Corticosterone ELISA
- Regulatory Status
- IVD
- Kit size
- 12 x 8
- Method
- ELISA
- Incubation time
- 1 x 60 / 1 x 15 min
- Standard range
- 0 - 240.0 nmol/L
- Specimen / Volumes
- 20 µl serum, plasma
- Substrate / isotope
- TMB 450 nm
| instructions for use |
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| instructions for use |
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Intended Use
The DRG Corticosterone ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of corticosterone in serum or plasma (lithium heparin or citrate plasma).
Summary and Explanation
Corticosterone is a glucocorticoid secreted by the cortex of the adrenal gland. Corticosterone is produced in response to the stimulation of the adrenal cortex by adrenocorticotropic hormone (ACTH) and is the precursor of aldosterone. Corticosterone is a major indicator of stress since stress increases the production of corticosteroids. Studies involving corticosterone and levels of stress include impairment of long term memory retrieval [1], chronic corticosterone elevation due to dietary restrictions [2] and in response to burn injuries [3]. In addition to stress levels, corticosterone is believed to play a decisive role in sleep-wake patterns [4,5].
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.
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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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