Reverse transcriptase reagent kit qScript XLT 1-Step ToughMix
RT-qPCRfor nucleic acidshemoglobin

Reverse transcriptase reagent kit - qScript XLT 1-Step ToughMix - QuantaBio - RT-qPCR / for nucleic acids / hemoglobin
Reverse transcriptase reagent kit - qScript XLT 1-Step ToughMix - QuantaBio - RT-qPCR / for nucleic acids / hemoglobin
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Characteristics

Type
reverse transcriptase
Applications
for nucleic acids, RT-qPCR
Tested parameter
hemoglobin
Storage temperature

Max.: -15 °C
(5 °F)

Min.: -25 °C
(-13 °F)

Description

Tough-tested 1-step real time PCR Features & Benefits Tough Tested – Overcomes common inhibitors including polysaccharides, heme/hemoglobin, humic acid, melanin Flexible – Use fast or standard qPCR cycling conditions Broad dynamic range- Reliable data from your precious samples every time Multiplexing enabled – Supports highly sensitive detection for up to four targets qScript XLT 1-Step RT-qPCR ToughMix is intended for molecular biology applications. This product is not intended for the diagnosis, prevention or treatment of a disease. Description 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. First-strand cDNA synthesis and subsequent PCR amplification are carried out seamlessly in the same reaction mixture with optimized 1-step thermal cycling parameters. This kit is ideal for highly sensitive quantification of RNA viruses or low abundance RNA targets as well as high throughput gene-expression studies. The system has been optimized to deliver maximum RT-PCR efficiency, sensitivity, and specificity in minimal reaction volumes and accelerated thermal cycling rates. The only necessary user-supplied materials for RT-qPCR is RNA sample and probe assay. It is compatible with all types of molecular probe assays including dual-labeling strategies. Elevating cDNA synthesis reaction temperature to 50-55°C during one-step RT-qPCR improves primer annealing and disruption of RNA secondary structure that can interfere with cDNA synthesis.

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