8889005

Invitrogen™ Platinum™ SuperFi II DNA Polymerase

Invitrogen Platinum SuperFi II DNA Polymerase is a proofreading DNA polymerase that combines superior fidelity with an innovative buffer, enabling universal primer annealing for the highest success in PCR.

Manufacturer: Fischer Scientific

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GC-Rich PCR Performance

High

Reaction Speed

Fast

For Use With (Application)

Hot-start PCR, High-fidelity PCR

Hot Start

Built-In Hot Start

Reaction Format

Standalone

Polymerase

Platinum SuperFi II DNA Polymerase

Shipping Condition

Dry Ice

Fidelity (vs. Taq)

>300X

Overhang

Blunt

Size (Final Product)

20 kb or less

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Description

  • Invitrogen Platinum SuperFi II DNA Polymerase is a proofreading DNA polymerase that combines superior fidelity with an innovative buffer, enabling universal primer annealing for the highest success in PCR
  • Due to the unique composition of the SuperFi II PCR buffer, the annealing temperature is 60°C for most primer pairs designed following the general design rules
  • Features of Platinum SuperFi II DNA Polymerase include: Exceptional >300X Taq fidelity Universal primer annealing at 60°C Superior specificity, sensitivity, and yields Robust amplification of difficult-to-amplify targets Platinum SuperFi II DNA Polymerase is an engineered enzyme with high processivity and increased resistance to PCR inhibitors
  • It also enables fast-cycling protocols and amplification of long targets (up to 20 kb)
  • Platinum hot-start technology is based on proprietary antibodies that inhibit enzyme activity until the initial PCR denaturation step, preventing non-specific amplification and primer degradation
  • This technology also enables reaction setup at room temperature and provides increased sensitivity and yield
  • Isostabilizing molecules in the buffer increase primer-template duplex stability during the annealing step and contribute to enhanced specificity without the need to optimize the annealing temperature for each primer pair
  • With Platinum SuperFi II DNA Polymerase, different PCR assays can be cycled together using the same protocol with a universal primer annealing temperature and an extension step selected for the longest fragment to be amplified
  • Applications High-fidelity PCR Cloning and sub-cloning Site-directed mutagenesis Amplification of GC-rich templates Template generation for sequencing High-throughput PCR Amplification of samples with suboptimal purity Long PCR

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GC-Rich PCR Performance:
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Reaction Format:
Standalone

Polymerase:
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Polymerase:
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Shipping Condition:
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Fidelity (vs. Taq):
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