacteriophage lambda. The enzyme is inhibited by vanadate ions and can be heat inactivated at 65 C for 1 hour in the presence of 50 mM Na2EDTA.The enzyme is useful for removing phosphate groups from serine, threonine, tyrosine, or histidine phosphorylated proteins in biochemical workflows. Applications include protein dephosphorylation, phosphoprotein cleanup, kinase assay workflows, production of unphosphorylated protein samples. Technical specifications are included below.- Quantity - 20,000 Units- Purity - greater than 90%- Activity - 600,000 Units/mg. One unit will hydrolyze 1 nmol of p-nitrophenyl phosphate, pNPP, in 1 minute at 30 C and pH 7.5 in a total reaction volume of 50 uL- Storage - -80 CThis product is for research use only.
As One International Inc Red-Taq DNA Polymerase 2x Master Mix, 1.5 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 5 U/ul glycerol free, 2,500U
Taq DNA Polymerase 5 U/ul glycerol free. Glycerol free is ideal for automation and free drying applications
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer and 10x Combination Buffer both Magnesium free, 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 magnesium free 10x Ammonium Buffer and 10x Combination Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul glycerol free, 10x Ammonium Buffer and 10x Combination buffer both Magnesium and detergent free , 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 Tween/Triton/magnesium free 10x Ammonium Buffer and 10x Combination Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul, 10x Ammonium Buffer and 10x Standard Buffer, 1,000U
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 are 10x Ammonium Buffer and 10x Standard Buffer.