Along those lines suggested by David I would say these crystals are way too big.
Try freezing some when they are smaller. It would also be worth trying to 
freeze in meshes to support the fragile plate instead of conventional loops.
J?rgen

......................
J?rgen Bosch
Johns Hopkins University
Bloomberg School of Public Health
Department of Biochemistry & Molecular Biology
Johns Hopkins Malaria Research Institute
615 North Wolfe Street<x-apple-data-detectors://4>, W8708
Baltimore, MD 21205<x-apple-data-detectors://5/0>
Office: +1-410-614-4742<tel:%2B1-410-614-4742>
Lab:      +1-410-614-4894<tel:%2B1-410-614-4894>
Fax:      +1-410-955-2926<tel:%2B1-410-955-2926>
http://lupo.jhsph.edu<http://lupo.jhsph.edu/>

On Apr 24, 2015, at 03:52, Hargreaves, David 
<[email protected]<mailto:[email protected]>> 
wrote:

The crystals don't look that bad in my opinion. Maybe the cryo step is sub 
optimal? Try using large loops (reduces surface tension forces during 
transfer). Butane 2,3 diol is a good cryo to try. Maybe shoot them at room temp 
(in situ) to get an idea of how they diffract before you manipulate them.
Good luck!

From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of Prerana G.
Sent: 24 April 2015 04:01
To: [email protected]<mailto:[email protected]>
Subject: [ccp4bb] Thin plate crystals

Dear all,
I am working on a protein (40kDa) which forms very thin plate shaped crystals 
which diffracts at very low resolution. Protein concentration that i have used 
for crystallisation is approx. 8mg/ml. I have attached the picture of the 
protein crystal.

How can I improve upon the shape of the crystal?
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