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For DNA sequencing through high GC regions and rapid sequencing from nanogram amounts of DNA templates.
For replicating difficult templates in various applications.
DNA polymerase, thermotoga neapolitana was identified[1] as an enzyme able to withstand the protein-denaturing conditions (high temperature) required during PCR[2].
HOTaq DNA Polymerase is hot-start Taq DNA Polymerase, which is a modified form of Taq DNA Polymerase. HOTaq DNA Polymerase is provided in an inactive state and has minimum enzymatic activity at ambient temperatures.
For high-fidelity PCR and primer-extension reactions; PCR cloning and blunt-end amplification product generation.
Taq DNA Polymerase (exo+ and polymerase-) is a thermally stable, processive, 5'→3' DNA polymerase. The 94 kDa protein possesses an inherent 5'→3' nick-translation moiety and lacks a 3'→5' proofreading function. The DSC formulation contains a novel, nucleic-acid based hot-start additive designed to sequester the polymerase during reaction setup and during low-temperature cycling reaction phases.
Taq DNA Polymerase (full length exo-) is a thermally stable, processive, 5'→3' DNA polymerase. The 94 kDa protein possesses an inherent 5'→3' nick-translation moiety and lacks a 3'→5' proofreading function. The DSC formulation contains a novel, nucleic-acid based hot-start additive designed to sequester the polymerase during reaction setup and during low-temperature cycling reaction phases.
Taq DNA Polymerase (Klenow Fragment) is a thermally stable, processive, 5'→3' DNA polymerase. The 94 kDa protein possesses an inherent 5'→3' nick-translation moiety and lacks a 3'→5' proofreading function. The DSC formulation contains a novel, nucleic-acid based hot-start additive designed to sequester the polymerase during reaction setup and during low-temperature cycling reaction phases.
Taq DNA Polymerase (regular) is a thermally stable, processive, 5'→3' DNA polymerase. The 94 kDa protein possesses an inherent 5'→3' nick-translation moiety and lacks a 3'→5' proofreading function.
Taq DNA Polymerase (truncated and exo-) is a thermally stable, processive, 5'→3' DNA polymerase. The 94 kDa protein possesses an inherent 5'→3' nick-translation moiety and lacks a 3'→5' proofreading function. The DSC formulation contains a novel, nucleic-acid based hot-start additive designed to sequester the polymerase during reaction setup and during low-temperature cycling reaction phases.
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