I guess this has been asked before, but as an old hand at protein
purification but new to inclusion bodies, what do people find the best
way to renature from 6M urea?
Cheers,
R
--
Richard P. Grant MA DPhil
Structural Studies Group, MRC-LMB
http://www2.mrc-lmb.cam.ac.uk/personal/rpg/index.html
Please reply to rpg 'at' mrc-lmb.cam.ac.uk