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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.
Thermus aquaticus DNA Polymerase (Taq DNA Polymerase) is a thermostable enzyme which can replicate DNA at 74oC and remain active even after incubation at 95oC. It has very strong 5’-3’ DNA polymerase activity with a fast extension rate. Although it lacks any 3’-5’ exonuclease activity (and therefore proofreading ability), Taq DNA polymerase remains one of the most widely used enzymes in molecular biology. Lamda Biotech’s bacterially derived Taq DNA Polymerase is unique for strong activity and low background in DNA amplification. This enzyme is purified from bacteria. Users should be cautious when dealing with bacteria DNA sequences.
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Bacteriophage T7 RNA Polymerase is a DNA-dependent RNA polymerase with strict specificity for the T7 phage promoter The enzyme is widely used for the synthesis of specific transcripts from DNA in the 5 3 direction as well as being a suitable model for studying the mechanisms of transcription The RNA produced by T7 RNA Polymerase is suitable for many downstream applications GenScript is offering T7 RNA Polymerase produced by expression in an E coli strain carrying a plasmid encoding the T7 RNA Polymerase
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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.
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Taq DNA Polymerase is a thermostable DNA Polymerase isolated from an E. coli strain that carries the Taq DNA polymerase gene. Taq DNA Polymerase is the most common polymerase used for PCR.Note: This product is supplied with 10X reaction buffer containing 15 mM magnesium chloride. dNTP (10 mM) mixture must be ordered separately (see related products).
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Radiant™ HiFi Polymerase Pro™ 2X RED Mastermix is a versatile and robust high fidelity DNA polymerase engineered for all PCR applications where greater sequence accuracy is required. Improved DNA binding and increased processivity result in shorter extension times, higher yields and the ability to amplify longer and more difficult targets. High temperature cycling – up to 100 °C denaturation to better separate GC-rich templates Increased PCR success rates with complex genomic templates (17.5 kb and over) High yields under standard and fast PCR conditions (10-30 s/kb) Efficient and specific amplification from challenging templates including GC and AT-rich sequences 100x higher fidelity than Taq DNA polymerase Generates blunt-end PCR products Available as a convenient 2x ready mix with the option of a red dye for direct gel loading
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