Dear Markus,
I've had to solve this exact issue in the past. Putting a 'simple' (nothing
is simple these days, everything has some kind of AI or other evil gnomes
in it) spectrofluorimeter into the cold room *should* be OK.
Caveat #1: I don't know if this will work with your specific device
Cavea
Happy to do it!
All the best,JP
On Friday, July 26, 2024 at 12:28:22 PM CDT, Renuka Kadirvelraj
wrote:
Hi John,Thanks again for helping us! Regarding the map after placing missing
residues and refinement: you are correct, both the negat
I think you are right, in the final equilibrium all the moisture would condense
on the (evaporator?) coils, and there should be provision for them to drip into
a reservoir outside. However each time the door opens and humid air is
admitted, there will be condensation everywhere. If you leave th
Hi John,
Thanks again for helping us! Regarding the map after placing missing residues
and refinement: you are correct, both the negative and positive densities have
gone away from the loop.
Thanks,
Renu
-
Renu Kadirvelraj, Ph.D.
Research Scientist
A42
Hi Renu, how do the maps look (2Fo-Fc and Fo-Fc) after you run a standard
refinement in Phenix with the missing residues in place? If the negative
density disappears in the Fo-Fc then there is not necessarily a problem. Of
course the positive density should also go away in the Fo-Fc map since i
Dear All,
apologies for the off-topic question. I am facing the problem of running
enzyme activity assays at low temperature (close to 4C would be ideal) in a
fluorescence plate reader. Before I get labeled in our department as "the
one who voids warranties" and destroys our beloved plate reader, I
Dear all,
We would like to inform you that the rolling call for proposals for beamtime at
MX beamline P11, PETRA III is open.
Proposals to beamlines participating in the rolling procedure can be submitted
exclusively via this new access route. Submission is possible at any time
without a deadl
Dear members of the structural biology community,
I am looking for postdoctoral researchers and would be grateful if you could
bring the following position to the attention of potential candidates.
Thanks, Albert
Postdoc positions in the laboratory of Albert Weixlbaumer available at the
IGBM
We are pleased to announce that applications are now open for the 11th
joint Diamond-CCP4 Workshop on MX data collection and structure solution!
Bringing together leading experts in the field of MX to teach best practice
in data collection and analysis, this course is aimed at PhD students,
postdoc
Hi Eleanor,
I had basically the same question that I asked in phenixbb recently, the answer
was also that the reason for red blobs is the solvent mask. In phenix there is
mosaic modelling available that deals with the red blobs:
https://onlinelibrary.wiley.com/doi/full/10.1002/pro.4909
Best,
Hi Eleanor,
My understanding about negative holes in difference maps is that it is down to
incorrectly modelled bulk solvent. I have seen this in structures where there
are voids inside a protein that are perhaps in reality empty, but get modelled
as bulk solvent, and so you get a negative diff
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