![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
sharp peak in library - TruSeq Stranded Total RNA (rRNA-depleted E. coli) | Seqasaurus | Sample Prep / Library Generation | 1 | 11-05-2015 02:02 AM |
What does IGV track color alignments by strand when using non-stranded RNA-seq? | Villy | Bioinformatics | 3 | 03-20-2015 12:49 AM |
End repair of TruSeq RNA and TruSeq mRNA stranded | ykgenome | Sample Prep / Library Generation | 2 | 05-15-2014 12:01 AM |
Amplification of total RNA or cDNA quantities | fearnoweevil | Sample Prep / Library Generation | 0 | 02-14-2013 09:45 AM |
recover cDNA from total RNA for RNAseq? | mapplebe | Sample Prep / Library Generation | 3 | 08-21-2012 08:23 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Paris Join Date: Apr 2015
Posts: 1
|
![]()
Dear all,
I start my 1st automated experiment with TruSeq stranded total RNA. Unfortunately, my pipetting platform doesn't have a cooling block (I didn't choose this option when I bought it), my question is : - For the "Synthesize 1st strand cDNA" and "Adenylate 3' Ends" steps, basically, we need to incubate samples at 70°C then hold at 4°C. Can I process directly the next step without this 4°C, or use a cooling block passive (not controled temperature, so the temperature can be 4, 6, 10°C...)? Does anyone faced this problem? Help me please. Many thanks, |
![]() |
![]() |
![]() |
Thread Tools | |
|
|