Taq DNA Polymerase is a highly thermally stable DNA polymerase derived from thermophilic bacteria Thermus aquaticus. This enzyme reaction requires the participation of Mg²+ and can catalyze the polymerization of deoxynucleotides dependent on DNA templates in the 5 'to 3' direction. The Taq DNA Polymerase developed by our company is a high-purity enzyme protein obtained by recombinant expression of the Thermus aquaticus DNA Polymerase gene in Escherichia coli and through multi-step chromatography separation and purification. It has the same properties as natural Taq DNA Polymerase.
Item No. : E02
Specification5 U/µL
It has 5 '-3' polymerase and 5 '-3' exonuclease activities; It has no 3 '-5' exonuclease activity and no calibration function.
Reagent composition
1.5 U/µL Taq DNA Polymerase
2.10×PCR Buffer Ⅱ (Mg²+free (Optional)
3.25mM MgCl₂ (optional)
*10×PCR Buffer Ⅱ (Mg²+free of dNTP and Mg²+When preparing the reaction system, please add dNTPs and MgCl₂ for use.
Product features
At 70 to 75℃, the elongation rate is 1 to 2 kb per minute.
2. The 3 'end of the PCR product is A, and the product can be directly cloned into a T vector.
3. Applicable to common PCR and RT-PCQualitative and quantitative detection of R.
4. It is applicable to fluorescence quantitative PCR detection, DNA sequencing, etc.
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