Also collect while rotating around the long axis, which you nearly are in this
shot assuming the Phi axis is horizontal.
That way the close separation is in x,y where you can see it rather than in Z
which puts the spots on top of each other requiring thin slicing and (low
mosaicity!) to
A 2-years funded postdoctoral research position is immediately available at
the newly established Structural Biology Group, at the Unit of Biophysics
(UB), University of the Basque Country (UPV/EHU), Spain. We are seeking a
highly motivated individual, interested to investigate the structural,
Thanks a lot for your suggestions.
Regards,
Prerana
On Fri, Apr 24, 2015 at 7:05 PM, Tanner, John J. tanne...@missouri.edu
wrote:
Following up on Dave's suggestion, you could try using crystal screens as
additives. This has worked well in my lab. The idea is to mix the
condition that you
A reference that describes what Jack is referring to is detailed here:
http://www.ncbi.nlm.nih.gov/pubmed/15858279
I have used this technique to improve every protein I have ever crystallised.
In the most extreme cases poorly diffracting hopeless crystals that were also
strongly anisotropic
