Key result
Simplified acrylamide gel disc electrophoresis sharply resolves human serum lipoproteins into alpha, beta, and pre-beta bands.
Why the study?
A simplified and integrated method for human serum lipoprotein disc electrophoresis was needed based on previous investigations of lipoprotein behavior in acrylamide gel systems.
Simplifies serum lipoprotein separation in research settings; leaves open any role in routine clinical lipid assessment.
An integrated and simplified method for acrylamide gel Disc electrophoresis was devised in this study based on results obtained by the previous study where general behavior of human serum lipoproteins in various acrylamide gel systems was investigated. Acrylamide gel concentrations employed in this method were 3.75% for separating gel, 2.5% for spacer gel and 3.3% for sample gel. For lipoprotein staining, serum samples were mixed with a sample gel solution in which Sudan Black B in ethylene glycol and buffered acrylamide solution with a combined catalyzer (TEMED-riboflavin) were included. Identification of lipoprotein bands on acrylamide gel columns was made by means of a combination of paper electrophoretic, acrylamide gel Disc electrophoretic and immunological techniques. It was established that human serum lipoproteins were sharply resolved and were arranged in the order of alpha, beta, and pre-beta lipoproteins from the anodal to cathodal end of the column. This method could be useful in clinical laboratories as well as in research laboratories for identification of human serum lipoprotein abnor-malities.
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Wada et al. (1972) studied Human serum lipoprotein abnormalities. Acrylamide gel Disc electrophoresis was evaluated on Resolution and identification of human serum lipoproteins. An integrated and simplified acrylamide gel disc electrophoresis method successfully and sharply resolved human serum lipoproteins into alpha, beta, and pre-beta bands.
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