Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : EMQZ1407
| Cat. No. | EMQZ1407 |
| Description | Taq DNA Polymerase (regular) is a thermostable enzyme with a highly processive 5''->3'' polymerase activity and 5''->3'' exonuclease activity. The enzyme is purified from E.coli and consists of a single polypeptide with a molecular weight of 94 kDa. Taq DNA polymerase synthesizes DNA from single-stranded templates in the presence of dNTPs and a primer. |
| Source | A recombinant E. coli strain that carries the cloned Taq DNA Polymerase gene from Thermus aquaticus YT-1. |
| Concentration | 5,000 U/ml |
| Applications |
• PCR (ordinary and high-throughput) • Primer Extension • Microarray Analysis • Denaturing high performance liquid chromatography (DHPLC) |
| Size | 400 U; 2,000 U |
| Unit Definition | One unit is defined as the amount of enzyme that will incorporate 10 nmol of dNTP into acid insoluble material in 30 minutes at 72°C. |
| Reaction Conditions | 100 ul reaction system containing: 1×standard Taq Reaction Buffer [10 mM Tris-HCl (pH 8.3 at 25 °C),50 mM KCl,1.5 mM MgCl2]; DNA template,primers,200 µM dNTPs and 2-5 U DNA polymerase. |
| Storage | Store at -20°C |
A: When used, dilute it to 1×, and its amplification speed is 1kb/min.
A: It is recommended to run 30-35 cycles for template amplification, while up to 40 cycles for bacterial PCR.
A: If there is stock available, it can be delivered within 3-5 days. If there is no stock available, it should not take more than a week for delivery.
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When used for bacterial PCR, the amplification effect is good and cheap.
The PCR product of Taq DNA polymerase will have an extra A at the 3' end, which can be ligated to a complementary T on the plasmid.
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