In article <f05210601bc5800da3305@[193.146.54.140]>, ahernan at cica.es wrote:
> Thanks to all,
>> I think I'll try Mike Sullivan's suggestion but with a stacking on
> top (maybe 3% ).
> As for the presence of SDS, the protein and the RNA are (hopefully!)
> crosslinked, so, if there are no problems with size, the complex
> should enter the gel and stay put.
> Anyone heard about a Tris-Acetate system, anyway?
> Cheers
>> Agustin
Search for Jovin buffers (span the entire pH range).
You can find more information in the book: Gel electrophoresis a practical
approach.
Roland
> ---
