thank you, it is a good idea! very simple to use!
Allison <"allison.haggartyREMOVE THIS"@mcgill.ca> wrote in message news:<3DB6AAEE.30F5059C at mcgill.ca>...
> FreD wrote:
>> > Hi all!
> >
> > i am a phd student (bordeaux, France;) and i have some problems with
> > an IP. My protein is about 30kDa, and the dimer is about 60kDa. So i
> > have some problems to see them on SDS-PAGE (thanks light and heavy IgG
> > chains!).
>> What if you run a gel without reducing agent. Then the intact antibody
> would run at 150K leaving your 30K and 60K bands on their own.
>> Allison
>>>
