I intend to separate ribosomal and non-ribosomal fractions of cytosol using 20% sucrose cushion. I have already run the cell lysate on top of the 20% sucrose solution for 2 hrs at 1,39,000 g. I could not find any separate layer of ribosomal fraction or did not get any pellet. Should I use fractionator to separate the fractions? Please provide me a suitable procedure.
Thanks in advance.