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DNA polymerases are enzymes that synthesize DNA molecules from nucleoside triphosphates. Products include various types of DNA polymerases, kits, buffers, and other reagents for DNA amplification.
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 (1)Applications• Strand displacement DNA synthesis (2)• Random primer labeling• Second strand cDNA synthesis• dA-tailing
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A high-fidelity thermostable DNA polymerase isolated from Pyrococcus furiosus, produced in E. coli through recombinant expression. This enzyme is engineered for PCR applications requiring enhanced accuracy in DNA synthesis.
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Thermolabile USER (Uracil-Specific Excision Reagent) II Enzyme generates a single nucleotide gap at the location of a uracil residue. It can be 100% inactivated at temperatures >65C.
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Unique blend of highly-efficient MyTaq HS DNA Polymerase and a proprietary proofreading enzyme that combine to give increased target affinity for use with challenging templates and inhibitor-rich samples.
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Thermolabile USER (Uracil-Specific Excision Reagent) II Enzyme generates a single nucleotide gap at the location of a uracil residue. It can be 100% inactivated at temperatures >65C.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Therminator DNA Polymerase is a 9N DNA Polymerase variant with an enhanced ability to incorporate modified substrates such as dideoxynucleotides, ribonucleotides and acyclonucleotides.
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DNA Polymerase I, Large (Klenow) Fragment is a proteolytic product of E. coli DNA Polymerase I which retains polymerization and 3' to 5' exonuclease activity, but has lost 5' to 3' exonuclease activity. Klenow retains the polymerization fidelity of the holoenzyme without degrading 5' termini.
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fastStart(TM) Taq DNA Polymerase is a versatile enzyme that can be used in a wide variety of applications and on multiple instrument platforms. This modified thermostable recombinant Taq DNA polymerase is inactive at temperatures below 75 C but is activated by a 2 to 4 minute heat activation step at 95 C. Since it is inactive at low temperatures fastStart(TM) Taq DNA Polymerase cannot elongate non-specific primer-template hybrids that may form at those temperatures. fastStart(TM) Taq DNA Polymerase is an ideal tool for hot start PCR because the enzyme remains inactive during PCR set-up and prior to the initial denaturation step.
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