Dear Saurabh,

   Your crystals are gorgeous!

   Which cryoprotectant did you use?

   Best,

   Everton.

Sent from my iPhone

> On Mar 21, 2021, at 11:04 AM, Saurabh Upadhyay <saurabh807...@gmail.com> 
> wrote:
> 
> 
> Dear All,
> 
> I am trying to crystalize a protein, which occurs in monomeric (60kDa) and 
> tetrameric (240kDa) form. The protein during crystallization was in MES 
> buffer pH-6 and the method of crystallization was "Sitting drop" in "Proplex" 
> condition. Some of the conditions in which crystals were obtained are:
> 
> 1) 0.1M HEPES pH-7; 10% (w/v) PEG 4000
> 2) 0.1M Tris, pH-8; 8% (w/v) PEG 8000
> 3) 0.1M Tris, pH-8; 25% (v/v) PEG 400
> 
> For reference, I have attached the images of the crystals observed below.  
> 
> However, the diffraction pattern obtained and the resolution of crystals were 
> very poor. Even some mosaicity has been observed.  
> 
> Kindly suggest some methods or modifications, to improve the resolution and  
> diffraction pattern of the crystals obtained. 
> 
> Thanking You,
> Sincerely,
> Saurabh Upadhyay,
> Ph.D. Scholar
> c/o Dr. Ashok kumar Patel,
> Kusuma School of Biological Sciences,
> Indian Institute of Technology, Hauz Khas,
> New Delhi-110016, India
> 
> 
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> <Crystals by Sitting Drop.pptx>

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