Hello HengChiat,

 Could be that the brief exposure to air resulted in more nucleation sites.  
You could still 
measure data on your crystal of interest despite the presence of the tiny 
crystals, as they 
are not likely to diffract well enough to interfere with the primary 
diffraction pattern.   I 
would just go ahead and loop and flash-cool the crystal and let the X-rays tell 
you the 
answer.  If this is the case you need not worry about preventing the tiny 
crystals from 
growing.

Good luck!

-pam

==============Original message text===============
On Wed, 10 Jun 2009 12:20:55 pm CDT HanJie_HCT Tai wrote:


Hi,



My crystal was grown in 33%MPD/0.2M (NH4)2SO4/5% P400/0.1M tris in 500 ul well 
covered with 200ul paraffin oil. The droplet (0.9 ul protein + 0.9 ul reservoir 
+ 0.2 ul 30% 
DMSO) is hung over the cover slide.
 
Because of twining issue, when the small but single crystal showed up from the 
drop after 
overnight setting up, I transferred the cover slide to 30% MPD condition well 
IMMEDIATELY. 
(When crystal gets older, it tends to grow into multilayer form, stacking plate 
lies on the 
first crystal)
 
HOWEVER, after inspecting under microscope, I found that there were tremendous 
tiny 
crystals surround those single crystals :(
 
Any suggestion to improve this situation in order to avoid introducing any tiny 
crystal in the 
drop.
 
Additional Q: Should I include 3% DMSO in my cryosolution?
 
Regards,
HengChiat 


 


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-- 
----

Pamela J. Focia, Ph.D.
Research Assistant Professor

Structural Biology Facility Manager
Robert H. Lurie Comprehensive Cancer Center
in the Departments of:
Molecular Pharmacology and Biological Chemistry, Feinberg  School of Medicine,
and Biochemistry, Molecular Biology & Cell Biology, 
Northwestern University
303 E. Chicago Ave., S-215,  Chicago 60611
(312)503-0848   fax (312)503-5349
[email protected]



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