stem had a glitch, and
there was no X-ray. True story!
Best wishes
-Z
Zaigham Mahmood Khan, PhD
Icahn School of Medicine at Mount Sinai
Department of Oncological Sciences
1470 Madison Avenue
New York
On Tue, Aug 14, 2018 at 5:58 AM, Careina Edgooms <
02531c126adf-dmarc-requ...@jiscmail
s..
Best wishes
-Z
Zaigham Mahmood Khan, PhD
Icahn School of Medicine at Mount Sinai
Department of Oncological Sciences
1470 Madison Avenue
New York
On Fri, Jul 6, 2018 at 5:42 AM, Wim Burmeister
wrote:
> Hello,
> a really molecule should show up also in the 2Fo-Fc type map. This appears
...
Best wishes
-Z
Zaigham Mahmood Khan, PhD
Icahn School of Medicine at Mount Sinai
Department of Oncological Sciences
1470 Madison Avenue
New York
On Mon, Jul 2, 2018 at 10:23 PM, Uma Gabale <
0ebb5dcf3eaa-dmarc-requ...@jiscmail.ac.uk> wrote:
> Dear all,
>
> We came a
hey Liu
... you got all wonderful suggestion, and they may be time consuming.
Meantime, you may work on the crystals in hand, and follow the suggestions
as mentioned above.
>From my experience, i can tell you that crystal age is also an important
parameter. I will shoot it as soon as i see it in
d different kinds of cryoprotectants that have
been successfully attempted in the past. Off-course, this also depends on
type of precipitant that you used for crystallization. Apparently, this
seems as glycerol worked better in your case, may be because you have
salt-based precipitant.
Best wishes
Hey Firdous
Yes, too much information can be confusing. I have expressed and purified
over dozen of different proteins. I usually found in literature the
protocol for the expression and purification of another homologous protein.
That is the best way to start in my opinion. Some folks may want to
sult section, and from pdb.org, you may
find the residues of that protein that were observed in the electron
density map as well as whole expression casstte that was attempted to
crystallize for that particular pdb entry.
Best wishes
-Z
Zaigham Mahmood Khan, PhD
Icahn School of Medicin
Hey Anamika
I know SH2 domain is very much well-studied domain, and i am not sure why
are you facing troubles in the expression of this protein. Just go through
the literature and read about different protocol of expression of SH2
domain from several different proteins.. Well, reading that you hav
This may seem an interesting case, given that protocol fur purification,
and subsequent crystallization is reproducible as well as this enzyme is a
valid drug target for pathogenic strains of E. coli.
Best
Z
On Apr 5, 2017 02:51, "Vipul Panchal" wrote:
> I don't think it is going to be any scien
!
-Z
Zaigham Mahmood Khan, PhD
Icahn School of Medicine at Mount Sinai
Department of Oncological Sciences
1470 Madison Avenue
New York
On Mon, Apr 3, 2017 at 6:30 AM, Noam Adir wrote:
> Dear Supta,
>
>
>
> If I may make another type of suggestion, we have had success in
> cryst
keeping
protein concentration below 3 mg/ml solved the issue.
Best wishes
-Z
Zaigham Mahmood Khan, PhD
Fox Chase Cancer Center
ICR R428
333 Cottman Avenue
Philadelphia, 19111 PA
Phone: 215 728 3609
On Sat, Dec 24, 2016 at 2:55 PM, Kevin Jin wrote:
>
>
> Likely, the protein is pH
Yes, Eleanor D. is right. I had a similar experience. MR did not provide me
the solution with monomeric protein. However, when i used dimer as a search
model, it appeared to be a low-hanging fruit afterwards. May be you have a
similar situation, there are very less possibilities to explain othewrwi
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