I extracted total RNA with the TRIZOL method and according to literature, I can digest ssRNA with RNase A in 2*SSC, but I don't know how to inactivate RNase and purify the mixture after RNase treatment. So could you help me?
You can cleanup your RNA by using RNeasy mini kit . Cleanup protocol is on page 54 of RNeasy® Mini Handbook http://www.qiagen.com/resources/download.aspx?id=14e7cf6e-521a-4cf7-8cbc-bf9f6fa33e24&lang=en