1970
DOI: 10.1530/acta.0.065s305
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ASSAY OF 17β-Oestradiol BY COMPETITIVE PROTEIN BINDING METHODS

Abstract: This report gives details of the authors' procedure for the measurement of 17β-oestradiol in plasma by competitive protein binding analysis, together with the results of studies on various parameters of the assay system. The preparation of the receptor cytosol, the assay system, extraction of plasma and reliability criteria are all discussed. The procedure is compared with those reported by other workers. Finally the results obtained by this technique are compared with those obtained by other methods and curre… Show more

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Cited by 20 publications
(4 citation statements)
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“…The antiserum used was relatively specific for oestradiol with only a 5% cross-reaction with oestrone. Levels of immunoreactive oestrogens by this method corresponded closely with those obtained using a competitive protein-binding method specific for oestradiol (Corker, Exley, and Naftolin, 1970). The average coefficient of variance of oestradiol recovery from a pooled plasma sample was 6%.…”
Section: Methods Of Assay Plasma Luteinizing Hormone (Lh) This Wassupporting
confidence: 68%
“…The antiserum used was relatively specific for oestradiol with only a 5% cross-reaction with oestrone. Levels of immunoreactive oestrogens by this method corresponded closely with those obtained using a competitive protein-binding method specific for oestradiol (Corker, Exley, and Naftolin, 1970). The average coefficient of variance of oestradiol recovery from a pooled plasma sample was 6%.…”
Section: Methods Of Assay Plasma Luteinizing Hormone (Lh) This Wassupporting
confidence: 68%
“…These eluates were divided into three equal portions; one of these served for determining the recovery of the radioactive internal standard, and the other two for the CPB assay. The assay was done in duplicate according to the method of Korenman (1968), as modified by Corker, Exley «fe Naftolin (1970).…”
Section: Animals and Blood Collectionsmentioning
confidence: 99%
“…After incubation with 20 nM-[3H]DHT for 20 h, the nuclear extracts were precipitated with protamine sulphate and filtered on Whatman GF/C filters. The filters were then extracted three times with méthylène dichloride and the extracted steroids were chromatographed on thin-layer alumina gel plates using benzene-ethanol (20/1, v/v) (Corker, Exley & Naftolin, 1970). At the end of incubation, Chromato¬ graphie analysis indicated that 74% of the [3H]DHT was unchanged.…”
Section: Methodsmentioning
confidence: 99%