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Journal of Lipid Research, Vol 22, 514-518, Copyright © 1981 by Lipid Research, Inc.
CE Sparks and JB Marsh
Rat plasma, containing 125I-labeled triglyceride-rich lipoprotein, was
mixed following lipid extraction with 10% SDS buffer and analyzed by gel
filtration chromatography on columns using an elution buffer containing 1%
SDS. Labeled apoproteins were separated into apo B, apo E, and apo C
radioactivity peaks. Labeled peptides, tyrosine, and iodide were also
resolved by this method. Isolated lipoprotein fractions were separated into
the same components. The method offers the advantages of quantitative
radioactivity recovery, large sample volume, and resolution of two apo B
proteins.
ARTICLES
Analysis of lipoprotein apoproteins by SDS-gel filtration column chromatography
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