
pmid: 4205489
ABSTRACT A method of haemagglutination inhibition assay of HCS was developed utilizing formaldehyde and glutaraldehyde to conjugate the hormone to sheep red blood cells. This technique is sufficiently sensitive (8.7 ng/ml) so that assay of HCS from early pregnancy serum (17 weeks of gestation) can be performed directly after 1:50 dilution. Results can be obtained within 3 h. HCS sensitized red blood cells were shown to be stable for several months. HCS levels of 20 normal pregnancies were estimated throughout gestation. Forty-two sera from pregnant subjects were assayed by this technique and radioimmunoassay (RIA). The values obtained by the 2 methods had excellent correlation (r = 0.95). Reproducibility of the present method was ± 15 %. Data of HCS serum levels obtained by the present technique and by RIA in high-risk pregnancies are compared and the conclusion is reached that any of these techniques can be used for the successful clinical assay of HCS.
Erythrocytes, Sheep, Immune Sera, Infant, Newborn, Radioimmunoassay, Hemagglutination Inhibition Tests, Placental Lactogen, Chorionic Gonadotropin, Pregnancy Complications, Obstetric Labor, Premature, Pre-Eclampsia, Glutaral, Pregnancy, Formaldehyde, Methods, Animals, Humans, Cattle, Female, Rabbits
Erythrocytes, Sheep, Immune Sera, Infant, Newborn, Radioimmunoassay, Hemagglutination Inhibition Tests, Placental Lactogen, Chorionic Gonadotropin, Pregnancy Complications, Obstetric Labor, Premature, Pre-Eclampsia, Glutaral, Pregnancy, Formaldehyde, Methods, Animals, Humans, Cattle, Female, Rabbits
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