A specific radioimmunoassay for androstenedione with reduced bridge-binding |
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Authors: | G D Nordblom R E Counsell B G England |
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Affiliation: | 1. Department of Pathology, University of Michigan, Ann Arbor, MI 48109 USA;2. Department of Pharmacology, University of Michigan, Ann Arbor, MI 48109 USA |
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Abstract: | Antibody used in a steroid radioimmunoassay raised against a steroid hapten-carrier protein conjugate may recognize both the hapten and the chemical bridge to the protein. Use of the same bridge in the radio-isotopic label may lead to higher affinity binding to the label than to the native steroid. Inhibition curves under these conditions are shallow and generally not acceptable for radioimmunoassay procedures. We have developed a radioimmunoassay for androstenedione that employs different bridges at the 11 beta position of the steroid for the protein conjugate and label. The resulting assay has greatly reduced bridge-binding, has an acceptable slope for the standard curve and is very specific as evidenced by low crossreactivies to other steroids. |
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Keywords: | Trivial steroid names used are androstenedione, 4-androstene-3, 17-dione 5α-androstanedione, 5α-androstane-3, 17-dione dehydroepiandrosterone, 3β-hydroxy-5-androsten-17-one androsterone, 3α-hydroxy-5α-androstan-17-one testosterone, 17β-hydroxy-4-androsten-3-one 11β-hydroxyandrostenedione, 11β-hydroxy-4-androstene-3, 17-dione 5α-dihydrotestosterone, 17β-hydroxy-5α-androstan-3-one progesterone, 4-pregnene-3, 20-dione estradiol-17β, 1, 3, 5, (10)-estratriene-3, 17β-diol The computer program we used defined the limit of detection as 100% binding less two standard deviations of the assay or 100% binding less two standard deviations of the buffer control whichever had the lower mean variance ratio |
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