On 7 Sep 1997 13:09:48 GMT, remeans at fas.harvard.edu (Robert Means)
wrote:
>> Can anybody give me a pointer to a method for looking at very
>small shifts, say 2Kd in mobility in >100Kd proteins? I have tried running
>long, low percentage gels, but this doesn't seem to be enough. Thanks,
>Bob Means
>REMeans at fas.harvard.edu>
i assume you are trying SDS-PAGE. how about IEF gels? the 2 kDa change
may change the pI enough to allow resolution. or if you have purified
protein, try SDS-PAGE of some kind of a partial digest of the protein
and look for difference in banding patterns. then there always is
mass-spec.
bip
Bipin K. Dalmia, Ph.D.
Protein Expression and Purification
Pioneer Hi-Bred International, Inc.
Johnston, Iowa 50131
dalmiabk at phibred.com
