Dear All,
we have two data sets at about 0.9 and 1.9 Ang. resolution collected from a
single crystal.
Integration with iMosflm seems to be fine like the scaling within each of
the data sets.
When we try to merge and scale both of them with 'Scala' we get extremely
high scale factors for the
Hi All,
does anyone in macromolecular crystallography have any experience with
STOE apparatus and in particular with their STADI VARI goniometer and
PILATUS 100K detetor?
Thank you
Kyriacos
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