Hi All
I have a ligand that is dissolved in 100% DMSO. The ligand crashes out even
when diluted to 20% final DMSO concentration in the protein buffer. I have
heard of people using detergents such as n octyl Beta D glucoside to keep the
ligand solubilized at lower DMSO concentrations. Can
Dear all
I am interested in crystallizing a 5 residue peptide. I have no prior
experience in this field although I have crystallized larger proteins (5--60
kDa). Do people use regular screens used in macromolecular crystallization
such as Hamptons, wizards etc? Any suggestions are greatly
