Shibusawa Y, Ito Y, Ikewaki K, Rader D J, Brewer H B
Laboratory of Biophysical Chemistry, National Heart, Lung, and Blood Institute, Bethesda, MD 20892.
J Chromatogr. 1992 Apr 3;596(1):118-22. doi: 10.1016/0021-9673(92)80212-d.
Lipoproteins were separated by counter-current chromatography using the type-XLL coil planet centrifuge. The separation was performed with a polymer phase system composed of 16% (w/w) polyethylene glycol 1000 and 12.5% (w/w) dibasic potassium phosphate by eluting the lower phase at a flow-rate of 0.5 ml/min. About 5 ml of the sample solution containing approximately 150 mg of a lipoprotein mixture were loaded. High- and low-density lipoproteins were resolved within 12 h. Each component was detected by gel electrophoresis with oil red staining.