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NaM203003_Lolina Hotstart Direct Taq DNA Polymerase(5 UμL)-Lolina

NaM203003_Lolina Hotstart Direct Taq DNA Polymerase(5 UμL)

    詳細(xì)說(shuō)明

    Lolina A/S

    Address: Sindalsvej 30 8240 Risskov Danmark 

                        Email: Info@lolina.dk

     Website: https://lolina.dk




    Product Specification

     

    Product

    Lolina?  Hotstart Direct Taq DNA Polymerase, 5 U/μL

    Catalog   No.

    NaM203003

    Storage   conditions

    Shipment with ice packs. Store at -20°C with a shelf life of  2 years.

    Hot Start

    Built-in   hot start

     

    Product description

     

    Lolina? Hotstart Direct Taq DNA Polymerase is a heat-activated DNA polymerase that is tolerant to blood and other inhibitors. This product utilizes antibody blocking and possesses excellent amplification sensitivity and specificity. The antibody is fully deactivated by heating at the denaturation temperature for 30 seconds, releasing the DNA polymerase activity. The use of this hot- start Taq enzyme effectively suppresses non-specific amplification caused by primer misannealing.

    Components

     


    Catalog No.

    Specification

    Volume

     

     

    Lolina?   Hotstart   Direct Taq  DNA  Polymerase,  5 U/μL

    NaM203003ES72

    250 U

    50 μL

    NaM203003ES76

    500 U

    100 μL

    NaM203003ES80

    1000 U

    200 μL

    NaM203003ES92

    10 KU

    1 mL× 2

    NaM203003ES93

    25 KU

    1 mL× 5

    NaM203003ES94

    50 KU

    10 mL

     

    Instructions

     

    1.Reaction System

     

    Components

    Volume(μL)

    Final   Concentration

    Buffera

    25

    1 x

    Primer/Probe mixb

    x

    0. 1 μM-0.5 μM

    Hotstart D-Taq (5 U/μL)c

    1.2

    0. 12 U/μL

    Template DNAd

    x

    0.1-100 ng

    ddH2O

    up to 50

    -

     


    [Note]:

    a)    According to the specific experimental application, it is necessary to prepare the corresponding reaction buffer.

    b)    The primer concentrations in the table are recommended concentrations. They can be adjusted according to the specific experimental conditions to achieve the optimal concentrations.

         c)    Adjust the amount of Taq enzyme according to the specific experimental application.

    d)    The DNA amount in the table are recommended concentrations. They can be adjusted according to the specific experimental conditions to achieve the optimal concentrations.

     



    2.Reaction   ro  ram


     

    Cyclestep

    Temp.

    Time

    Cycles

    Initial denaturation

    95°C

    5 min

    1

    Denaturation

    95°C

    15 s

    45

    Annealing/Extension

    60°Ca

    30 sb


    [Note]:

    a)    Amplification reaction: The amplification reaction temperature should be adjusted based on the Tm value of the designed primers.

    b)    Fluorescence signal collection: Different qPCR instruments require different fluorescence signal collection times. Please set the collection time according to the shortest time limit.

     

    Notes

     

    For your safety and health, wear lab coats and disposable gloves during operation.


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