A large-scale preparative polyacrylamide gel electrophoresis (PAGE) sy
stem for the isolation of high-purity supercoiled plasmid-DNA is descr
ibed. This method should prove suitable for the isolation of large DNA
molecules, either plasmid or linear DNA, that is required for the pro
duction of transgenic animals, for instance. The efficiency of the met
hod is illustrated by the isolation of the gene for the green fluoresc
ent protein, cloned into a mammalian expression vector and used for tr
ansfection of eukaryotic cells.