A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization

Walter, T.S.; Diprose, J.M.; Mayo, C.J.; Siebold, C.; Pickford, M.G.; Carter, L.; Sutton, G.C.; Berrow, N.S.; Brown, J.; Berry, I.M.; Stewart-Jones, G.B.E.; Grimes, J.M.; Stammers, D.K.; Esnouf, R.M.; Jones, E.Y.; Owens, R.J.; Stuart, D.I.; Harlos, K.

doi:10.1107/S0907444905007808

Acta Crystallographica Section D
Acta Crystallographica
Section D BIOLOGICAL CRYSTALLOGRAPHY

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Figure 6
Web interface. (a) Pixera images of protein crystal, (b) salt crystals grown from the same condition, (c) time course of drop D08, (d) montage of all 96-well images taken in one session, (e) single-well image of drop D8 with user options. Images of protein crystal used with permission (Aricescu et al., unpublished).

BIOLOGICAL
CRYSTALLOGRAPHY

ISSN: 1399-0047

Volume 61| Part 6| May 2005| Pages 651-657

doi:10.1107/S0907444905007808

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