Dear CCP4 Community ,which program i should use in ccp4 backage to find how
many molecules in Asymetric Unit .All the bestAmr
Dear All,first i wish you nice weekend, then i wanna ask about formulation of
my own mother liquor, i want to optimize a condition containing 0.2m MgCl2,
0.1m Tris , PH 8; and 20% PEG6K as pricipitant. (PACT)the question is , should
i make a stock solution from every ingredient by dissolving it
Dear ccp4bb Community ,i hope this email finds you well, i am trying to do add
Zink and Copper to my Superoxid dismuase Enzyme by Coot , i encountered two
problems.1- after adding Zink and copper by place atom at pointer << other <<<
writing ZN OR CU then running Refmac5 , both atom is turned
http://www.alliancecorporation.com/gtjxdgki/dqtyk/psx/ycqd/uuens/fdcl/opzb.htm
Best regards, amro selem
Dear colleagues,
i hope every one doing well. i am trying to remove the 10x his tag , as i tried
to crystallize with the tag but i didn^t obtain crystals unless
some salt crystals , very small crystals and some precipitant. i want to use
factor 10a protease but i didn^t tried it before. this is
Dear colleagues,
i hope every one doing well. i am trying to remove the 10x his tag , as i tried
to crystallize with the tag but i didn^t obtain crystals unless some salt
crystals , very small crystals and some precipitant. i want to use factor 10a
protease but i didn^t tried it before. this is
Dear all ,
my job is to clone part of the gene already carried on pJC40 vector .i sent
this vector for sequencing . i made also squence
alignment, i have found only 97% identity . this mean about five nuclutides
are not matching with original sequence . when i made protein blast i
also found 4
Dear all,
i want to do structural homology but i am still beginner , could some one help
me to do it.is there are specific programs to do that or should i do it
manually ?
thank you
Amr
Hallo every one,
i am working on one enzyme who has sulphur bridge , is using 2 mercaptoethnol
or DTT during handling this protein for crystallography is not desirable .
best regards
Amr
hallo every body, i face problem with protein when i make gel filtration or
concentrate my protein . i notice sever aggregation . i use only glycerol as
additives to 50 mM TRIS and 150 mM NaCL ; PH 8 . my IP is 7.8 . any suggestions.
best regards
Amr
Hi all , thank you for being new member in this group. i also just stated with
my PhD in structural biology at Hamburg University (DESY) . i have no Idea
about crystallography . I just go step by step. so please help me to find my
way for excellence in structural biology. i appreciate your sugg
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