Reverse transcriptase reagent kit qScript 1-Step ToughMix
for molecular biologyRT-qPCRvirus

Reverse transcriptase reagent kit - qScript 1-Step  ToughMix - QuantaBio - for molecular biology / RT-qPCR / virus
Reverse transcriptase reagent kit - qScript 1-Step  ToughMix - QuantaBio - for molecular biology / RT-qPCR / virus
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Characteristics

Type
reverse transcriptase
Applications
for molecular biology, RT-qPCR
Micro-organism
virus, SARS-COV-2
Storage temperature

Max.: -15 °C
(5 °F)

Min.: -25 °C
(-13 °F)

Description

Superior sensitivity for viral RNA detection Features & Benefits Superior Sensitivity – higher yields optimized for lower viral RNA inputs Tough Tested – tolerant to a wide range of PCR inhibitors Multiplexing – Supports highly sensitive detection for up to four targets Broad Dynamic Range – Reliable data from your precious samples every time qScript 1-Step Virus ToughMix is intended for molecular biology applications. This product is not intended for the diagnosis, prevention or treatment of a disease. Description qScript 1-Step Virus ToughMix is a 2x, ready-to-use, master mix for rapid detection of RNA viruses such as Flu-A, Flu-B, and SARS-CoV-2, using one-step, or single-tube reverse transcription quantitative PCR (RT-qPCR). It has been optimized for maximum sensitivity to enable reliable quantification of very low input quantities of RNA using dual-labeled hydrolysis probe detection chemistries such as TaqMan® probes in single or multiplexed assay formats. qScript 1-Step Virus ToughMix contains all required components for RT-qPCR except RNA template and primer/probe assays. qScript 1-Step Virus ToughMix is powered by an engineered reverse transcriptase with reduced RNase H activity and improved activity and stability at higher temperatures, that includes a RT Hot-Start technology to suppresses non-specific primer extension by the RT before cDNA synthesis. The use of higher temperatures (50 to 55°C) for the first-strand step of one-step RT-qPCR provides higher specificity for primer annealing and disruption of RNA secondary structure that can interfere with cDNA synthesis.

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