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[ccp4bb]: glycosylation



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Here a rather not so crystallographic question for the weekend:
If I'm running a 40 kDa protein with an added glycosylation of about 20
kDa on a gel filtration/permeation column (Superose 6 or Superdex
etc...) do I expect the protein to behave more like a 60 kDa protein or
more like a 40 kDa protein.
I wonder if anybody has experience with the migration of glycosylated
proteins in gel filtration.
Any hints are much appreciated.
Many thanks
Yves
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Yves Muller
Department of Biochemistry
School of Biological Sciences                 Phone: +44-(0)-1273-678515

University of Sussex                          Fax:   +44-(0)-1273-678433

Falmer, Brighton BN1-9QG                   E-mail: y.muller@sussex.ac.uk

UK                http://www.biols.susx.ac.uk/faculty/biochem/muller.htm

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