A.
Secondary
> Structure prediction suggest a lot of beta strands. How can I explain the
> anisotropy (for my own interest and my thesis)?
> Thank you very much.
>
> Marie
>
>
>
--
***
Jose Antonio Cuesta-Seijo
Biophysical
Chemistry Group
Department of Chemistry
University of Copenhagen
Tlf:
+45-35320261
Universitetsparken 5
DK-2100 Copenhagen,
Denmark
***
n and
reduce
> the quantity of protein found in inclusion bodies?
>
> Thanks! and all the best,
>
> --Buz
>
--
***
Jose Antonio Cuesta-Seijo
Biophysical
Chemistry Group
Department of Chemistry
University of Copenhagen
Tlf:
+45-35320261
Universitetsparken 5
DK-2100 Copenhagen,
Denmark
***
end up mostly in the reservoir leaving onlt traces in the drop, while the
cholesterol will stay in the water. It might precipitate at first, but
should redissolve or not precipitate at all if it binds your protein.
Jose Antonio Cuesta-Seijo.
"Jerry McCully" wrote:
>
the crystal by plunging it in liquid Nitrogen, so the final
concentration of isopropanol in the loop will be higher, which increases
the chances of not needing any extra cryoprotectant.
Jose Antonio Cuesta Seijo.
herman.schreu...@sanofi-aventis.com wrote:
> Dear Chris,
>
> I recall
Fourier ripples. These will be particularly strong around
regions of high density, such as heavy atoms."
Jose Antonio Cuesta-Seijo.
"Franck borel" wrote:
> Dear all,
>
> We have a structure with triiodothyroninne (T3 hormone) in it. The
> density around the ligand
I would like to add that contrary to popular belief, MPD would have to be
treated as a volatile in the example you give below. It vaporizes, although
very slowly, as can be proven by leaving a 1uL drop of it in open air for a
couple of days.
Cheers,
Jose Antonio Cuesta Seijo.
"Jacob K
between the
main chain and the side chain of LYS181. Similar examples are all over the
1000+ residues in this structure.
Is this normal? All global quality indicators look OK to me...
Cheers,
Jose Antonio Cuesta Seijo.
ATOM 8338 N ARG F 178 65.398 30.884 -0.261 1.00
84.90 N
y the point where you
> don't have enough strong reflections for robust refinement of
> parameters. The absolute values will, of course, vary from dataset to
> dataset.
>
>
> --
>
--
***
Jose Antonio Cuesta-Seijo
Biophysical
Chemistry Group
Department of Chemistry
University of Copenhagen
Tlf:
+45-35320261
Universitetsparken 5
DK-2100 Copenhagen,
Denmark
***
am in Molecular Medicine
> Biotech II, 373 Plantation Street, Suite 115
> Worcester MA 01605
> Phone: 508 856 1201 (office); 508 856 1211 (lab)
> e-mail: bert.vandenb...@umassmed.edu
> http://www.umassmed.edu/pmm/faculty/vandenberg.cfm
>
>
> "Parvee
Has anybody seen DDM crysals
and
> if yes, how do they look like?
>
> thanks in advance
>
> Parveen Goyal
>
--
***
Jose Antonio Cuesta-Seijo
Biophysical
Chemistry Group
Department of Chemistry
University of Copenhagen
Tlf:
+45-35320261
Universitetsparken 5
DK-2100 Copenhagen,
Denmark
***
that conditions that
give ordered iodide sites are likely to result in ordered bromide
sites, although the ions are not identical.
Jose.
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRS TMDT Room 4-902M
101 Co
hanks,
Jose.
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRS TMDT Room 4-902M
101 College Street
M5G 1L7 Toronto, ON, Canada
Phone: (416)581-7544
Fax: (416)581-7562
email: jcue...@uhnres.utoronto.ca
**
bel Institute
Karolinska Institutet
Von Eulersv. 1
SE-171 77 Stockholm
Sweden
Fax: +46-8-339380
--
Wangsa Tirta Ismaya
=============
Josef-Israelstraat 66, 9718 GN Groningen
The Netherlands
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute
sed on one case, but your case is s similar to mine!
Good luck,
Jose Antonio Cuesta-Seijo.
******
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRS TMDT Room 4-902M
101 College Street
M5G 1L7 Toronto, ON, Canada
Phone:
ot;, what are the physical and
chemical underlying problems?
Can they be used at low concentration without damaging the matrix or
abolishing binding?
Which are the maximal concentrations people had success with?
Thanks a lot,
Jose Antonio Cuesta Seijo
**********
Jo
time finding any details or protocols.
I bet that there is a lot of anecdotal experience out there. Maybe
even references?
Thanks,
Jose.
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRS TMDT Room 4-902M
101 Co
, that is, SCBUlk 0.2 produces the
same results as SCBULK -0.2
What is the excat meaning/use of those parameters?
How are the experts going around with optimizing these?
Thanks,
Jose Antonio Cuesta Seijo.
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and
And here some more small molecule crystallization links.
http://xray.chem.ufl.edu/growing%20tips.htm
http://mic.ucla.edu/x-ray%20diffraction/tutorials_crystalgrowing.htm
http://www.nottingham.ac.uk/~pczajb2/growcrys.htm
Jose Antonio Cuesta-Seijo
On Jul 18, 2007, at 5:56 PM, Green, Todd wrote
ic/linkfiles/
Crystallisation_Techniques.doc
Good luck,
Jose.
******
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRs TMDT Room 4-902M
101 College Street
M5G 1L7 Toronto, On, Canada
Phone: (416)581-7544
Fax: (416)581-7562
email: [EMA
.
Jose.
**
Jose Antonio Cuesta-Seijo
Cancer Genomics and Proteomics
Ontario Cancer Institute, UHN
MaRs TMDT Room 4-902M
101 College Street
M5G 1L7 Toronto, On, Canada
Phone: (416)581-7544
Fax: (416)581-7562
email: [EMAIL PROTECTED
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