I am trying to extract RNA, from grape berries of a red variety, for qPCR (to study gene expression). I have tried nucleozol and a CTAB protocol (with b-mercaptoethanol+boric acid + cleaning with chloroform, but without success (Actually after cleaning with chloroform and transferring the supernatant, I added isopropanol to the supernatant and got 2 liquid fractions instead of a pellet (after centrifuge)). Do you have an idea why that happens? Can someone please suggest a protocol?