Those are the EasyXtal 15 well tools with the EasyXtal DG-Crystal Supports. 
Look at this link to find them: 
http://www.qiagen.com/products/protein/crystallization/default.aspx



I agree that they keep the drops from spreading out, but I have experienced 
trouble harvesting smaller crystals from these xtal tools.



Good luck!

Bryan



From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of Rob 
Gillespie
Sent: Wednesday, November 07, 2012 9:19 AM
To: [email protected]
Subject: Re: [ccp4bb] Problems in crystallization



Qiagen used to sell hanging-drop trays with screw-cap tops, and the tops had 
six rings on them (3 large, 3 small).  The rings had a lip on them that kept 
the drop from spreading beyond the edge.  I found these quite useful when 
setting up drops that had detergent in them.



I unfortunately don't know what they are called, as I have several at my bench 
but not the packaging they arrived in.



On Wed, Nov 7, 2012 at 9:04 AM, Eva Bligt-Lindén <[email protected]> wrote:

Thank you for your replies. To my knowledge the protein is not a 
surface-tension-reducing-protein and there is no detergent in the sample. I 
have tried different plates and still the same result. I will try a different 
crystallization technique such as batch under oil or counter-diffusion if I do 
not solve this problem. But now I am curious to know what is causing the 
disturbed surface tension and if someone else has experienced and dealt with 
something similar.

Kind regards,
Eva


Quoting anna anna <[email protected]>:

Why don't you try batch under oil?

2012/11/7 Eva Bligt-Lindén <[email protected]>

        Dear ccp4 users,

        I have a problem in the crystallization of my target protein. Whenever I
        set up a vapour diffusion experiment, either hanging or sitting drops, 
the
        drops spread out. The surface tension is completely lost in 80-90% of 
the
        droplets. Have any one experienced something similar? What could be the
        reason for this strange behaviour? I have tried three different 
commercial
        screens with 96 condition each and there is no difference between the
        screens. There is no difference between manual or robotic setups either.
        The protein buffer is 40 mM Tris, 2 mM MgCl2 buffer, pH 7.4. The buffer
        controls are all ok.

        Kind regards,
        Eva

        ______________________________**______



        Eva Bligt-Lindén (M.Sc.)
        PhD student
        Structural Bioinformatics Laboratory

        Department of Biosciences,
        Åbo Akademi University
        BioCity, Tykistökatu 6A
        FI-20520 Turku
        Finland






____________________________________

Eva Bligt-Lindén (M.Sc.)
PhD student
Structural Bioinformatics Laboratory

Department of Biosciences,
Åbo Akademi University
BioCity, Tykistökatu 6A
FI-20520 Turku
Finland




--------------------------------------------------------------------------
Confidentiality Notice: This message is private and may contain confidential 
and proprietary information. If you have received this message in error, please 
notify us and remove it from your system and note that you must not copy, 
distribute or take any action in reliance on it. Any unauthorized use or 
disclosure of the contents of this message is not permitted and may be unlawful.
 

Reply via email to