AMV First Strand cDNA Synthesis Kit
- This product was discontinued on 01/01/2017
The AMV First Strand cDNA Synthesis Kit combines AMV Enzyme Mix and AMV Reaction Mix. The AMV Enzyme Mix is an optimized blend of AMV Reverse Transcriptase and a Murine RNase Inhibitor. AMV Reverse Transcriptase provides first strand cDNA synthesis reactions with a broader optimal reaction temperature from 37°C to 50°C. The Murine RNase Inhibitor is less sensitive to oxidation than the human RNase inhibitor, leading to better protection of RNA templates. The AMV Reaction Mix is an optimized buffer including dNTP. In the presence of the 1X AMV Reaction Mix, the AMV Enzyme Mix produces long cDNA products with high yield (up to 10 kb).
The first strand cDNA products generated by AMV Enzyme Mix are suitable for downstream gene cloning, quantitative analysis by standard PCR or real-time PCR.
General Information for Successful cDNA Synthesis:
Intact RNA of high purity is essential for sensitive RT-PCR detection. RNA should have a minimum A260/A280 ratio of 1.7 or higher.
Either total RNA or mRNA can be used in the reverse transcription reaction. Total RNA is generally sufficient for most RT-PCR analyses. However, if desired mRNA can be easily obtained using a PolyA Spin mRNA Isolation Kit (NEB #S1560) or Magnetic mRNA Isolation Kit (NEB #S1550).
The amount of RNA required for detection depends on the abundance of the transcript of interest. In general 1 ng to 1 μg total RNA or 0.1-100 ng mRNA are recommended.
First Strand cDNA Synthesis Reaction
Denaturation of RNA and primer at 70°C for 5 minutes can remove secondary structures that may impede long cDNA synthesis. However, this step can be omitted in some cases (unpublished results).
We recommend incubation at 42°C for one hour for maximum yield and length. However, many targets can be detected after a much shorter incubation time. For example, 5 minutes incubation is enough for a 2 kb cDNA synthesis.
Higher reaction temperature up to 60°C can be used for difficult targets of high secondary structures.
Choice of Primers for Reverse Transcription
Oligo d(T) priming is preferred for most applications because it ensures that all cDNA copies terminate at the 3´ end of the mRNA and produces the longest contiguous cDNA. An anchored oligo-d(T) primer [d(T)23VN] forces the primer to anneal to the start of the polyA tail, thereby preventing priming at internal sites in the polyA tail (1). However, two other priming choices are possible if desired.
The Random Primer Mix is an optimized mix of hexamer and d(T)23VN primers. It provides random priming sites covering the entire RNA templates including both mRNAs and non-polyadenylated RNAs (such as ribosomal RNAs). The Random Primer Mix yields shorter cDNAs on average and can be used for the detection of multiple short RT-PCR products. Random Primer Mix offers good performance in a wide range of RNA templates.
When a gene-specific primer is used in a cDNA synthesis reaction, the cDNA product can be used only for amplification of that transcript. This priming method gives good results when the amount of RNA is limiting (below 10 ng) and only one particular cDNA is desired.
Recommended primer concentration:
PRIMER -- Final conc.
OLIGO d(T)23VN -- 5 μM
RANDOM PRIMER MIX -- 6 μM
SPECIFIC PRIMER -- 0.1–1 μM
The following reagents are supplied with this product:
Store at (°C) Concentration Nuclease-free Water -20 AMV Enzyme Mix 10 X AMV Reaction Mix 2 X Oligo d(T)23 VN -20 50 μM Random Primer Mix -20 60 μM
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