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).
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:
TRIVITRON HEALTHCARE PVT. LTD.
рд╕рд░реНрд╡рд╛рдзрд┐рдХрд╛рд░ рд╕реБрд░рдХреНрд╖рд┐рдд.(рдЙрдкрдпреЛрдЧ рдХреА рд╢рд░реНрддреЗрдВ) рдЗрдиреНрдлреЛрдХреЙрдо рдиреЗрдЯрд╡рд░реНрдХ рдкреНрд░рд╛рдЗрд╡реЗрдЯ рд▓рд┐рдорд┐рдЯреЗрдб . рджреНрд╡рд╛рд░рд╛ рд╡рд┐рдХрд╕рд┐рдд рдПрд╡рдВ рдкреНрд░рдмрдВрдзрд┐рдд |