Dear ccp4 community,
I'll soon start my own lab and together with other colleagues, would like to
establish a facility to do large scale insect cell culture for crystallography.
Has anyone had any experience with the wave bag systems for this purpose (for
instance from GE)? I have heard that
Dear Friduous,
This is also a good paper to look at once you know your crystals diffract at
room temperature:
https://www.ncbi.nlm.nih.gov/pubmed/10944336
Many of the salts in your condition will be cryo-protective if you increase
their concentration to saturated levels.
Cheers,
Joseph.
information of at least two references.
This should be sent to joseph.br...@ki.se and jesper.haeggst...@ki.se.
The deadline for application is the 22nd of June, 2017.
Joseph Brock | PhD
Division of Physiological Chemistry II
Department of Medical Biochemistry and Biophysics
Karolinska Institutet
to joseph.br...@ki.se and jesper.haeggst...@ki.se.
The deadline for application is the 28th of April, 2016.
Joseph Brock | PhD
Division of Physiological Chemistry II
Department of Medical Biochemistry and Biophysics
Karolinska Institutet
Scheeles väg 2
SE-171 77 Stockholm, Sweden
Ps - application deadline is the 13th of March, 2017.
Best,
-Joseph.
Joseph Brock | PhD
Division of Physiological Chemistry II
Department of Medical Biochemistry and Biophysics
Karolinska Institutet
Scheeles väg 2
SE-171 77 Stockholm, Sweden
From: Joseph Brock
Hi Elanor and bb,
I realised this was due to me creating a .HKL file with XDS from Eiger data
with a DATA_RANGE that was not a multiple of 50!
Apologies for any trouble!
All the best,
Joseph.
Joseph Brock | PhD
Division of Physiological Chemistry II
Department of Medical Biochemistry
seInRuns::apply Unused run 0"
#CCP4I TERMINATION TIME 21 Jan 2017 00:18:31
#CCP4I MESSAGE Task failed
Thanks in advance for the help.
Cheers,
Joe.
Joseph Brock | PhD
Division of Physiological Chemistry II
Department of Medical Biochemistry and Biophysics
Karolinska Institutet
Scheeles väg 2
Hi Suda,
You can do this in Coot by loading the two structures, then using the tool
Calculate- SSM superpose.
The rmsd value and sequence identity should be reported within your terminal
window.
Hope that helps.
-Joe
Date: Thu, 18 Aug 2011 14:40:32 +0530
From: biobud...@gmail.com
Hi everyone,
I have two conditions that I want to try and improve by microseeding. I have
been reading the literature on the subject and am a bit confused as to what
exactly is the stabilizing mother liquor that is used in the serial dilution
of the seed stock. Is this just purified protein