Hi Jim
I guess you are talking about coomassie stained SDS gels?? If that is
the case then you can extract the protein by excising the band and
placing it into an eppendorf tube with about 200uL of 100mM Na acetate,
0.1% SDS and 10mM DTT. Shake for 24hours at 37 deg C and most of the
protein will elute from the gel. The protein can be recovered in this
way for amino acid analysis, sequencing or whatever.