Progesterone Radioimmunoassay
- Regulatory Status
- EU: CE
- Kit size
- 96
- Method
- RIA (CT)
- Incubation time
- 1 x 2h (37°C)
- Standard range
- 0.12 - 36 ng/mL
- Specimen / Volumes
- 50 µL Serum
- Substrate / isotope
- 125I < 220 kBq
Progesterone is a C-21 steroid hormone (molecular weight: 314.5) which is synthesized from cholesterol via pregnenolone in the granulosa and theca cells of the corpus luteum under the influence of LH. The major production sites are ovary and placenta and somewhat the adrenal cortex in both men and women. Progesterone is rapidly metabolized in the liver. Blood levels are very low during the follicular phase whereas one does observe a sharply increase during the luteal phase of menstrual cycles reaching a maximum some 5 to 10 days after the midcycle LH peak.
Serum progesterone levels, which are low during the follicular phase, increase during the luteal phase of menstrual cycle. Unless pregnancy occurs, the progesterone level declines 4 days before the next menstrual period. Thus, the measurement of progesterone levels constitutes a well-established method for detection of ovulation. But there are many cases where the progesterone measurements are also of interest:
For concrete data please consult the Instruction for Use in the download box on the top right side.
Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.
And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.
All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use.
All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).

As part of the Tecan Group, we have a leading market position in diagnostics and research, with over 40 years of experience in the development, manufacture and supply of enzyme-, radiolabel- and luminescence-based immunoassays.
Our range of high-quality immunoassays is supported by a diverse portfolio of automated solutions, making us the perfect partner for you and your customers.
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