i am getting contamination in RNA that results in improper Actin Band. I use Trizol method for RNA extraction. Suggestion and tips needed or any protocol that you used and get no contamination.
The first thing that you may practice is that to isolate the RNA in sterile conditions. secondly, use DNase I to remove DNA contamination. I can give you a good protocol if you can tell me from which source you want to isolate RNA.