Transfected Stable Cell Lines
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Cat. No. : EMDT0316
| Cat. No. | EMDT0316 |
| Description | Phoenix Hot Start Taq DNA Polymerase is a recombinant, thermostabile Taq DNA polymerase complexed with a thermolabile, neutralizing antibody that blocks the 5′→3′ polymerase activity prior to the initial DNA denaturation step of PCR. Such antibody-mediated Hot-Start capability enhances the overall specificity, sensitivity and yield of the PCR by reducing nonspecific amplification and primer-dimer formation prior to PCR cycling, and allows the convenience of reaction set up at room temperature. When the temperature of the PCR reaction mix reaches ≥94 °C during the initial DNA denaturing step of PCR cycling, activity of the Taq DNA polymerase is fully restored. Phoenix Hot Start Taq DNA Polymerase, like standard Taq DNA polymerase, also has 5′→3′ exonuclease activity, but lacks any detectable 3′→5′ exonuclease activity. |
| Source | A recombinant E. coli strain carrying the Taq DNA polymerase gene from the thermophilic organism Thermus Aquaticus YT-1 complexed with a monoclonal antibody derived from murine cell culture. |
| Concentration | 5000 U/ml |
| Size | 500 Units |
| 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 75 °C. |
| Storage | 20 mM Tris-HCl100 mM NaCl0.1 mM EDTAStabilizer50% GlycerolpH 7.5 at 25 °C |
A: This enzyme has 5′→3′ exonuclease activity but lacks 3′→5′ exonuclease activity.
A: The enzyme complex contains corresponding antibodies, which mediate the hot-start capability by reducing nonspecific amplification and primer dimer formation before PCR cycling, thereby improving the overall specificity, sensitivity, and yield of PCR.
A: This enzyme is not active at room temperature to avoid primer dimer formation and nonspecific extension. Its activity can be restored by heating at 95°C for 4 minutes.
A: Yes, the 3'-end of the PCR product will have an additional adenosine (dA), resulting in a 3'-dA overhang in the target fragment.
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When using this enzyme for amplifying target fragments, there are very few primer dimers formed, resulting in high product specificity.
The reaction system can be prepared at room temperature without affecting the enzyme activity.
The Hot Start Taq DNA Polymerase is well-packaged and transported, and there are no quality issues with the product.
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