Hi there!
I am crystallizing a 130 kDa protein which crystalizes under variety of
conditions and with different methods. Unfortenately the result is
always more or less the same, twinned crystals. Sometimes I get nice
looking ones, which look like single crystals. These often also turn out
to be twinned or have high mosaicity.
So, now I am asking you people out there for tips, what would you do in
my situation?
I'll preciate all tips!
Riikka Reitzer
