I do phenol-chloroform RNA extraction. But after running the samples on gel electrophoresis, I see more DNA. What should I do to reduce genomic DNA during RNA extraction?
The most common and effective method for removing trace to moderate amounts of DNA contamination from RNA samples is digestion with DNase I, a nonspecific endonuclease that selectively cleaves DNA (both single and double stranded) by hydrolyzing phosphodiester bonds. The DNase must be inactivated or removed from the reaction before subsequent PCR applications; otherwise, it may digest newly amplified DNA.