INTRO
After isolating RNA earlier today (Notebook) for the project-gigas-carryover/lifestage_carryover
(GitHub repo), I proceeded with reverse transcription for those samples with sufficient yields of RNA.
MATERIALS & METHODS
Reverse transcription was run using 100ng of each sample, using M-MLV reverse transcriptase (Promega) and oligo dT primers (Promega), according to the manufacturer’s protocol (PDF). Oligo dT primers and M-MLV reverse transcriptase amounts were adjusted to maintain the proper ratio, relative to the amount of input RNA.
Calculations:
- 20240319-cgig-carryover-spat-seed-cDNA-calcs (Google Sheet)
RESULTS
cDNA was stored in the -20oC freezer in FTR 213.
Box layout: