Progesterone Radioimmunoassay
- Regulatory Status
- RUO
- 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
Immunoradiometric Assay (Coated Tube) for the quantitative determination of progesterone in human serum.
For research use only. Not for use in diagnostic procedures.
Test Principle
A fixed amount of 125I labelled steroid competes with the steroid to be measured present in the sample or in the calibrator for a fixed amount of antibody sites being immobilized to the wall of a polystyrene tube. Neither extraction nor chromatography is required. After 2 hours incubation at 37°C in a water bath, an aspiration step terminates the competition reaction. The tubes are then washed with 3 ml of wash solution and aspirated again. A calibration curve is plotted and the Progesterone concentrations of the samples are determined by dose interpolation from the calibration curve.
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.
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).
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.
Happy to help.
At Tecan, we are driven to improve people’s lives and health.