Hi,
three things come to mind besides what has been mentioned already
- many proteins that have an affinity for nucleic acids actually love sulfates
or phosphates… And yes, phosphates may lead to salt crystals at higher pH
values but this should not stop you a priori from screening with the sam
Hi,
cytochrome P450 (heme + nadp)
nitric oxide synthase (FAD, FMN, heme)
ferredoxin-NADP+ reductase
succinate dehydrogenase complex II (FASD + iron-sulfur)
ribonucleotide reductase (Fe + Mn + tyrosyl radical)
lactate oxidase (FMN + Ca)
glutamate synthase
dihydrooroate DH
Lipoamid DH
Xanthine oxida
Hi,
to me it looks like 2 things are happening in the drops, to many nuclei and on
these initial nuclei new crystals appear. This may indicate that your protein
is not that soluble to start with and that there may be some protein
aggregation going on in your protein stock solution. Diluting the
Hi,
compared to the M3, the upgrade is mainly about in the number of total cores,
ratio between efficiency vs performance cores (6 + 3 or 4), 10 instead of 8 GPU
cores, improved neural engine, increased maximum memory capacity (32GB) and 20%
increased memory bandwidth (now 120 GB/s). Same is tr
Hi Amit,
the questions and suggestions by Eta are important ones and I would like to
extend them a little bit.
For your apo crystals, instead of adding DMSO in one go, transfer the crystal
to a drop with 5% DMSO and wait, if it survives, transfer to 10%, to 20% and
finally to 30%.
Then, do no
7229
Office: 706-583-0304
Lab:706-583-0303
FAX: 706-542-1738
***
From: Jeroen Mesters
Date: Wednesday, June 5, 2024 at 1:17 PM
To: Zachary A. Wood
Cc: CCP4BB@jiscmail.ac.uk
Subject: Re: [ccp4bb] Ligand identification in X-ray density
You don
Original Message
On 05/06/2024 17:54, Jeroen Mesters
<cf8d8aa45b08-dmarc-requ...@jiscmail.ac.uk<mailto:cf8d8aa45b08-dmarc-requ...@jiscmail.ac.uk>>
wrote:
Thank you for this intriguing information!
At the same time, this also implies that not all entities that have
logy
University of Georgia
Life Sciences Building, Rm A426B
120 Green Street
Athens, GA 30602-7229
Office: 706-583-0304
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***
From: CCP4 bulletin board mailto:CCP4BB@JISCMAIL.AC.UK>>
on behalf of Jero
Hi,
proteins my pick up ligands from the „source" from which they were isolated….
Looks to me like trimethylglycine, an amino-acid derivative found in plants…
Regards,
Jeroen
__
https://orcid.org/-0001-8532-6699
Am 05.06.2024 um 17:44 schrieb Khadijah Ameen Khan
:
Dear All,
I am a first
Hi Mark,
Gentauer may still sell those…
https://maxanim.com/strains/m15-prep4-escherichia-coli-strains/
Cheers,
Jeroen
__
Dr. math. et dis. nat. Jeroen R. Mesters
Biological Safety Officer (BBS)
Deputy, Lecturer, Program Coordinator Infection Biology
Visiting Professorship in Biophysics South B
Do not know what the resolution is here, try an anisotropic refinement of the
Cys side chains first to see if this solves your problem.
__
Dr. math. et dis. nat. Jeroen R. Mesters
University of Lübeck
https://orcid.org/-0001-8532-6699
Am 06.05.2024 um 21:48 schrieb Eleanor Dodson
<176a9d
I am looking for coot-0.5.2-osx-universal.dmg.gz
Anybody out there that can help?
- J. -
mesters wrote:
> Sorry for the off-topic but can somebody recommend highly a sensitive
> RT-PCR machine for the thermofluor experiment (sypro orange).
> That would imply excitation below 500 nm (ideally 470) and detection
> at about 570 nm, right? I know several simple machines have a problem
> wit
Hi Gregor,
I think this LCD monitor is not useful since the refresh rate is only 75
Hz, thus in stereo 2 x 37.5 Hz and that is going to give a big headache.
I know Samsung is working on a 100 Hz LCD-TV. Nevertheless, the goal is
not for stereo but to suppress the afterglow effects again.
They tri
Dear Pedro,
there is no cheap solution for now, the 3D community has to wait for a
few years more I think to be presented with a good stereo-capable LCD.
The problem is not the refresh rate (as low as 5 ms nowadays) but it is
the after glow effect... that is one of the reasons why LCDs provide a
s
Hi,
if I recall this correctly, it is the nickel that is in your sample
after elution and boiling your protein in SDS sample buffer does the
rest.
So, could be the sample is fully okay!!!
J.
Tiago Botelho wrote:
> Hi,
>
> I also had a similar problem with one of my proteins... I had it clon
Venky,
have a look at your Xorg.config file in /etc/X11 directory.
Make sure to set the options correct (Option "Stereo" "3")!:
Section "Device"
BoardName"Quadro FX 3450"
BusID"1:0:0"
Driver "nvidia"
Identifier "Device[0]"
Option "IgnoreEDID"
Option "S
For Stereophiles and Xineramaphiles,
for those that asked me for our Xorg.config file (see below) for running a two
screen setup (requires Nvidia Quadro card).
This file is set up for a stereo beamer and a LCD.
You have to do some editing of your xorg.conf file (do that by creating
a copy and
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