stugerNOstSPAM at cellbiology.uni-frankfurt.de.invalid
Fri May 26 03:24:29 EST 2000
I'm using pBR as a supercoiling reporter. In my recA+ strain,
the plasmid sometimes forms dimers, which are about 8 kbp.
Although individual topoisomers are visible in the 8 k dimer,
differences in supercoiling between different samples are hard to
But you might give it a shot with low % gels and/or long run
times. With such a big plasmid the range of possible topoisomers
may be very wide, tho. So if you can use a smaller plasmid I
would try that first.
Mol Cell Physiol, Free U of Amsterdam
E rogier AT bio.vu.nl
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