It is an absolute pain!
do you mean you have residue 1 A 1A 2A 2A 3A 3A etc where they should be
numbered 1 2 3 4 5 6 A?
or should it be 1A 1B 2A 2B 3A 3B etc?
Eleanor
William Scott wrote:
Hi folks:
I am hoping there is a simple answer I have overlooked to the
following question. I have
Dear All,
In order to help calibrate some internal parameters in MOSFLM, I would
greatly appreciate a dataset of images collected on an R-axis HTC from
a well diffracting sample (such as lysozyme, insulin etc) on a
laboratory source. Ideally I would like a complete dataset, preferably
collect
Applications are invited for two open positions in the laboratory of Haixin Sui
in the Wadsworth Center, Albany, NY. One opening is for a postdoctoral fellow
starting in September of 2008. The other is for a Ph.D. student starting in
the spring or fall of 2009. These are funded positions adm
Many thanks to those who offered datasets, I think that I am well set
up now.
Thanks again,
Andrew
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 abo
How about 90?
If it is ok , maybe you need more than 3 or more xtals to collect the
whole dataset and merge them together.
Otherwise your xtals should be the anisotropic .You'd better to collect
images in the better region or screen more xtals to get better ones.
Good luck!
leo
lei feng wrote:
I'd rather go for a complete low resolution dataset. Is this a native
crystal ? HA derivative ? Even with a 4Å data set you can do something
it's painful but not impossible e.g. molecular replacement if
possible. Then at least you would know your spacegroup & perhaps gain
some insights from
