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.
and a CV with publication list.
Contact details of two references should also be provided. Send the application
as an email with attachments to martin.hallb...@ki.se
Review of applications will begin immediately and continue until the position
is filled.
.
B. Martin Hallberg, PhD
Department of Cell
Hi,
Can you explain what you want to do?
Do you just want more of some tRNA corresponding to a codon that is rare in E.
coli you can use the pRare2 plasmid that you can easily isolate from the
Rosetta2 strain (or use Rosetta2 directly if you don't mind).
If you just want some extra tRNA
I think it is still hard to beat lsq_imp as implemented in 'O'.
http://xray.bmc.uu.se/alwyn/A-Z_of_O/everything_e-l.html#anchor1342614
Cheers,
Martin
On Nov 15, 2010, at 2:32 AM, Clement Angkawidjaja wrote:
DALI server (http://ekhidna.biocenter.helsinki.fi/dali_server/). Choose the
Dear Sergei,
Did you check the mean intensity as function of spindle position statistics
in the CORRECT.LP file?
Any (even minute) shutter problems will affect these thin frames significantly.
If this is indeed the problem, you could then try to set:
PATCH_SHUTTER_PROBLEM=TRUE
for the CORRECT
in XDS (which should have no problems with fine phi-slicing) to use the
PATCH_SHUTTER_PROBLEM=TRUE that Martin Hallberg suggested, which looks a
bit like a fudge to me (but I expect Kay to correct me on that!).
It is not the normal thing in XDS but it is perhaps a relatively common
solution
it.
Matthew Vetting
.
Martin Hallberg, PhD
Department of Cell and Molecular Biology
Karolinska Institutet
Stockholm
Sweden
http://tinyurl.com/yzn9y5j
Hi Tommi,
In S. cerevisiae you need a sam1(-) sam2(-) mutant. You can contact the
authors of the paper in this link to get them:
http://www.pnas.org/content/104/16/6678.long
Cheers,
Martin
On Oct 5, 2010, at 3:47 PM, tommi kajander wrote:
Hello all,
Would anyone happen to have a met
Dear Hannes,
I am afraid it can still be phage problems. There are many kinds of phages that
infect E. coli and some of them behave like you describe: not always
lysed cells but from time to time and coming and going. The phage may anyway be
present
but in its lysogenic state and only entering
BTW, has anyone tried out the higher resolution 24 inch 3D model from Zalman
that appears to be available
from this reseller in Japan?:
http://mikimoto-japan.com/beans/products/product_dsp.htm
and this reseller in the UK:
http://www.cleverpc.co.uk/index.php?productID=5338
My guess it that it is
a cover letter and a CV with publication list.
Contact details of two references should be also provided. Send the application
as an email with attachments to martin.hallb...@ki.se
Review of applications will begin immediately and continue until the position
is filled.
.
B. Martin Hallberg, PhD
is less than 1.1.
I have in the past been comforted by this statement by George...
You can also try the SHELXWAT module.
Cheers,
Martin
.
Martin Hallberg, PhD
Department of Cell and Molecular Biology
Karolinska Institutet
Stockholm
Sweden
http://tinyurl.com/yzn9y5j
On Nov 12, 2009, at 8:53
Hi,
On Jun 25, 2009, at 6:41 PM, Ian Tickle wrote:
But I thought what you wanted was to reconstruct the diffraction
pattern
(i.e. streaks, TDS, ice rings, zingers, warts all) as a
pseudo-precession image, not just display a representation of the
integrated intensities. That surely would be
. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Karolinska Institutet
von Eulersv. 1
SE-171 77 Stockholm
Sweden
Fax: +46-8-339380
Hi,
Have you specified the right form factor for Se given
the wavelength used in your experiment?
anomalous formfactor [Name] [f'] [f'']
You can also try the new option where you can do simultaneous
SAD phasing and refinement. See: http://tinyurl.com/8on2cr
You will have to upgrade from your
phone: +1 604 827 4267
email: [EMAIL PROTECTED]
http://crg.ubc.ca/VanPetegem/
.
B. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Medical Nobel Institute
Karolinska Institutet
Von Eulersv. 1
SE-171 77 Stockholm
Sweden
Fax: +46-8-339380
a try to carefully collect a
data set using a wavelength around 1.5-1.6 Å (or simply your home
source depending on how good it is).
Cheers,
Martin
.
B. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Medical Nobel Institute
Karolinska Institutet
Nobels väg 3
SE
and/or spatially overlapped
macromolecular diffraction patterns.
by Dominique Bourgeois.
Link: http://scripts.iucr.org/cgi-bin/paper?BA0019
Best regards,
Martin
.
B. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Medical Nobel Institute
Karolinska Institutet
. Dodson).
Why I'm worried about XDS separating relatively overlapped spots is
the funny intensity stats that may result from this (as George
Sheldrick and Martin Hallberg has pointed out)? The incomplete
HKL2000-processed data (70%) still has intermediate values for the
intensity stats
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 with the 570 nm...
Jeroen.
.
B. Martin Hallberg, PhD
Assistant
precipitation.Also
appreciate worth suggestions from groups working with
chaperonins.Thanx in advance.
Shivesh kumar
.
B. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Medical Nobel Institute
Karolinska Institutet
Nobels väg 3
SE-171 77 Stockholm
Sweden
try to make a seed stock and then a dilution series of that.
Good luck!
Martin
.
B. Martin Hallberg, PhD
Assistant professor
Department of Cell and Molecular Biology
Medical Nobel Institute
Karolinska Institutet
Nobels väg 3
SE-171 77 Stockholm
Sweden
Institute
.
B. Martin Hallberg, PhD
Molecular Cell Biology Program
Department of Cell and Molecular Biology
Karolinska Institutet
SE-171 77 Stockholm
Sweden
diffraction from one, 2, 3 an array of
objects?
Cheers, br
Bernhard Rupp
www.ruppweb.org
.
B. Martin Hallberg, PhD
Molecular Cell Biology Program
Department of Cell and Molecular Biology
Karolinska
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