My Life is suppose to be easier.
Hi, I was told by others that I was very lucky that I could use TLC to run activity assays on a protein whose structure we recently solved with NMR. TLC was suppose to be easier then our traditional approach of performing the assay on a large gel.
I'm having lots of problems getting readable results. Is there anyone who can suggest a good protocol or can provide any subtle hints to the technique.
The substrate is 5' labeled tRNAHis.
|All times are GMT. The time now is 02:52 PM.|
Powered by vBulletin® Version 3.8.4
Copyright ©2000 - 2015, Jelsoft Enterprises Ltd.
Copyright 2005 - 2012 Molecular Station | All Rights Reserved