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In Vitro Diagnostics

Immunoassay
体外診断用医薬品のイメージ画像

17-OH Progesterone ELISA “DP”

JANcode
4987797402018
Approval/Certification Number
30200EZX00086000
Insurance Points
213
Reference Value
Reference range
0.082~2.285 ng/mL
Measurement Time
5hours

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PRODUCT FEATURES

Introduction

This product is an in vitro diagnostic reagent intended for measuring serum 17α-Hydroxyprogesterone (17-OHP) by ELISA (Enzyme-Linked Immunosorbent Assay).

17α-Hydroxyprogesterone is markedly elevated in 21-hydroxylase deficiency, which accounts for approximately 95% of cases of congenital adrenal hyperplasia, due to deficiency of the 21-hydroxylase enzyme. Measurement of serum E is considered useful as an adjunctive aid in the early diagnosis of 21-hydroxylase deficiency and as an indicator for treatment monitoring.

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