cDNA synthesis Bacteria

The formation of DNA from an RNA template using reverse transcription leads to the formation of double-stranded complementary DNA or cDNA. The challenges with this process include 1. Maintaining the integrity of RNA, 2. Hairpin loops or other secondary structures formed by single-stranded RNA can also affect cDNA synthesis, and 3. DNA-RNA hybrids, which may result when the first strand of cDNA is formed. For the first challenge, using workflows that involve proper isolation and storage of RNA, and maintaining a nuclease-free environment helps obtain RNA with ideal 260/230 ratios. Using a reverse transcriptase that can tolerate high temperatures (50-55oC), overcomes obstacles imposed by secondary RNA structures. Finally, RNase H has the ability to hydrolyze RNA before the formation of a second cDNA strand. It is important to ensure that RNase H activity is optimal because higher RNase H activity leads to premature degradation of the RNA template. Many reverse transcriptases offer built-in RNase H activity.

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5 years ago

5 years ago by Stefan Fuhrmann Germany

Will presence of EDTA effect cDNA synthesis

I intend to use iScript cDNA Synthesis Kit in order to synthesize cDNA for qPCR. I have confirmed that my RNA is pure however, according to my extraction protocol I have suspended the RNA in TE buffer containing 1mM EDTA. Will the presence of EDTA have an effect on cDNA synthesis?

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Found 12 matching solutions for this experiment

Upstream tips
The 5x TransAmp™ Buffer provides highly optimized components for efficient reverse transcription, and includes a unique blend
of anchored oligo dT and random hexamer primers to ensure unbiased 3’ and 5’ coverage for enhanced data accuracy.

For highly-structured RNA,increase the incubation temperature from 42C to 48 °C for 15 min
Protocol tips
Mix RNA sample and primer d(T)23VN and denature RNA for 5 minutes at 70°C.

Add M-MuLV Reaction Mix and
M-MuLV Enzyme Mix and incubate reaction at 42°C for one hour.

Inactivate the enzyme at 80°C for 5 minutes
Protocol tips
After DNAse treatment add Oligo dT Primer,dNTP Mixture,Template RNA and RNase-free dH O and heat at 65°C for 5 min.

Add reaction mix to the above mix and incubate at 30°C 10 min*
and 42 to 50°C for 30 to 60 min
Protocol tips
Incubate for 2 min at 42°C. Then place immediately on ice.

Add reverse-transcription master mix and incubate for 15 min at 42°C.

Incubate for 3 min at 95°C to inactivate Quantiscript Reverse Transcriptase
Protocol tips
Prepare transfection master mix and mix throughly by pippetting.

Add 15ul master mix to 5ul of RNA for each RT reaction.

Adjust the volume of water if the input of RNA is not to 5 ul input (1ug-1pg)
Upstream tips
Reliable for Sensitive transcription of both high-copy and low-copy messages.

Reverse Transcriptase is active
across a range of 37–55°C, with greatest activity at 37–42°C
Protocol tips
Add 0.5 ul (10 U) of Reverse Transcriptase to the reaction mix and incubate for Incubate 30 min at 55°C.

Inactivate Transcriptor Reverse Transcriptase by heating to 85°C for 5min
First-Strand cDNA Synthesis Kit

GE Healthcare Life Sciences

Protocol tips
Heat the RNA solution to 65ºC for 10 minutes, then chill on ice.

Add first-strand cDNA reaction mix and incubate at 37°C for 1 hour
Power cDNA Synthesis Kit

iNtRON Biotechnology

Protocol tips
Incubate at 40℃ in heat block (or water bath) for 60 min, and heat to 94℃ for 5 min terminating the reaction
Protocol tips
Add reaction mix and incubate at 37°C for 30 min.

Add 1 µL 50 mM EDTA and incubate at 65°C for
10 min.
Protocol tips
When required, cDNA product can be diluted with 10 mM Tris-HCl (pH 8.0), 0.1 mM EDTA
iScript cDNA Synthesis Kit

Bio-Rad Laboratories

Protocol tips
Follow product thermal cycling conditions
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