Circular dichroism

Chris Larsen clarsen at
Tue Sep 13 08:57:47 EST 1994


You can measure helix content of your protein, and its binding
to the substrate, if there is any "pertubation spectra".
Check out Curtis Johnson on a medline search.

You can also measure for disappearance of secondary structure 
by denatuaration with heat, guanidine or urea.


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