RNA gels - staining and denaturing

[Darren D. Browning]

I have had no problem at all visualising RNA in formamide gels simply by adding a drop (about 
50ul of etbr to the 1x MOPS running buffer.  Before running, the gel doesn't have any etbr in 
it.  This method allows you to re-use the 1x MOPS running buffer several times without 
needing to reach for fresh etbr every time you pour a gel.

-- 
Darren Browning                    __________
Rm.116 Department of Immunology   [  ______  ]
The Scripps Research Institute,   [ [  ___   ]
10666 North Torrey Pines Rd.      [ [ [      ]
La Jolla California               [ [ [      ]
92032                             [ [        ]
                                  [__________]
Tel. (619) 554-1142               
Fax. (610) 554-8483
email: dbrownin at scripps.edu