Enzymes
Our Enzymes have been tested and proven to be very high quality with robust and reliable results. They have been helping scientists worldwide achieve better results, saving their time and research funding.
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Sale!Intact Genomics FastAmp® Plant Direct RPA kit offers a fast, robust method for amplifying DNA fragments from plant tissues at a single and constant temperature (37°C) using RPA technology. The key highlights of FastAmp® Plant Direct RPA Solution include its simplicity, speed, and reliability. By eliminating the need for DNA extraction, researchers can streamline their workflows, with tissue lysis and genomic DNA ready for RPA in just 3 minutes.
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Sale!FastAmp® qRPA SYBR Kit is a powerful tool to screen primer conditions for the lowest possible Non-template control (NTC) background. Applications and Benefits:
- Primer validation and screening.
- Highly selective and sensitive isothermal amplification technique.
- Alternative to PCR. No thermocycler needed.
- Speed and sensitivity.
- No DNA pretreatment required.
- Flexible endpoint detection compatibility (e.g. lateral flow, real-time fluorescence).
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Sale!New improved IG® Recombinase Polymerase Amplification (RPA) Kit v2 provides a mixture of the necessary enzymes to simplify and quicken the setup for your RPA reaction.
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i7® High-Fidelity DNA Polymerase 2x master mix is a ready to use premix which contains high-fidelity DNA Polymerase, dNTPs, MgCl2, PCR enhancers and stabilizers with optimized proprietary reaction buffer. i7® High-Fidelity DNA Polymerase 2x master mix has the high-fidelity, sensitivity and processivity with an error rate ~2.8x102 fold lower than Taq DNA polymerase, and significantly lower than the error rates of other proofreading enzymes.
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Sale!Bsu DNA Polymerase I, Large Fragment is suitable for various purposes including RPA (Recombinase Polymerase Amplification)
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Sale!FastAmp® DNA, RNA Solution for Isothermal Amplification streamlines DNA and RNA collection and storage processes (including sample collection, transport, maintenance, viral/cell lysis, and viral RNA stabilization).