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Neonatal 17OH Progesterone FEIA


It is a competitive Fluorometric enzyme immunoassay for the quantitative determination of human 17-OH-progesterone from dried blood spots. It measures the 21-hydroxylase deficiency which is by far the most frequent form of CAH (more than 90 % of cases).

Labsystems Diagnostics’ Neonatal 17-OH-Progesterone FEIA test is a fluorometric enzyme immunoassay enabling the quantification of 17-hydroxyprogestrone steroid present in blood samples dried on filter paper. The test can be used for the screening of newborn for Congenital Adrenal Hyperplasia (CAH).
Benefits
Excellent reproducibility
High sensitivity with high signal/background ratio
Calibrated against the latest international references

Neonatal 17-OH-Progesterone FEIA , 5 strip plates (12×8), 480 wells 6199870
Neonatal 17-OH-Progesterone FEIA, 10 strip plate (12×8), 960 wells 6199872
Neonatal 17-OH-Progesterone FEIA, 10 solid plates (96), 960 wells 6199871

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