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Finnzymes’ High Performance PCR offers high fidelity PCR performance with increased yields in just a fraction of the time when compared to conventional PCR. We deconstructed the PCR process and created a tripartite solution that improves nearly every measurable aspect of PCR. It combines highly processive proofreading Phusion™ DNA Polymerases, high-speed Piko™ Thermal Cyclers, and ultra-thin walled UTW™ tubes and plates. Each component alone is best in class. Together they offer synergies that propel PCR to unbeatable performance. Download the High Performance PCR Brochure |
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Speed - Significantly faster than any other combinationTo save valuable research time, each component of the High Performance PCR solution is designed to expedite PCR protocols. Phusion DNA Polymerases are highly processive, due to a DNA-binding domain fused to the polymerase. |
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Yield - Higher efficiency amplification results in more productHigh-speed PCR is often fickle – variable yields depend upon the purity of template and the need for tedious reaction optimization. This is not true for our integrated solution. Phusion technology offers several distinct advantages. First, |
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Fidelity - Superior accuracy over Taq and Pfu based productsAt the core of our unique polymerases is a cleverly engineered proofreading enzyme with enhanced DNA-binding activity and processivity. The Phusion technology improves the fidelity of the polymerase , such that Phusion High-Fidelity DNA Polymerases have the lowest error rates of any polymerases available. The error rate of Phusion DNA Polymerases is as low as 4.4 x 10-7 , which is more than 50-fold better than that of Taq DNA polymerase. High Performance PCR may be used in routine applications or with protocols requiring the highest accuracy.
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Specificity - Reduced levels of primer-dimers and false-primed productsPrimer-dimers and false-primed products are not only a nuisance, but may mask the correct target amplicon. Our integrated solution combats this by speeding up and heating up the reaction. The Piko Thermal Cycler uses fast ramping and short annealing times to reduce the effects of spurious amplification by minimizing false priming. These unwanted products are diminished by Phusion DNA Polymerases´ ability to dramatically raise annealing temperatures as compared with conventional PCR. To further improve specificity in PCR, Phusion DNA Polymerases are also available as hot start enzymes utilizing "zero-time reactivation." |
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