Just wanted to pick your brains about a lil' prob our lab has been having with Trizol.
I have isolated RNA using Trizol for years and years and have never had a problem. A couple of months ago, our nanodrop curves started looking awful after isolation. We suddenly get high absorbance at about 220nm. As I understand it, this is phenol or guanidine contamination...If I precipitate the RNA, then the curves are lovely. But what worries me is that this pesky 220nm peak persists even with a new batch of Trizol, chloroform etc etc.
Does anyone have any ideas why we are suddenly having trouble with Trizol???
Have a great weekend
Clare















