Hi everybody!
Just a small question, I want to reduce BrET use in my experiments and as we have only 1 microware used also for other people and things i prefer to use BrET on my TAE running buffer instead on gel.
In your experience wich is the smallest concentration of BrET I can use on my buffer in order to have a good DNA view?
Thanks a lot!
How Much BrET?
Started by sorcener, Jan 19 2010 10:40 AM
2 replies to this topic













