Abstract
Soluble rat liver cell proteins have been separated by electrophoresis on filter paper (1, 2) cellulose acetate (3), and starch gel (4) and by the Tiselius method (5). Although each of these approaches has its disadvantages, the main problem with cellulose acetate is drying of the strips during sample application and electrophoresis at higher voltages. Recently, a new type of gelatinized cellulose acetate, Cellogel, became available (Colab Laboratories, Chicago Heights, Illinois). This product is not prone to drying, and gives superior separations of liver cell proteins when compared with four other types of cellulose acetate.
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