DNA purification

[schupp at nauvax.ucc.nau.edu]

There's a short article in the October issue of Biotechniques concerning just
this.  The technique involves running the target DNA on regular agarose for
separation, then taking a plug of agarose from one side of the band with a
pasteur pipet.  The gel is then rotated 90 degrees and the dna electrophoresed
into the buffer filled hole.  The authors claim 60-80% recovery. Hope this
helps.