Von Jagow and Schagger wrote a manual in 1995, A Practical Guide to Membrane
Purification, Academic Press, in which they suggest shrinking high percentage gels in
50% MeOH, 2% glycerol for 30-60 min and then drying at elevated temp. under vacuum.
In <5orive$6j0 at falcon.le.ac.uk>, "Dr E. Buxbaum" <EB15 at le.ac.uk> writes:
>skim at PLAZA.SNU.AC.KR wrote:
>>Dear everyone,
>>>>I am trying to detect the low molecular weight(8KD) protein using
>>Tris-Tricine SDS-PAGE. But when I dried the gel, the gel was easily
>>crashed.
>>I equilibrate my gels in 10% glycerol in aq. bidest. for 30 min before
>drying them. Keeps them nice and flexible.
>
