I am interested in people's experience in stabilizing nucleic acids, specifically RNA, in soft tissue samples (e.g., lymph nodes, bladder, prostate, breast, colon, and others) prior to running assays. Are there any tricks to working around the effects of formalin? Has anyone had any luck in getting docs to bypass formalin on select tissues that will be analyzed molecularly - requesting use of a different fixative or molecular prep solution? What success have people had in the race against time in RNA degradation?
Many thanks,
Bruce
DNA/RNA extraction from formalin fixed tissues
Started by anonymous, Apr 25 2001 09:00 PM
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