Hi everyone,
I wonder if I can add PEG or Li2SO4 into protein sample for new screen?
Because optimization seems no good result, initial crystal was got in
Bis-Tris, PEG8000, Li2SO4. If it is OK, then what's the concentration of
PEG or Li2SO4?
Best regards,
Shiqing
Hi, Shiqing,
In my opinion, it is not good idea.
If you want to optimize the protein buffer than you could look at
thermofluor method of protein buffer optimization.
BTW, have you tried seeding?
03.06.2013 10:56, Qing Shi ?:
Hi everyone,
I wonder if I can add PEG or Li2SO4 into protein
Hi,
If anyone fancies becoming Life Science Director at the world's brightest light
source, look no further than here:
http://www.lunduniversity.lu.se/o.o.i.s?id=24914Dnr=547454Type=E
/Derek
Derek Logan
Brighter than XFEL? Or is it going to be an XFEL?
JPK
On Mon, Jun 3, 2013 at 10:36 AM, Derek Logan derek.lo...@biochemistry.lu.se
wrote:
Hi,
If anyone fancies becoming Life Science Director at the world's brightest
light source, look no further than here:
-BEGIN PGP SIGNED MESSAGE-
Hash: SHA1
Probably brighter than an XFEL if you average over a reasonable amount
of time greater
than fs ;-)
Tim
On 06/03/2013 05:13 PM, Jacob Keller wrote:
Brighter than XFEL? Or is it going to be an XFEL?
JPK
On Mon, Jun 3, 2013 at 10:36 AM, Derek
Thanks Tim! But seriously, MAX IV will, as well as being a synchrotron, have a
Short Pulse Facility at the end of its linac:
http://www.maxlab.lu.se/femtomax
By world's brightest light source of course I loaned a management slogan, but
MAX IV will be a 3 GeV facility with emittance around 0.25
