1980
DOI: 10.1093/clinchem/26.11.1607
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Radioimmunoassay of progesterone in unextracted serum.

Abstract: We describe a rapid, precise radiommunoassay for progesterone in 25 muL of unextracted serum. Progesterone is released from its binding protein by adding an optimal amount of cortisol, which binds to the same protein (cortisol binding globulin) as progesterone. The amount of cortisol required does not cross react with the specific progesterone antibody used. This approach considerably shortens assay time and removes a tedious and imprecise stage in the conventional assay of serum progesterone. Results correlat… Show more

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Cited by 24 publications
(3 citation statements)
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“…A standard ICP-OES (Perkin-Elmer, Optima 2000 DV®) analyzer system was used for the determination according to (Oser 1965). Progesterone was estimated in both plasma and milk by the radioimmunoassay (RIA) technique using the coated tube kits according to Haynes et al (1980) and Blight & White (1983). The kit was purchased from Institute of Isotopes Co. LTD. Budapest and was labelled with I 125.…”
Section: Methodsmentioning
confidence: 99%
“…A standard ICP-OES (Perkin-Elmer, Optima 2000 DV®) analyzer system was used for the determination according to (Oser 1965). Progesterone was estimated in both plasma and milk by the radioimmunoassay (RIA) technique using the coated tube kits according to Haynes et al (1980) and Blight & White (1983). The kit was purchased from Institute of Isotopes Co. LTD. Budapest and was labelled with I 125.…”
Section: Methodsmentioning
confidence: 99%
“…Serum progesterone was estimated by Radioimmunoassay (RIA) using Coat -A count 1 125 progesterone kit (Diagnostic product corporation, Los Angeles, USA) according to Haynes et al (1980) and Kubasik et al (1984). The quantitative measurement of Estradiol in serum was done by RIA using coat-A count 1 125 Estradiol 17-β kit (Diagnostic product corporation, Los Angeles, USA) according to Xing et al (1983).…”
Section: Blood Samplesmentioning
confidence: 99%
“…Commercial ELISA relies on the use of progesterone-enzyme conjugates and these lack an efficient and convenient purification method (Mitchell et al 2004). Conventional assays involve extraction of progesterone from serum by organic solvent; however, the direct assay of progesterone in unextracted serum has also been described (Haynes et al 1980, Ratcliffe 1982, Lagana et al 1986).…”
Section: Introductionmentioning
confidence: 99%