17-OH-Progesterone ELISA
- Regulatory Status
- IVD
- Kit size
- 96
- Method
- ELISA
- Incubation time
- 1 x 60 min, 1 x 30 min
- Standard range
- 0.15 - 20 ng/mL
- Specimen / Volumes
- 25 µL serum, EDTA plasma
- Substrate / isotope
- TMB 450 nm
17-OHP is a steroid hormone, which can be found in circulation in the human body. The relevance of serum and several types of plasma for the quantification of steroidal hormones is well established in clinical diagnostics.1 Steroid profiling – including the quantification of 17-OHP – is routinely performed in different matrices such as serum and plasma, which is reflected in the composition of the different reference ranges found in the literature. The role of 17-OHP as an intermediate in the biosynthesis of cortisol is well established in the peer reviewed scientific literature.2
This enzyme immunoassay is intended for the quantitative determination of 17-hydroxyprogesterone (17-OHP) in human EDTA plasma and serum. Measurements of 17-hydroxyprogesterone are used in the diagnosis and treatment of various disorders of the adrenal glands or the ovaries. The 17-OH-Progesterone ELISA is NOT intended for use in neonatal screening, nor for diagnosis of genetic disorders, and not for use in monitoring patients with hypogonadotropic hypogonadism.
For concrete data please consult the Instruction for Use in the download box on the top right side.
1. Holst, J. P. et Al.; Steroid Hormones: Relevance and Measurement in the Clinical Laboratory. Clinics in Laboratory Medicine. NIH Public Access March 2004, pp 105–118 https://doi.org/10.1016/j.cll.2004.01.004.
2. Honour, J. W. 17-Hydroxyprogesterone in Children, Adolescents and Adults. Annals of Clinical Biochemistry. SAGE Publications Ltd July 7, 2014, pp 424–440. https://doi.org/10.1177/0004563214529748.
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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.
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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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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.
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