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Neonatal 17OH Progesterone FEIA

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).

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Overview
Technical Specifications
Benefits

Overview

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).

Technical Specifications

Neonatal 17-OH-Progesterone FEIA , 5 strip plates (12x8), 480 wells 6199870
Neonatal 17-OH-Progesterone FEIA, 10 strip plate (12x8), 960 wells 6199872
Neonatal 17-OH-Progesterone FEIA, 10 solid plates (96), 960 wells 6199871

Benefits

Excellent reproducibility
High sensitivity with high signal/background ratio
Calibrated against the latest international references

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