Taq DNA Polymerase Combo - Enzyme Combo LA
€0.00
In stock
SKU
VN250EC
Catalog Number: VN250EC
Size: KlenTaq LA 25 μl, OmniTaq LA 25 μl, OmniTaq 3 LA, Omni Klentaq 2 LA 25 μl
Other Size(s):
Datasheet
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Size: KlenTaq LA 25 μl, OmniTaq LA 25 μl, OmniTaq 3 LA, Omni Klentaq 2 LA 25 μl
Other Size(s):
Datasheet
Request Information
Taq & KlenTaq Pols and Master Mixes (6)
Taq DNA Polymerase is a thermostable enzyme that synthesizes DNA from single-stranded templates in the presence of dNTPs and a primer. The enzyme consists of a single polypeptide with a molecular weight of 94 kDa. It has a 5´→3 DNA polymerase activity and a 5´→3´ exonuclease activity. Recombinant enzyme is purified from the cloned Thermus aquaticus DNA polymerase gene expressed in E. coli.
KlenTaq® is a Klenow-fragment analog of Taq DNA polymerase. It is a 5’-exonuclease deficient Taq polymerase (an N-terminal deletion of Taq) with improved fidelity, robust and thermostability.
KlenTaq-S is a 5’-exonuclease deficient Taq polymerase (an N-terminal deletion of Taq) with improved fidelity and thermostability, plus an extra mutation rendering the enzyme PAP function (Pyrophosphorolysis-activated polymerization). The enzyme is capable of detecting rare mutations, large heterozygous deletions, gene duplications, etc. in the presence of a large excess of wild type allele and inorganic pyrophosphate). In theory PAP can detect a single base mutation in 3x1011copies of wild type allele.
Taq and Klentaq LA® (Long Accurate) versions of the enzymes are mixtures of Taq / KlenTaq and a proof reading enzyme. They can be used to amplify a long gene target with high fidelity.
Enzyme Combo or Enzyme Combo LA contains several most popular Taq DNA polymerase mutant enzymes to allow scientists test to see which one works best for their application.
Taq DNA Polymerase is a thermostable enzyme that synthesizes DNA from single-stranded templates in the presence of dNTPs and a primer. The enzyme consists of a single polypeptide with a molecular weight of 94 kDa. It has a 5´→3 DNA polymerase activity and a 5´→3´ exonuclease activity. Recombinant enzyme is purified from the cloned Thermus aquaticus DNA polymerase gene expressed in E. coli.
KlenTaq® is a Klenow-fragment analog of Taq DNA polymerase. It is a 5’-exonuclease deficient Taq polymerase (an N-terminal deletion of Taq) with improved fidelity, robust and thermostability.
KlenTaq-S is a 5’-exonuclease deficient Taq polymerase (an N-terminal deletion of Taq) with improved fidelity and thermostability, plus an extra mutation rendering the enzyme PAP function (Pyrophosphorolysis-activated polymerization). The enzyme is capable of detecting rare mutations, large heterozygous deletions, gene duplications, etc. in the presence of a large excess of wild type allele and inorganic pyrophosphate). In theory PAP can detect a single base mutation in 3x1011copies of wild type allele.
Taq and Klentaq LA® (Long Accurate) versions of the enzymes are mixtures of Taq / KlenTaq and a proof reading enzyme. They can be used to amplify a long gene target with high fidelity.
Enzyme Combo or Enzyme Combo LA contains several most popular Taq DNA polymerase mutant enzymes to allow scientists test to see which one works best for their application.
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