Hi All
I am trying to code gene prediction. I am looking for the consensus pattern for
transcription start site, pribnov bow, ribosomal binding site and so on. I am
looking some pattern which are variable and I could not make any conclusion. If
anyone can provide all consensus pattern for
Dear All
I am running Linux CentOS in my system. Recently I installed latest version of
coot on my system. After successful installation, I restarted the system. But
failed to recover Xserver screen. I was trying to restart Xserver from command
mode but failed with following error message.
Dear Friends
I am looking for the provider details of instrument - Byron Bender (or super
protein wire model bender), which is used to build protein wire model using
Torsion angle for teaching purpose. I could not find any such provider.
I greatly appreciate your help
Thank you
Dr. B. Syed
Hello All
I am interested in cloning a gene from a plant. I searched the database only
partial sequence is available, ie: for 160 residues only. The full length of
the protein is around 570 residues. I designed forward primer and I have no
clue to design reverse primer.
Any help
Thank you
Hello All
I am using CM Sephadex C50 column for my protein. I equilibrated column with
MOPS buffer pH 6.0. But during elution I am using only NaCl2. This looks like
changing the bed height. Before starting elution the bed height was around
60cm. After starting elution the bed height decreased
In my practice, I never worried about the skin. You need extra care while you
mount the crystal. In my case I have used the skin to mount my crystals without
any problem. In fact it was much helpful. While mounting, you should not take
the crystal covered with the skin.
Best
Syed
Dear All
Sorry to bother you by writing about CNS here. I am trying to contact Brunger
to get the downlad information throguh my official id. Yet I am not getting any
response. Could any one help?
Thanks in advance
Syed
Andre
I had same kind of crystal like in your picture. It diffracted around 2.7A.
Even I had some crystals where one end was closed. Both hollow crystal or the
closed end (part) crystal diffracted same.
With regards
Syed
--- On Thu, 6/3/10, Andre Ambrosio andre.ambro...@cebime.org.br
Hi
I have succeeded by using oil (such as parafin oil ... etc ) at reservoir on
top of the reservoir solution. You have to try several trials to find optimum
ratio.
With regards
Syed
--- On Thu, 5/6/10, zq deng dengzq1...@gmail.com wrote:
From: zq deng dengzq1...@gmail.com
Subject:
Hi All
I had two crystals grown in same well, one is small and other is 10 times
bigger. I treated both crystal in same cryo and same time. The smaller one
diffracted to 2.5A and the bigger one to 6-7A. I was expecting the bigger one
to diffract high resolution.
I assume the bigger crystal
, 2010, at 5:36 PM, syed ibrahim wrote:
Hi All
I had two crystals grown in same well, one is small and other is 10 times
bigger. I treated both crystal in same cryo and same time. The smaller one
diffracted to 2.5A and the bigger one to 6-7A. I was expecting the bigger one
to diffract high
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