We offer reagents formulated with ultrapure Taq DNA Polymerase, which contains a stringent antibody hotstart to ensure specific and efficient primer extension. Our enzymes are rigorously purified to remove host E. coli genomic DNA and are ideally suited for applied testing applications. Available in a variety of optimized formulations designed to support specific PCR applications and starting materials.
PerfeCTa qPCR reagents combine a stringent, ultrapure antibody hotstart with performance engineered DNA polymerase in stabilized 1-tube formulations optimized for the specific performance needs of real-time quantitative PCR. Proprietary additives help eliminate persistent bubbles to enable efficient vortex mixing and fewer technical replicates. Adaptive buffer chemistry accommodates most assay designs and can be used with existing assay designs.
qPCR/qRT-PCR ToughMix reagents contain proprietary inhibitor-neutralizing additives that relieve several types of PCR inhibitors.
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qScript One-Step SYBR® Green RT-qPCR
The qScript One-Step SYBR® Green RT-qPCR Kit is a convenient and highly sensitive solution for quantitative RT-PCR of RNA templates (RT-qPCR) using SYBR Green I dye detection and gene-specific primers.
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qScript XLT 1-Step RT-qPCR ToughMix
qScript XLT One-Step RT-qPCR ToughMix is a ready-to-use, highly sensitive master mix for reverse transcription quantitative PCR (RT-qPCR) of RNA templates using hybridization probe detection chemistries such as TaqMan® 5′-hydrolysis probes.
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RapiDxFire Lyo-Flex 1-Step RT-qPCR 5X Master Mix
RapiDxFire™ Lyo-Flex 1-Step RT-qPCR 5X Master Mix is a convenient, single-tube master mix that provides sensitive and reproducible detection of bacterial and viral pathogens.
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RapiDxFire qPCR 5X Master Mix GF
High-performing, lyo-compatible master mix for sensitive pathogen detection.
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SuperROX Reference Dye
SuperROX is a passive reference dye used to normalise fluorescent signals in real-time PCR.
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UltraPlex 1-Step ToughMix
UltraPlex 1-Step ToughMix is a ready-to-use, 4X concentrated master mix 1-step reverse transcription and real-time quantitative PCR (RT-qPCR) of RNA templates using probe-based detection methods. First-strand cDNA synthesis and PCR amplification are carried out in the same tube without opening between steps.
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