Dear ALL;
Recently I am purifying a cell surface receptor by refolding of its
inclusion bodies.
Actually I can purify some functional monomers of this protein. However,
the protein precipitates during the concentration. Interestingly, the
precipitates look like crystals but not
If they look like crystals, why don't you shoot them and see if they diffract ?
Some people have been lucky with this approach.
Jürgen
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Jürgen Bosch
Johns Hopkins Bloomberg School of Public Health
Department of Biochemistry Molecular Biology
Johns Hopkins Malaria Research Institute
615 North
