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Catalog Number | No. of Reactions | Color |
---|---|---|
14000012 | 50 reactions | Colorless |
14001012 | 50 Reactions | Green |
14001013 | 200 Reactions | Green |
14001014 | 1000 Reactions | Green |
14000014 | 1000 reactions | Colorless |
14000013 | 200 Reactions | Colorless |
Platinum II Hot-Start Green PCR Master Mix also includes two tracking dyes for direct loading of PCR products on gels.
Features
Applications
Platinum II Taq Hot-Start DNA Polymerase is an engineered Taq DNA polymerase that shows increased resistance to reaction inhibitors originating from sample material or DNA purification steps. The polymerase has a higher DNA synthesis rate and delivers PCR results more than two times faster than other Taq DNA polymerases. Proprietary Platinum Taq antibodies block polymerase activity at ambient temperatures and dissociate after the initial denaturation step at 94°C. This automatic hot start provides increased sensitivity, specificity, and yield, while allowing reaction assembly at room temperature.
Due to the unique composition of the Platinum II PCR buffer, the annealing temperature is 60°C for most primer pairs designed following the general design rules. Isostabilizing molecules in the buffer increase primer–template duplex stability during the annealing step and contribute to enhanced specificity without the need to optimize annealing temperature for each primer pair. With Platinum II Hot-Start PCR Master Mix (2X), different PCR assays can be cycled together using the same protocol with universal primer annealing temperature and the extension step selected for the longest fragment to be amplified.
Notes
Platinum II Taq Hot-Start DNA Polymerase products can be stored at 4 degrees C for up to 3 months. For longer storage, we recommend storing all components at -20 degrees C.
Electrophoretic separation on E-Gel agarose gels depends on the salt concentration in the analyzed sample. For optimal separation, we recommend diluting PCR reactions performed with colorless and green Platinum II PCR Master Mixes 2- to 20-fold, prior to running on E-Gel agarose gels. The dyes in the Platinum II Hot-Start Green PCR Master Mix do not interfere with fragment separation on E-Gel agarose gels.
No. The tracing dyes (a blue and a yellow dye) in Platinum II Green PCR Buffer do not interfere with PCR performance and do not change any enzyme features.
Yes, Platinum II Taq Hot-Start DNA Polymerase can be used in qPCR master mixes for target detection and quantification in a real-time PCR instrument using probes or SYBR Green dye.
Yes. Due to stable antibody-mediated hot-start technology, Platinum II Taq Hot-Start DNA Polymerase is highly stable. The premixed reactions for PCR can be incubated at room temperature for up to 24 hr before loading in the thermal cycler, without any loss of amplification specificity.
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