Mini-S is not quite what you're looking for. It's 3uM particles and has a
nice fat back pressure. Resource S-15 and Resource S-30 (with 15uM and 30uM
average particle size) may be what you need.
You may also want to take a look at monolithic columns because they develop
a lot less back pressure th
Dear Hudel,
I have Zalman monitors M215W connected to an iMac and to a PowerMac and
both pymol and coot work well. I also tested the monitors in my MacBook
pro and they work fine. The MacBook pro has an NVIDIA GeForce GT 330M,
the iMac has an ATI Radeon 5750 and the MacPro has ATI radeon 5770.
Postdoctoral Position - Structural & Cell Biology
The Scripps Research Institute in La Jolla, CA
A Postdoctoral position is available to study the structure and function of
protein-protein interactions involved in tumor growth. The position requires a
recent Ph.D. in one of the natural sciences
Hi,
"Indonesia" is great for this.
http://xray.bmc.uu.se/dennis/
Cheers,
Martin
On Jan 25, 2011, at 10:50 PM, Katherine Sippel wrote:
> Hi all,
>
> I was wondering if you know of a program that can do protein sequence
> alignments around experimentally determined equivalent residues (i.e.
Hi all,
I was wondering if you know of a program that can do protein sequence
alignments around experimentally determined equivalent residues (i.e.
biochemists have determined via mutagenesis and kinetics that residues 3,6
and 9 of protein X are the equivalent of residues 7, 14, 21 in homologous
p
Hi Jonas,
a Mini S has a even lower bead radius of 5 µm, if I remember correctly. Its
available as prepacked column from GE. I have a 1 ml column which is quite
expensive. i guess you won't spent such an amount of money. It is also more
for analytical purposes and not preparative scale. Never h
Dear All,
I am currently looking into various cation exchange resins for the separation
of mono-, di-, tri-, tetra-,... ubiquitin. So far I have been using a small
Mono S column but would ideally like to both scale up and increase resolution.
Before I started searching for this online I have nev
I think the likely reason here are the points where you did the
mutations having adverse effects
- how do the mutants behave without labeling? this would be of course
an important control...
-Tommi
On 25.1.2011, at 12.52, Paula Salgado wrote:
Dear Abhilash
You could try an alternative la
Dear Abhilash
You could try an alternative labelling option: if your protein has
cysteines, try labelling those with selenium. We succeeded in doing this
using non-auxotrophic strains, meaning you deviate less from your native
expression protocol and are therefore more likely to obtain well folded
Dear All,
I am working on structure determination of a bacterial protein. The protein was
expressed as a GST fusion protein in E. coli. I got crystals of the native
protein.
I am trying to label my protein with Se-Met.
The purification protocol involves GST affinity purification, cleavage of the
On 25 Jan 2011, at 08:35, Harry M. Greenblatt wrote:
> Has someone received an official answer from NVIDIA that they do *not* work?
I raised this issue here back in November. Someone, whose email I cannot now
find, replied off-list to say that they had been told by nVidia that 3D Vision
did no
BS"D
According to the NVIDIA website, the Mac versions of the Quadro FX
4800 and the Quadro 4000 have 3 pin stereo ports, and there is
nothing that I could find that says that the MAC drivers for these
cards don't support quad-buffered stereo using the new LCD screens
and NVIDIA glasses
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