Hello everyone, I need your suggestion for slowing down crystallization for my
proteinmy protein got hit in PEG/ION #5 ( 0.2 M MgCl2, 20% PEG 3350, pH 5.9),
but it crystallize too fast. In 1 hr I can see tons of tiny needles. Can anyone
give me some suggestion on how to slow down the process? I
of excessive peptide in the solution?
someone suggested I use lot of peptide , say 3 times of the peptide to protein.
usually what is the ratio you will try when you deal with this not-so-small
ligand ?
any suggestion is appreciated.
Lei Feng
Sorry to bother those not interested.
could anyone share some information on the Free Electron Laser used for
crystallography in Stanford? I just heard from friend that they use this
extreme high intensity beam to shoot micro crystal.
anyone know those , could you please share some
hello everyone
can anyone recommend an affordable low temp. incubator that could be used for
crystallography?
we do not have cold room, so hope the incubator can go to 4 degree withouth too
much vibration
any size from 10 cubic ft --20 cubic ft will be fine
any help is highly
hello everyone
I really appreciate it if anyone can recommend a microscope for crystallography.
I am looking at manual one ( without any fancy motor driven stage or fancy
digital camera-computer stuff) , but need have the trinocular for a simple
digital camera to take photo
I was using
hello everyone
I am about to setup a 3D system for crystallography. right now I can only think
of coot and pymol software. so I might just go with Windows sytem, plus the
Nvidia 3D vision kit
I know there is a detailed list of hardware recommended. but are they
compatiblility issues?
hello everyone
I am wondering how to make covalent bond in coot, between a modified substrate
and regular protien residue
I can not figure out how to make the bond. Your suggestion is appreciated.
Lei
Hello Paul
I am wondering , do we need uninstall the previous version of coot to install
this?
thanks
_
Windows Live Hotmail is faster and more secure than ever.
I just downloaded the new CCP4 package and installed it.
comparing with the old version ( I used CCP4 6.0.2 on my windows xp computer
and finished my Ph.D projects.), I found the new version of coot is kind of
slow in moving to the next residue of the structure by hitting the space. Can
hello everyone, I am seeking help on a crystal decay problem
I got crystals of a protein , but it decayed very fast in syncrotron beam. From
the initial index, it is P222 space group, I need about 180 images, its initial
diffraction went to about 3 A, and after 70-80 images, it droped to
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