For the separation of macromolecules by either size or surface electri
cal charge density, gel electrophoresis is a technique used in all are
as of biochemistry. For the analogous separation of larger, multimolec
ular particles such as viruses, gel electrophoresis has more recently
also been found useful. As the radius of a spherical particle exceeds
200 nm during electrophoresis, a phenomenon that defines a larger sphe
re occurs: the normally used electrical fields cause large spheres to
be sterically trapped in the network of gel. Either pulsed or comparat
ively low electrical fields are introduced to either overcome or utili
ze trapping during the gel electrophoresis of large particles.