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2×GS Taq PCR Mix For PAGE (ST112)

2×GS Taq PCR Mix For PAGE (ST112)

1) Suitable for conventional PCR amplification and PCR amplification of shorter DNA fragments, dedicated to polyacrylamide electrophoresis detection.

2) High yield.

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Product Description

1) Suitable for conventional PCR amplification and PCR amplification of shorter DNA fragments, dedicated to polyacrylamide electrophoresis detection.

2) High yield.




Highlights


    Simple operation: 2×Mix, only need to add primers, template and ddH2O for PCR amplification.




Introduction

   

    This product contains high-purity GS Taq DNA polymerase, dNTPs and an optimized buffer system with a concentration of 2×. PCR amplification can be performed only by adding primers, templates and ddH2O. It is suitable for conventional PCR and PCR amplification of shorter DNA fragments. Increase, dedicated to polyacrylamide electrophoresis detection.

    The PCR product amplified by this product has a protruding "A" base at the 3' end, which can be directly used for TA cloning after purification.




Composition


Contents

Amount

2×GS Taq PCR Mix For PAGE

5×1.0 mL




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Q1Why is there no product or a small amount of product in the final result?

A1

    1)Template degradation or poor template purity. Use electrophoresis to check template quality and use high-quality templates.

    2)The template concentration is too low. Appropriately increase the template usage.

    3)The primers are not suitable. Optimize primer design.

    4)The annealing temperature is not suitable. Set the annealing temperature gradient and explore the appropriate annealing temperature.

    5)The number of cycles is too small. Appropriately increase 5~10 cycles.

    6)Insufficient extension time. For complex templates, the extension speed can be appropriately increased to 20~30 s/kb.

 

Q2Why do non-specific bands or diffuse bands appear in amplification?

A2

    1)Poor primer specificity. Optimize primers to avoid nonspecific bands and amplification of primer dimers.

    2)The primer concentration is too high. Decrease primer concentration.

    3)Template excess or poor purity. Reduce the amount of templates and use high-quality templates.

    4)The annealing temperature is too low. Appropriately increase the annealing temperature or use the Touchdown PCR program.

    5)Too many cycles. Reduce the number of cycles to 25~30 cycles.



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