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Foreasy Taq DNA Polymerase

◮ High specificity: The enzyme has a certain hot-start activity. ◮ Fast Amplification: 10 sec/kb. ◮ Highly adaptable template: can be used to efficiently amplify GC High value, various difficult-to-amplify DNA template.

◮ Strong fidelity: ordinary Taq Enzyme 6 times.

◮ Strong thermal stability: It can be placed at 37 °C for a week and maintains more than 90% activity.

Foreasy Taq DNA Polymerase is a new Taq enzyme expressed in Escherichia coli engineering bacteria by gene recombination technology. The enzyme itself has a certain hot-start activity and can be used for conventional PCR and qPCR; it has 5'→3' DNA polymerase activity and 5'→3' exonuclease activity, but no 3'→5' exonuclease activity.- High specificity: The enzyme has a certain hot-start activity. - Fast Amplification: 10 sec/kb . - Highly adaptable template: can be used to efficiently amplify GC High value, various difficult-to-amplify DNA template. - Strong fidelity: ordinary Taq Enzyme 6 times. - Strong thermal stability: It can be placed at 37 °C for a week and maintains more than 90% activityVarious PCR/qPCR systems and direct PCR systems PCR amplification of DNA fragments DNA labeling DNA sequencing PCR A-tailed

Component	IM-01011	IM-01012	IM-01013
Foreasy Taq DNA Polymerase(5 U/μL)	5000 U (1 mL)	50 KU (10 mL)	500 KU (100 mL)
2× Taq Reaction Buffer	25 mL ×5	250 mL ×5	500 mL ×25

-20 ± 5 °C for 2 years or at -80 °C for long-term storage.1U: The amount of enzyme required to incorporate 10 nmol of deoxynucleotides into acid-insoluble matter using activated salmon sperm DNA as template/primer for 30 minutes at 74°C.

Temperature	Time	Cycle
37°C	5mins	1
94°C	5mins	1
94°C	10 Secs	35
60°C	10 Secs
72°C	20 sec/kb
72°C	2mins	1

Foreasy Taq DNA Polymerase

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