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- Protein crystallographyMain steps:- Protein purification- Crystallisation Special:- Programs for crystallography- X-ray detectors Basic tutorials:- Chemistry- Protein - Peptide - Amino Acids Xtal community:- CCP4BB |
CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999Subject: crystallisation From: sajid akthar b_sajid_ali {- at -} YAHOO {- dot -} CO {- dot -} IN Date: 2008-06-02 Dear All My protein size is ~30kD and crystallizes with 19%Peg3350, 0.2M Nacl, and 0.1M Na Cacodylate buffer. Please refer the attached crystal image with this. The crystal looks like good enough for home source. These crystals appears in 4-5 days at room temp. Sometimes I'm getting crystals like this, but very few in 24 well tray. Most of the time, I found the drop contains needles. If I reduce the precipitant little bit, I wont find any change in the drop even after long time. Changing pH (or temp)of the buffer does not help me any better. The crystal appears only around 5.5pH. The problem is mosaicity. This crystal diffracted in home source upto 3.2A and the mosaicity is 2.5degree. Almost all the good crystal like this having same mosaicity. Good cryo condition so far that I found was 10%Glycerol with mother liquor. Other conditions weekens the diffraction quality or increase mosaicity. In many crystal I could see some crack in the middle of the crystal, it looks like twin crystal. Or the crystal appears with some sattelite crystals. Can anyone suggest me some good way to overcome these problems. Thankz Sajid From Chandigarh to Chennai - find friends all over India. Go to http://in.promos.yahoo.com/groups/citygroups/ CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999 |
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