17 alpha-hydroxyprogesterone radioimmunoassay kit RIA
Overview
Diagnosis congenital hyperplasia of the adrenal glands early
Monitor treatment for congenital hyperplasia of the adrenal glands
Benefits
- LOW ANALYTICAL DETECTION LIMIT
Assay principle: competition
The principle of the assay is based on competition between the 17a-OHP radiolabeled with iodine-125 and the 17a-OHP to be assayed contained in the samples for a given number of antibody binding sites adsorbed onto the tube walls. NB: extraction step for pregnant women at the 3rd trimester and newborn children.
One-step assay procedure: 2h30 at 37°C.
Features
Working range: 0.09 – 75.7 nmol/L [0.10 – 25 ng/mL] (nmol 17 a-hydroxyprogesterone/L = ng/mL x 3.03)
Sample: serum, EDTA or heparin plasma – 25 µL
Analytical sensitivity: 0.09 nmol/L
Normal values
Population | 17 OHP ng/mL | 17OHP nmol/L |
---|---|---|
Reproductive aged women | ||
Follicular phase | 0.10 - 0.80 | 0.303 - 2.42 |
Luteal phase | 0.27 - 2.90 | 0.82 - 8.78 |
Post ACTH | <3.2 | <9.69 |
Normal men | 0.31 - 2.17 | 0.94 - 6.57 |
Third trimester pregnant women* | 2 - 12 | 6.06 - 36.36 |
Newborn* | <0.7 - 2.5 | 2.12 - 7.5 |
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Annual availability Schedule 2021
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Product Insert (ENG) OHP / OHP-CT
OHP-CT Op.Mod.020 - Product Insert
Product Insert (FRA) OHP / OHP-CT
OHP-CT Op.Mod.020 - Product Insert
Quality Control Report OHP / OHP-CT
OHP-CT Batch 17PK2013CI - Quality Control Report