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Last updated: 2017/2/19

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Product Name、Description and Alias
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10 x Taq Buffer

10 x Taq Buffer is a ready-to-use buffer to be used for Taq, Hot Taq, Red Taq and Long Taq enzymes in PCR reactions. Does not contain MgCl2.

  • • PCR

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10 x Taq Buffer with (NH4)2SO4

10 x Taq Buffer with (NH4)2SO4 is a ready-to-use buffer to be used for Taq, Hot Taq, Red Taq and Long Taq enzymes in PCR reactions. Does not contain MgCl2.

  • • PCR

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2 x HotTaq PCR Mix with MgCl2

HotTaq PCR mix is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant Taq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.

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2 x RedTaq PCR Mix with MgCl2

2 x RedTaq PCR Mix with MgCl2 is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant LongTaq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.

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2 x Taq PCR Mix with MgCl2

Taq PCR mix is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant Taq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.

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25 mM MgCl2

25 mM MgCl2 can be used for optimization of magnesium ion concentration in PCR reaction.

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HotTaq DNA Polymerase

HotTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. Prior the first PCR step the HotTaq DNA polymerase should be activated by 15 minute incubation at 95-97°C.

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LongTaq DNA Polymerase

LongTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure.

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PCR Water

Manufactured and tested for use as a component in PCR reactions. Validated as well for use with highly sensitive PCR reaction including those with eubacterial primer sets. Stored in convenient 2 mL tubes to avoid unnecessary melting and freezing of the whole water supply.

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Pfu DNA Polymerase

In addition to 5'-3' DNA polymerase activity, it also possesses 3'-5' exonuclease (proofreading) activity. Pfu DNA Polymerase exhibits the lowest error rate of any thermostable DNA polymerase studied, is even up to ten fold more accurate than normal Taq DNA polymerase. Consequently, Pfu DNA Polymerase is useful for polymerization reactions requiring high-fidelity synthesis.

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RedTaq DNA Polymerase

RedTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure. Added inert dye will not have any interference to the reaction. Visual confirmation that the enzyme has been added and proper component mixing of the reaction has occurred. Samples can be loaded directly onto an agarose gel for electrophoresis with no loading dye addition.

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Taq DNA Polymerase

Taq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure.

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