1989
DOI: 10.1093/clinchem/35.7.1380
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Lipoprotein(a) quantified by an enzyme-linked immunosorbent assay with monoclonal antibodies.

Abstract: This new, sensitive, specific "sandwich"-type enzyme-linked immunosorbent assay (ELISA) for quantifying lipoprotein(a) [Lp(a)] in human serum and in ultracentrifugal lipoprotein fractions is based on use of a monoclonal antibody raised against apolipoprotein(a) as coating protein and a polyclonal antibody, raised against either apo B or against Lp(a) and conjugated with peroxidase, for detection of bound Lp(a). Mean intra- and interassay CVs for assay of 16 samples were 3.0% and 5.6%, respectively. Sample pret… Show more

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Cited by 64 publications
(8 citation statements)
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“…Lipoprotein A in cord blood is characterized by low concentrations, approximately 2.6‐fold lower than the concentration of LpA found in our previous study in children. The gradual increase of LpA concentration throughout the first year of life, observed in other studies 18 , 21 , 22 accounts for the interpretation that very low LpA values found at birth in the present study are a real phenomenon.…”
Section: Discussionsupporting
confidence: 85%
“…Lipoprotein A in cord blood is characterized by low concentrations, approximately 2.6‐fold lower than the concentration of LpA found in our previous study in children. The gradual increase of LpA concentration throughout the first year of life, observed in other studies 18 , 21 , 22 accounts for the interpretation that very low LpA values found at birth in the present study are a real phenomenon.…”
Section: Discussionsupporting
confidence: 85%
“…Plasma Lp(a) levels increase soon between a er birth until the 7th postnatal day [188] and reach a constant concentration within a few months of life [189]. In adults, Lp(a) levels range widely, from <2 up to 2500 mg/L [190].…”
Section: Screeningmentioning
confidence: 99%
“…A variety of methodological approaches have been used. Early methods included radial immunodiffusion, 11 radioimmunoassay 12 and electroimmunoassay, 13 but these were superseded by more sensitive, less labour-intensive enzymelinked immunosorbent assays (ELISAs) and immunoradiometric assays (IRMAs). 14,15 More recently, immunoturbidimetric and nephelometric methods have become more popular due to their rapid throughput, ease of automation and now improved precision.…”
Section: Kits For the Measurement Of Lp(a)mentioning
confidence: 99%