Renaud renaudleo at
Mon Oct 5 02:22:12 EST 1998

I would like to realise a native PAGE electrophoresis. The protein I want
to purifie has an isoelectric point at 9.5. The buffers I have used have
an isoelectric point at 7.7 and 8.7 so I have inverted the polarities
during the migration. My probleme is that my protein stays in the well.

Thanks to answer at : renaudleo at

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