Hey everyone!!
I'm using the High Capcity cDNA Reverse Transcription kit from applied biosystem. The kit comes with random primers, however I wanted to try oligo(dt) 15 primers. I was wondering if I would need to change my thermocycler conditions. everything I've seen online are kit specific so I'm not sure what I should do.
3 replies to this topic
#1
Posted 03 May 2012 - 10:30 AM
#2
Posted 03 May 2012 - 01:02 PM
The kit (superscript III) that I use says to incubate oligodT primed RNA at 50 deg C for 50 min, but for random hexamers to incubate at 25 deg C for 10 min, then 50 min at 50 deg C.
So it appears there is a minor difference in the conditions, but how this affects the product, I don't know.
So it appears there is a minor difference in the conditions, but how this affects the product, I don't know.
#3
Posted 24 August 2012 - 09:03 AM
We are comparing the High Capacity cDNA kit to our usual Superscript III First Strand Kit. I would like to know how things went with your try of oligos instead of the hexamers. We have always used oligos with the Superscript kit, and I'm hesitant to switch to hexamers in the High Capacity kit. Any comments?
Cheers,
-Joyce
Cheers,
-Joyce
Edited by joycef007, 24 August 2012 - 09:04 AM.
#4
Posted 26 August 2012 - 08:58 AM
I think Fermentas' cDNA premium kit is one of the best out there. we usually use gene specific primers (gsp) instead of random hexamers or oligo(dT). Our pcr works much better with gsp. we also heat our samples at 65C before addition of buffer and RT enzyme for 5 min. This is in the protocol. Again, pcr works better if we pre-incubate at 65C. After addition of RT we incubate at 50C for 30-45 min. I know superscript is very popular in the US, but I would still go for the premium kit from Fermentas. Thermo just bought them last year, so they must be sold under Thermo now.
Also tagged with one or more of these keywords: cDNA, Cloning
![]() |
Protocols and Techniques Forums →
Molecular Cloning →
Too many negative clones using Directional TOPO CloningStarted by Guest_zbiology_* , Yesterday, 07:02 PM |
|
|
|
![]() |
Protocols and Techniques Forums →
Genetics and Genomics →
Design construct for promoter activity assayStarted by Guest_DrLeo_* , Yesterday, 05:34 AM |
|
|
|
![]() |
Protocols and Techniques Forums →
Molecular Cloning →
"Easiest" sticky end combinationStarted by Guest_doxorubicin_* , 21 May 2013 |
|
|
|
![]() |
Protocols and Techniques Forums →
PCR, RT-PCR and Real-Time PCR →
Reproducible Non-Specific PCR ProductStarted by Guest_Epigeneticist_* , 20 May 2013 |
|
|
|
![]() |
Protocols and Techniques Forums →
Molecular Cloning →
classic cloning with restriction enzymes into empty pcDNA3.1DStarted by Guest_Euterpa12_* , 17 May 2013 |
|
|














