RNA gels - staining and denaturing

Darren D. Browning dbrownin at scripps.edu
Sat Jul 22 15:03:08 EST 1995


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               [ [ [      ]
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Tel. (619) 554-1142               
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email: dbrownin at scripps.edu





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