Hi, Dear all,
Firstly ,I'd like to thank all the people for their kind help,
especially Miguel, Bernie ,Mark, Moody, Eleanor, Eaton , Peter and
lots of others Without your help, I wouldn't make it this far.
Secondly, I'd like to share some of the experiences. We had a hard
time trying to do
To add to your survey:
Yes I have tried it. Yes it does work better for glassifying cryobuffers.
I saw Rob Thorne give a talk on this some time ago and immediately went
home to give it a try. I used a cryobuffer (25% (v/v) glycerol; 0.6N
NaOH; 25 mM SeMet) I had been having hit-or-miss
Dear all
I am trying to crystallize one DPC bound small peptide.Small cystals are
appearing.How can I grow it bigger for mounting.Any suggestions are
welcome.Thanx in advance.
Shivesh
Dear Taiana,
thy the updated info according to the new sfcheck style in:
http://www.ysbl.york.ac.uk/~alexei/sfcheck.html
or simply type sfcheck -h
What worked for me recently (and also described in the link above) was simply
typing
sfcheck -f mydata.mtz -m mymodel.pdb -omit 2 -map
you will
