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  1. Mix contents gently and incubate at 42oC for 2 minutes. 0 units) of Super cript IIaa , mix by 50 minutes at 42oC. Inactivate the reaction by heating at 70o C for 15 minutes. The cDNA can …

  2. cDNA Synthesis Protocol in Five Steps - Thermo Fisher Scientific

    Five steps to achieve effective cDNA synthesis through optimized sample preparation, genomic DNA removal, and reverse transcriptase enzyme selection.

  3. cDNA Synthesis - NEB

    Learn about the process of cDNA Synthesis, the generation of complementary DNA (cDNA) from an RNA template by reverse transcription.

  4. cDNA Synthesis and Quantitative PCR (qPCR) for Gene ... - Springer

    Apr 24, 2025 · This protocol outlines the steps for cDNA synthesis and subsequent quantitative PCR, from RNA extraction to data analysis. It also provides guidance on designing qPCR …

  5. cDNA Synthesis for RT-PCR Protocol Section of Cancer Genomics, Genetics Branch, NCI National Institutes of Health

  6. cDNA Synthesis using M-MLV Reverse Transcriptase (protocol adapted from ThermoScientific Reverse Transcriptase Cat. No. 28025) M-MLV RT (200 U/μL) (Thermo Scientific Cat. no. …

  7. A one-tube double-stranded cDNA synthesis system has been designed using M-MLV reverse transcriptase for first strand synthesis. Based on the Gubler and Hoffman procedure, the one …

  8. Pipette 5 l of diluted cDNA into all wells. Pipette 5 l of each primer pair mixture into triplicate wells. Note: if the experiment requires multiple plates, a control primer (housekeeping gene) is run in …

  9. In the first step, cDNA is synthesized using an RT primer that contains an adaptor of known sequence at the 5′ end. This primer, in conjunction with a template switching oligo (TSO), …

  10. cDNA Synthesis and Quantitative PCR (qPCR) for Gene Expression …

    This protocol outlines the steps for synthesizing complementary DNA (cDNA) from RNA samples, followed by quantitative PCR (qPCR) amplification to analyze gene expression.