Jilge G, Unger K K, Esser U, Schäfer H J, Rathgeber G, Müller W
Institut für Anorganische Chemie und Analytische Chemie, Johannes Gutenberg-Universität, Mainz, F.R.G.
J Chromatogr. 1989 Aug 4;476:37-48. doi: 10.1016/s0021-9673(01)93854-3.
The linear solvent strength model of Snyder was applied to describe fast protein separations on 2.1-micron non-porous, silica-based strong anion exchangers. It was demonstrated on short columns packed with these anion exchangers that (i) a substantially higher resolution of proteins and nucleotides was obtained at gradient times of less than 5 min than on porous anion exchangers; (ii) the low external surface area of the non-porous anion exchanger is not a critical parameter in analytical separations and (iii) microgram-amounts of enzymes of high purity and full biological activity were isolated.