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Progesterone Radioimmunoassay

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Catalog no.MG12171
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
instructions for useMSDS

Radioimmunoassay for the in vitro quantitative measurement of human Progesterone in serum.

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.

Clinical applications

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:

  • To check the effectiveness of ovulation induction;
  • To monitor the embryo transfer and progesterone replacement therapy;
  • To detect the patients at risk for abortion during the beginning of pregnancy;
  • To aid in the diagnostic of ectopic pregnancy;
  • To detect all ovarian tumor (benign and malign) in postmenopausal women;
  • To diagnose luteinized unruptured follicle by the dosage of 17 beta-estradiol and progesterone levels in peritoneal fluid;
  • The steroid profiles of follicular fluids and the ratio of E2/PROG allow detecting a normal or adysfunctional ovulation induction. (The empty follicular syndrome may reflect a dysfunctional ovulation induction).

For concrete data please consult the Instruction for Use in the download box on the top right side.

Our Product Families

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).

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This is who we are.

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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At Tecan, we are driven to improve people’s lives and health.