Hi all,
An NIH-funded postdoctoral position is available in the Department of
Biochemistry and Molecular Pharmacology at the University of Massachusetts
Medical School in Worcester, MA. Our multidisciplinary lab focuses on using
biochemical, structural, cell biological, microscopy and genetic s
Hi all,
So, I know this probably isn’t the right place, but I’m certain most of you
here have battled/fixed this issue. I just did a clean install of FC20 on an
AMD dual core system. I opted for the 32 bit version, as these workstations
are used for multiple things (and I find that it’s just
I have experience with some proteins that don't tolerate freeze-thawing
very well. It's hard to say exactly what the physical chemistry of this
is, but it probably relates to (1) aggregation due to high concentration
or protein or salts during the freezing process as water is removed,
and/or (2
Dear all,
I've encountered people who refuse to freeze cells and always lyse fresh
pellets. Better protein, they say. I've never had reason to do so
myself, or even to believe in their voodoo. Up until now, maybe.
My protein expresses well and is almost all in the soluble fraction in
an e
Hi,
This is way off topic but relevant. Does anyone routinely
use the Rainin Classic Pipet series? If so, what are your
thoughts and how often do they need to be calibrated?
Best wishes,
Reza
Reza Khayat, PhD
Assistant Professor
The City College of New York
Department of Chemistry, MR-1135
160
Hi,
Also, if you go from XDS to aimless with the INTEGRATE_ASCII.HKL or XDS_ASCII.HKL file, aimless has an option to omit batches (frames) as you wish from scaling or merging.
Boaz
Boaz Shaanan, Ph.D.
Dept. of Life Sci
Dear Almudena,
Doing two different runs (1-900 and 1001-1200) will do what you want. You will
have to do it from 2 different directories (called e.g. wedge1 and wedge2, or
whatever). With XSCALE you can merge the runs.
Best,
Herman
Von: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] Im Auft
Hi,
Another option to do it in xds (following advice of a Kay) is to rename the frames you don't like differently than the template.
Boaz
Original message
From: Almudena Ponce Salvatierra
Date:
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] XDS
Dear
Hi Almudena,
Greeting from Oulu.Other possibility would be, process the group of
Frames separately in XDS and merge them in the end.
Thank you
Rajesh
On Mon, Sep 29, 2014 at 12:56 PM, Almudena Ponce Salvatierra <
maps.fa...@gmail.com> wrote:
> Dear all,
>
> I would like to ask something
Hi Almudena,
if you run XDS through xia2, you can define multiple wedges in your info:
BEGIN SWEEP SWEEP1
IMAGE image_0001.cbf
DIRECTORY /path/to/files/
START_END 1 900
END SWEEP
BEGIN SWEEP SWEEP2
IMAGE image_0001.cbf
DIRECTORY /path/to/files/
START_END 1001 1200
END SWEEP
Andreas
On 29/
Dear all,
I would like to ask something regarding XDS. Is it possible, without
changing the Name of the Frames, to leave some out while processing?
i.e. something like defining twice the data range
DATA_RANGE= 1 900
!DATA_RANGE= 901 1000
DATA_RANGE= 1001 1200
Is there a way to do so? to leave ou
11 matches
Mail list logo