Progesterone radioimmunoassay kit RIA
Overview
Ascertain whether ovulation occurred in a menstrual cycle
Evaluate patients with sterility due to suspected luteal phase defects
Benefits
- LOW ANALYTICAL DETECTION LIMIT
Assay principle: competition
Features
Working range: 0.05 – 36 ng/mL [Progesterone in nmol/L = 3.18 X Progesterone in ng/mL]
Sample: serum – 50 µL
Analytical sensitivity: 0.05 ng/mL
Normal values
Concentration range (ng/mL) | Number of subjects | |
---|---|---|
Males | 0.60 - 2.11 | 50 |
Females | ||
- Follicular phase | 0.70 - 1.78 | 34 |
- Ovulatory phase | 0.79 - 3.95 | 29 |
- Luteal phase | 4.57 - 17.56 | 39 |
- Menopause | 0.43 - 2.13 | 50 |
Immunoassays RIA and ELISA - Catalog
Immuno-analyse RIA et ELISA - Catalog
Annual availability Schedule 2021
In-vitro RIA products - Availability calendar
Calendrier de mise a disposition 2021
Trousse pour radioimmunologie - Availability calendar
Safety Data Sheet (ENG-GB) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (DEU) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (ELL) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (FRA-FR) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (ITA) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (SPA) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (ENG-GB) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Safety Data Sheet (ENG-US) PROG / PROGEST-RIA
PROGEST-RIA - Safety Data Sheet
Quality Control Report PROG / PROGEST-RIA
PROGEST-RIA Batch 210902 - Quality Control Report