Kit PCR (P1041)

67 €

Taq 2X Mix Kit is a premixed, ready-to-use solution containing Taq DNA Polymerase, dNTPs and Reaction Buffer at optimal concentrations for efficient amplification of DNA templates by PCR. In this kit, Taq DNA Polymerase is stored separately from PCR reaction Mix. To prepare the final PCR, please mix the polymerase and the reaction Buffer in appropriate proportion, and then add the primers and template DNA needed. Taq Mix Kit contributes to highly reproducible PCR by reducing the risk of pipetting errors, miscalculation and contamination. It also contributes to higher sensitivity by adding enhancer. Using the kit in your PCR reaction results in 3’-dA overhangs PCR products.

Taq DNA Polymerase, derived from the Thermus aquaticus, has been shown to exhibit superior thermostability. Its molecular weights is 94 kDa. And it can amplify template of up to 5 kb. This enzyme possesses a 5’ to 3’ polymerase activity but lacks a 3’ to 5’ exonuclease activity. Using Taq DNA Polymerase in your PCR reaction results in a 3’-dA overhangs PCR products.



2x PCR reaction mix: 1mL x 5

Taq DNA polimerase (2.5U/mL): 160μL


·The system contains sufficient reagents suitable for 200 amplification reactions of 50 μl each.
·The Mix already contains 4 mM MgCl2, and we provide another 25 mM MgCl2, this can be used to optimize the concentration of Mg2+ in your PCR system.


Convenient: only primers and template are needed
Efficiency: simplifying the operation and saving your time
Reproducible: reduce the risk of pipetting errors, miscalculation and contamination
Flexible: the amount of polymerase is flexible and controllable.


High throughput, high reproducible routine PCR
Generate PCR product for TA cloning

Unit Definition

One unit is defined as the amount of the enzyme required to catalyze the incorporation of 10 nM of dNTPs into an acid-insoluble form in 30 minutes at 70°C using hering sperm DNA as substrate.


2X PCR buffer, 0.4mM dNTPs, 3.2 mM MgCl2, 0.02% bromophenol blue.

Storage Buffer

20mM TrisCl ( pH8.0), 100mM KCl, 3.2mM MgCl2 1mM DTT,0.1% Triton X-100 ,0.1% Tween20, 0.2mg/ml BSA, 50% (v/v) glycerol.

Basic PCR Protocol

1. Add the following components to a sterile 50 μl microcentrifuge tube sitting on ice:


2. Mix contents of tube and overlay with 50 μl of mineral or silicone oil.
3. Cap tubes and centrifuge briefly to collect the contents to the bottom.
4. Incubate tubes in a thermal cycler at 94°C for 3 minutes to completely denature the template.
5. Perform 25-35 cycles of PCR amplification as follows:


6. Incubate for an additional 10 min at 72°C and maintain the reaction at 4°C. The samples can be stored at -20°C until use.

Notes on cycling conditions
  • Initial denaturation can be performed over an interval of 1-5 min at 95℃ depending on the GC content of template.
  • Optimal annealing temperature is 5℃ lower than the melting temperature of primer-temperature DNA duplex. If nonspecific PCR products are obtained optimization of annealing temperature can be performed by increasing temperature stepwise by 1-2℃.
  • The number of PCR cycles depends on the amount of template DNA in the reaction mix and on the expected yield of the PCR product. 25-35 cycles are usually sufficient for the majority PCR reaction. Low amounts of starting template may require 40 cycles.
  • The time of the final extension step can be extended for amplicons that will be cloned into T/A vectors.

7. Analyze the amplification products by agarose gel electrophoresis and visualize by ethidium bromide staining. Use appropriate molecular weight standards.

Store all components at –20°C



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