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Journal of Lipid Research, Vol 19, 578-584, Copyright © 1978 by Lipid Research, Inc.
NA Le, JS Melish, BC Roach, HN Ginsberg and WV Brown
A method for determining apoprotein B specific activity in radioiodinated
lipoproteins is described and validated. It utilizes organic solvents and
tetramethylurea in the isolation of apoprotein B from other radiolabeled
contaminants, both lipid and protein, in exogenously labeled VLDL. The
contaminants are also removed from those lipoprotein classes subsequently
derived from VLDL, namely IDL and LDL. The procedure requires approximately
50 microgram of apoB per analysis, allowing specific activity
determinations in triplicate on 3-ml plasma samples with a standard error
of less than 6%. Finally, data from a study of apoprotein B turnover in
VLDL, IDL, and LDL in a human subject is presented to demonstrate the
potential of this method in further elucidating the kinetic
interrelationships between these lipoprotein classes.
ARTICLES
Direct measurement of apoprotein B specific activity in 125I-labeled lipoproteins
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