1979
DOI: 10.1016/0009-8981(79)90184-0
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The quantitation of pregnancy specific β1-glycoprotein by enzyme linked immunoassay

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Cited by 19 publications
(4 citation statements)
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“…The birthweights of the infants born to these control subjects were corrected for maternal height, weight and gestation according to the tables published by Thomson et al (1968) and each had a birthweight of 210th centile of weight for gestation. hPL concentrations were assayed by radioimmunoassay and SP, concentrations by an enzyme-linked immunosorbcnt assay (Macdonald et al 1979). hPL and SP, concentrations increased with advancing gestation to a peak between 36 and 38 weeks and the peak concentrations for hPL and SP, for each individual patient was used in this analysis.…”
Section: Methodsmentioning
confidence: 99%
“…The birthweights of the infants born to these control subjects were corrected for maternal height, weight and gestation according to the tables published by Thomson et al (1968) and each had a birthweight of 210th centile of weight for gestation. hPL concentrations were assayed by radioimmunoassay and SP, concentrations by an enzyme-linked immunosorbcnt assay (Macdonald et al 1979). hPL and SP, concentrations increased with advancing gestation to a peak between 36 and 38 weeks and the peak concentrations for hPL and SP, for each individual patient was used in this analysis.…”
Section: Methodsmentioning
confidence: 99%
“…The optimal conditions for the assay of cytosol and G2 binding with anti-MS antibodies were derived by the initial experimental set-up according to MacDon ald al. [3], The standard assay was as follows: 100 pi of the cytosol or G2 (1 pg protein/ml) was allowed to bind to the wells in micro ELISA plates (M 129A from Dynatech AG, Switzerland) at 4 °C for 18-20 h. The unbound material was aspirated and the wells were washed three times (1 min each) with 200 pi of 0.01 % Tween 20 in phosphate (0.1 M) buffer saline (0.14 M) pH 7.4. The remaining binding sites in the wells were saturated with 100 pi of I % (w/v) bovine serum albu min in phosphate buffer, I h at 22 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Pregnancy specific ß l glycoprotein is produced by the syncytiotrophoblasts during pregnancy, when peripheral blood concentrations greater than 400 mg/1 may occur during the last trimester (1). Additionally pregnancy Materials and Methods specific ft glycoprotein may be produced by trophoReagents blastic tumours in both men and women but under these ^ p re gnancy specific ß l glycoprotein standards -Hoechst Circumstances serum concentrations are 1/1000 of those Pharmaceuticals, Hounslow, England -A range of dilutions was • -" .…”
Section: Introductionmentioning
confidence: 99%
“…Supplied by Mercia Brocades. linked immunosorbent assay (1). Enzyme linked immuno-Diluted 1:1200 in carbonate-hydrogencarbonate buffer (pH 9.6) sorbent assay has several advantages over radioimmunobefore use · assay (4) so we wished to apply the technique to serum pregnancy specific ft glycoprotein analysis in malignancy.…”
Section: Introductionmentioning
confidence: 99%