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Hotstart Taq DNA Polymerase (5u/ul) HC1012B Featured Image
  • Hotstart Taq DNA Polymerase (5u/ul) HC1012B

Hotstart Taq DNA Polymerase (5u/ul)


Cat No:HC1012B

Package:250U/1000U/1000U/25000U

Taq DNA Polymerase is a hot start DNA polymerase with double blocking by double antibodies.

Product Description

Product detail

Product Tags

Taq DNA Polymerase is a hot start DNA polymerase with double blocking by double antibodies.This product not only blocks the 5′→3′ polymerase activity of Taq DNA polymerase,but also blocks the 5′→3′exonuclease activity. Heating for 30 seconds at the pre-denaturation temperature can completely inactivate the antibody and release DNA polymerase activity and exonuclease activity. The double blocking characteristic can not only effectively prevent the nonspecific amplification caused by mismatch or primer dimer, but also effectively inhibit the decline of fluorescence signal caused by probe degradation, so as to make the in vitro detection reagent more stable during transportation or use at room temperature.


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  • Components

    Component

    HC1012B

    (250U)

    HC1012B

    (1000U)

    HC1012B

    (10000U)

    HC1012B

    (25000U)

    Taq DNA Polymerase(5 U/μL)

    50 μL

    200 μL

    2 mL

    5 mL

     

    Storage Condition

    The product is shipped with dry ice and can be stored at -25°C~-15°C for 2 years.

     

    Specifications

    Polymerase

    Taq DNA Polymerase

    Purity

    ≥ 95% (SDS-PAGE)

    Hot Start

    Built-in Hot Start

    Reaction Speed

    Standard

    Exonuclease Activity

     5′→3′

     

    Instructions

    Reaction Setup

    Components

    Volume (μL)

    Final Concentration

    2× Buffer a

    25

    Primer/Probe mix b 

    ×

    0.1 μmol/L-0.5 μmol/L

    Hotstart Taq Polymerase (5U/μL)

    1.2

    0.12 U/μL

    DNA Template c

    ×

    0.1-100 ng

    ddH2O

    Up to 50

    -

    Notes:

    1) According to the specific experimental application, it is needed to prepare the corresponding reaction buffer.

    2) The amount of DNA and the concentration of probes or primers are recommended concentrations. The optimal concentration can be adjusted according to the specific experimental conditions.

     

    Thermal cycling protocol

    Step

    Temperature (°C)

    Time

    Cycles

    Pre-denaturation

    95 ℃

    5mins

    1

    Denaturation

    95 ℃

    15 sec

    45

    Annealing / Extension

    60 ℃ a

    30 sec b

    Notes:

    1) The reaction temperature is adjusted according to the Tm value of the designed primers.

    2) Different qPCR instruments need different fluorescence signal acquisition time, please set according to the shortest time limit.

     

    Notes

    Please wear the necessary PPE, such lab coat and gloves, to ensure your health and safety!

     

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