After DNasing Ronit’s RNA earlier today, I needed to check for any residual gDNA.
Identified some old, old C.gigas 18s primers that should amplify gDNA:
- gigas18s_fw (SRID 157)
- gigas18s_rv (SRID 156)
Used some old C.gigas gDNA (BB15 from 20090519) as a positive control.
Samples were run on Roberts Lab CFX Connect (BioRad). All samples were run in duplicate. See qPCR Report (Results section) for plate layout, cycling params, etc.
qPCR master mix calcs (Google Sheet):