Reverse transcriptase reagent kit MB1730 series
for cDNA synthesisRT-qPCRliquid

Reverse transcriptase reagent kit - MB1730 series - NZYTech - for cDNA synthesis / RT-qPCR / liquid
Reverse transcriptase reagent kit - MB1730 series - NZYTech - for cDNA synthesis / RT-qPCR / liquid
Reverse transcriptase reagent kit - MB1730 series - NZYTech - for cDNA synthesis / RT-qPCR / liquid - image - 2
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Characteristics

Type
reverse transcriptase
Applications
RT-qPCR, for cDNA synthesis
Format
liquid
Method
enzymatic
Storage temperature

Max.: -15 °C
(5 °F)

Min.: -85 °C
(-121 °F)

Description

NZY M-MuLV First-Strand cDNA Synthesis Kit is a system that includes all the necessary components to synthesize first-strand cDNA, except the template RNA. Details NZY M-MuLV First-Strand cDNA Synthesis Kit, separate oligos, is a system that includes all the necessary components to synthesize first-strand cDNA, except the template RNA. Random hexamers and Oligo(dT)18 primers are provided in separate tubes to offer the convenience to choose the appropriate primer to initiate your reverse-transcription reaction. The resulting single-stranded cDNA is suitable for use in real-time quantitative Reverse Transcription PCR (RT-qPCR). NZY M-MuLV First-Strand cDNA Synthesis Kit, separate oligos, is formulated to provide high yields of full-length cDNA products and to increase sensitivity in RT-qPCR. Starting material can range from 10 pg up to 5 µg of total RNA. Besides random hexamers and Oligo(dT)18 primers, the kit includes NZYRT 2× Master Mix, no oligos, which contains dNTPs, MgCl2 and an optimized RT buffer; 10× Annealing Buffer and NZYM-MuLV RT Enzyme Mix. NZYM-MuLV RT Enzyme Mix includes both NZY M-MuLV Reverse Transcriptase (RNase H minus) and NZY Ribonuclease Inhibitor in order to protect RNA against degradation due to ribonuclease contamination. RNase H (from E. coli) is provided in a separate tube to specifically degrade the RNA template in cDNA-RNA hybrids after the first-strand cDNA synthesis. This procedure will improve the sensitivity of subsequent RT-qPCR reactions since PCR primers will bind more easily to the cDNA. Components – NZYM-MuLV RT Enzyme Mix – NZYRT 2x Master Mix, no oligos – 10× Annealing Buffer – Random hexamer mix (50 ng/µL)

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