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PR1MA™ Taq

  • Ideal for routine PCR applications as well as genotyping, colony PCR, and fast PCR
  • Improved template affinity and solubility for higher enzyme activity and greater yields
  • Proprietary buffer optimized for a variety of assay conditions
  • Conveniently supplied as a 2X Master Mix or in a 2-tube format of polymerase and separate 5X buffer

 

PR1MA™ Taq provides superior results for routine applications. Modified to improve DNA-binding, this polymerase offers higher solubility and greater template affinity, resulting in consistently superior performance. PR1MA™ Taq Polymerase exhibits a 5' to 3' nuclease activity, but no 3' to 5' (proofreading) activity and works well with a wide range of DNA templates including GC-rich sequences.

 

The polymerase is supplied with a 5X buffer containing MgCl2 and a proprietary mix of enhancers (dNTP's not included). For convenience, PR1MA Taq is also available in a ready-to-use 2X Master Mix - just add primers and template DNA. Our "Red Dye" Master Mix incorporates a red-loading dye that allows amplified samples to be loaded directly on an agarose gel.  The red color aids in visualization during pipetting, and higher density of the buffer ensures that the samples will drop into the gel wells.

 

 

 
PR1MA™ High Fidelity Polymerase

  • 50X higher fidelity than Taq DNA polymerase
  • Works with crude DNA sample
  • Ideal for cloning, mutagenesis and microarrays
  • Produces blunt end products, to clone directly into blunt end vectors
  • Optimized buffer system with unique PCR enhancers

 

For applications requiring highly accurate amplification, choose PR1MA™ High Fidelity DNA polymerase. Modified for better solubility and higher activity across a broad range of ionic conditions, this polymerase will amplify a wide range of targets, including those that are GC or AT rich as well as crude samples.

 

A 3'-5' proofreading exonuclease activity and an error rate of 4.55×10-7 makes PR1MA™ High Fidelity DNA Polymerase the perfect partner for cloning applications. The supplied 5X buffer with dNTPs is optimized for compatibility with a variety of targets.

 

Specifications

Item DescriptionVolume
PR1000-HF-SPR1MA™ High Fidelity DNA Polymerase20 Units (Sample)
PR1000-HF-200PR1MA™ High Fidelity DNA Polymerase200 Units (2 U/p1)
PR1000-HF-500PR1MA™ High Fidelity DNA Polymerase500 Units (2 U/p1)
PR1000-HF-1000PR1MA™ High Fidelity DNA Polymerase1,000 Units (2 U/p1)


 

  


PR1MA Bst DNA Polymerase

 

PR1MA Bst polymerase (patent pending) is a recombinant, truncated, thermostable Bacillus stearothermophilus DNA polymerase with high reverse transcriptase and strand-displacement activities, ideal for isothermal amplification of RNA and DNA targets. PR1MA Bst polymerase has increased sensitivity and speed relative to other Bst polymerases and can incorporate dUTP. 

 

Use PR1MA Bst polymerase to develop LAMP assays with high sensitivity and specificity.

  • Lacks 5’ to 3’ exonuclease activity
  • Only Bst polymerase in the market with robust RT and DNA polymerase activity
  • Thermostable, working temperature range 64 - 72°C
  • Tolerant to inhibitors
  • Storage temperature: - 20°C

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCls
  • 1 mM DTT
  • 0.1  mM EDTA
  • 0.05% Tween – 20
  • 0.05% NP - 40 substitute
  • pH = 7.5

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.  
 


PR1MA Taq DNA Polymerase

 

Saves time and cost by enabling direct PCR amplification of unpurified templates. PR1MA Taq DNA polymerase is a recombinant, truncated (lacks 5’ to 3’ exonuclease activity), highly thermostable DNA polymerase from the thermophilic bacterium Thermus aquaticus. The enzyme is thermostable up to 98°C for polymerase chain reaction assays. It is supplied with 4 M betaine to improve amplification of GC-rich DNA and 30% sucrose to improve amplification from inhibitor-rich substrates such as blood.

  • Lacks exonuclease activity
  • Thermotolerant up to 98°C
  • Resistant to inhibitors, e.g., whole blood
  • Ideal for GC-rich templates
  • Storage temperature: -20°C
  • 10X PR1MA buffer, 4 M Betaine, and 30% Sucrose included

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • 0.5% Tween-20
  • 0.5% NP-40 substitute
  • pH = 7.5 

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
 


PR1MA Taq DNA Polymerase 1X Master Mix

 

PR1MA DNA polymerase 1X Master Mix saves time and cost by enabling direct PCR amplification of unpurified templates. It contains a recombinant, truncated (lacks 5’ to 3’ exonuclease activity), highly thermostable DNA polymerase from the thermophilic bacterium Thermus aquaticus. The enzyme is thermostable up to 98°C for polymerase chain reaction assays and is provided as a complete reaction master mix consisting of reaction buffer, dNTPs, MgCl2, and loading dye and only requires the addition of primers and DNA template. Once PCR is complete, the reaction products can be loaded directly into an agarose gel for analysis.

  • Lacks exonuclease activity
  • Thermotolerant up to 98°C
  • Inhibitor Resistant
  • Ideal for colony PCR, genotyping, and GC-rich templates
  • Storage temperature: -20°C 

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

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