2X Pro Taq Premix (with dye) II

Product Code: AG11113

- +

¥210

Product Description

Pro Taq DNA Polymerase is synthesized on our superior performance Accurate Taq High fidelity enzyme has been added to the enzyme to provide 3′→5′ Exonuclease activity (Proof reading activity), which is ideal for amplification of DNA fragments over 10 kb and has good fidelity. This product is a 2-fold concentration PCR reaction premix, containing Pro Taq DNA Polymerase, dNTPs and optimized Buffer system, PCR reaction, just add the template, primers and water to the premixed solution can be amplified. At the same time, the product is also added with the coloring reagent required for electrophoresis testing, the solution of the product is purple-red in color, and it can be used for agarose gel electrophoresis directly after the PCR reaction is completed. The premixed solution is easy to use, minimizes human error, reduces the risk of multi-step contamination, and provides results in a short period of time. The PCR product has an A base at the 3’ end and can be cloned directly into T vectors.

Product Advantages

① The product is a 2X premix, only need to add template, primer and water to the premix for amplification, easy to operate, can minimize human error, reduce the possible contamination caused by multi-step operation, and the results can be obtained in a relatively short period of time.
② 2X Pro Taq Master Mix (dye plus) II has good amplification performance, amplifying ~30 kb of DNA fragments using λDNA as a template and ~12 kb of DNA fragments using Human genomic DNA as a template.
③ The product contains violet dye, after PCR can be directly carried out agarose gel electrophoresis, without adding electrophoresis sample buffer, electrophoresis has a light violet-red indicator band.

Product Composition
individual parts making up a compound norm
2X Pro Taq Master Mix (dye plus) II 500 μl x 6 pc
RNase free water 1 ml x 3 pc
Preservation and transportation
Storage temperature: -20℃
Transportation temperature: dry ice transportation or -20℃ ice bag transportation
Example 1

Human gDNA and λDNA were used as templates, and different lengths of DNA fragments were amplified using this kit, and good amplification results were obtained.

The electrophoresis results are shown below:

Example 2

The human gDNA was used as a template to amplify DNA fragments with high AT and high GC content, and both fragments were well amplified by this kit.

The electrophoresis results are shown below:

Example 3

Using Human gDNA as template, the kit amplifies 2 kb DNA fragments with different template amounts (500 ng, 200 ng, 100 ng, 10 ng, 1 ng, 100 pg), and amplifies the target fragments at template amounts as low as 1 ng.

The electrophoresis results are shown below:

table of examples of experiments
Template Type Amplification speed Fragment size (kb) Sequence GC content Withdrawal method template volume Can it be amplified
Human gDNA 30 sec / kb 0.5 kb 46.2% reagent method 100 ng
Human gDNA 1 min / kb 0.5 kb 35.7% reagent method 100 ng
Human gDNA 1 min/ kb 0.5 kb 75.4% reagent method 100 ng
Human gDNA 30 sec / kb 1 kb 36.1% reagent method 100 ng
Human gDNA 30 sec / kb 2 kb 38.1% reagent method 100 ng
Human gDNA 1 min / kb 2.1 kb 26.9% reagent method 100 ng
Human gDNA 1 min / kb 3 kb 38.7% reagent method 100 ng
Human gDNA 1 min / kb 3.4 kb 39.2% reagent method 100 ng
Human gDNA 1 min / kb 4 kb 36.0% reagent method 100 ng
Human gDNA 1 min / kb 4 kb 38.2% reagent method 100 ng
Human gDNA 1 min / kb 10 kb 37.7% reagent method 100 ng
Human gDNA 1 min / kb 12 kb 37.2% reagent method 100 ng
Mouse gDNA 1 min / kb 1 kb 52.2% Magnetic bead method 100 ng
Mouse gDNA 1 min / kb 3.4 kb 53.4% Magnetic bead method 100 ng
Chicken gDNA 1 min / kb 0.5 kb 41.0% Magnetic bead method 74 ng
Chicken gDNA 1 min / kb 1.2 kb 36.6% Magnetic bead method 75 ng
Chicken gDNA 1 min / kb 1.7 kb 68.6% Magnetic bead method 76 ng
Chicken gDNA 1 min / kb 2.4 kb 49.4% Magnetic bead method 77 ng
Pig gDNA 1 min / kb 0.6 kb 47.6% Magnetic bead method 30 ng
Pig gDNA 1 min / kb 2 kb 57.9% Magnetic bead method 31 ng
Tomato gDNA 1 min / kb 0.5 kb 28.2% Magnetic bead/column method 120 ng
Tomato gDNA 1 min / kb 1.6 kb 32.2% Magnetic bead/column method 120 ng
Tomato gDNA 1 min / kb 1.9 kb 36.0% Magnetic bead/column method 120 ng
Tomato gDNA 1 min / kb 3 kb 37.4% Magnetic bead/column method 120 ng
Tomato gDNA 1 min / kb 4.4 kb 38.1% Magnetic bead/column method 120 ng
λDNA 30 sec / kb 25 kb 51.6% 2 ng
λDNA 30 sec / kb 30 kb 51.6% 2 ng
Escherichia coli colony 1 min / kb 1 kb 53.8% / single colony
Escherichia coli colony 1 min / kb 2 kb 51.1% / single colony
Escherichia coli colony 1 min / kb 3.5 kb 52.2% / single colony
Escherichia coli colony 1 min / kb 5 kb 53.2% / single colony
Escherichia coli colony 1 min / kb 6.7 kb 51.8% / single colony
Escherichia coli colony 1 min / kb 11 kb 50.7% / single colony

Note: √ indicates able to amplify, / indicates not extracted. -indicates direct purchase.