Corticosterone EIA Kit

SKU:BHT11900003
Research Validated
Overview
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Sandwich enzyme immunoassay for quantitative corticosterone measurement in serum, plasma, urine, dried fecal extracts, and tissue culture media. Species-independent; the primary rodent stress hormone with 18.6 pg/ml sensitivity.
Assay Type Sandwich EIA
Sensitivity 18.6 pg/ml
Detection Range 78.125–10,000 pg/ml
Sample Compatibility Multi-Matrix
Species Reactivity Species Independent
Detection Method Colorimetric (TMB)
Throughput 39 samples in duplicate
Options selector
Catalog no. Size
SKT-205-96 96 well
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 96 well
  • Lead time: options listed in "Availability Content"; other statuses may take longer.
  • Storage: 4ºC and -20ºC.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No SKT-205
Alternative Names (11β)-11,21-dihydroxypregn-4-ene-3,20-dione
Assay Type
  • Sandwich EIA (Enzyme Immunoassay)
Detection Method
  • Colorimetric Assay
Product Type
  • Sandwich ELISA Kit
  • Sandwich EIA (Enzyme Immunoassay)
Sample Type(s) Serum, EDTA Plasma, Heparin Plasma, Urine, Tissue Culture Media, Dried Fecal Samples
Sensitivity 18.6 pg/ml
Shipping Blue Ice
Species Species Independent
Storage 4ºC and -20ºC
Target Corticosterone

Scientific Background

Corticosterone (C₂₁H₃₀O₄) is the dominant glucocorticoid in rodents, synthesized by the adrenal cortex under ACTH stimulation and widely used as the primary model compound for studying hypothalamic–pituitary–adrenal (HPA) axis regulation and stress physiology. Unlike cortisol in humans, corticosterone is the principal endogenous ligand for both mineralocorticoid receptors (MR, high affinity) and glucocorticoid receptors (GR, lower affinity) in the rodent brain.

Chronic elevation of corticosterone has been shown to impair spatial memory and hippocampal long-term potentiation, alter sleep architecture, suppress neurogenesis in the dentate gyrus, and accelerate accumulation of phosphorylated α-synuclein in hypothalamic dopaminergic neurons—findings that directly link chronic stress physiology to Parkinson's disease pathology.

Corticosterone measurement in fecal extracts enables minimally invasive, longitudinal HPA axis profiling in murine and avian research models, avoiding the confounding acute stress responses associated with blood collection. Its measurement is foundational in stress neurobiology, behavioral pharmacology, and corticosteroid-pathway drug development.

Product Description

StressXpress®

The Corticosterone EIA Kit (Cat. # SKT-205) from StressMarq Biosciences is a research-grade kit for quantitative Corticosterone measurement in Serum, EDTA Plasma, Heparin Plasma, Urine, Tissue Culture Media, Dried Fecal Samples. This kit employs a sandwich immunoassay principle with colorimetric TMB/spectrophotometric readout on a standard 96-well microplate reader.

Product Specifications

Analyte / Target Corticosterone
Assay Type Sandwich EIA (Enzyme Immunoassay)
Detection Method Colorimetric (microplate spectrophotometry)
Sensitivity 18.6 pg/ml
Detection Range 78.125–10,000 pg/ml
Compatible Matrices Serum, EDTA Plasma, Heparin Plasma, Urine, Tissue Culture Media, Dried Fecal Samples
Species Reactivity Species Independent
Throughput 39 samples in duplicate
Platform Microplate (96-well)
Catalog Number SKT-205
Storage 4ºC and -20ºC
Trademark StressXpress®

Assay Principle

This kit uses a competitive or sandwich enzyme immunoassay (EIA) format—a microplate-based immunoassay technique functionally equivalent to ELISA. Corticosterone in the sample competes with enzyme-labeled conjugate for a limited number of antibody binding sites. Bound conjugate is detected colorimetrically via TMB substrate; absorbance is inversely proportional to the Corticosterone concentration, interpolated from a calibration curve (range: 78.125–10,000 pg/ml).

The kit measures total Corticosterone and is fully validated for use in Serum, EDTA Plasma, Heparin Plasma, Urine, Tissue Culture Media, Dried Fecal Samples. The Steroid Solid Extraction Protocol (where provided) enables reliable extraction from complex matrices such as dried fecal samples.

Kit Components

Component # Description Quantity / Volume
SKC-205A Coated Clear 96-Well Plate 1 Each
SKC-205B Corticosterone Standard 125 µl
SKC-205C StressXpress® Corticosterone Antibody 3 ml
SKC-205D StressXpress® Corticosterone Conjugate 3 ml
SKC-205E Assay Buffer 28 ml
SKC-205F Dissociation Reagent 1 ml
SKC-205G Wash Buffer Concentrate 30 ml
SKC-205H TMB Substrate 11 ml
SKC-205I Stop Solution 5 ml
SKC-205J Plate Sealer 1 each

Quality Control & Validation

✓ Peer-Reviewed & Research Validated

Each lot is validated for sensitivity, intra-assay precision (CV <10%), and linearity of recovery. Products from the StressXpress® range cite published peer-reviewed literature for independent validation.

Safety & Regulatory

Research Use Only (RUO). Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.

ADR Classification: Non-hazardous. Shipping: cold-chain (blue ice). Harmonized Tariff Code: 3822.19.0030 (UNSPSC: 12352203). Country of Origin: Canada.

What sample types are compatible with the Corticosterone EIA Kit?

The kit is validated for use with the following sample matrices: Serum, EDTA Plasma, Heparin Plasma, Urine, Tissue Culture Media, Dried Fecal Samples. Dried fecal samples require a solid-phase extraction step using the Steroid Solid Extraction Protocol (provided separately). Samples should be processed and stored according to the included kit booklet to ensure assay accuracy.

What is the sensitivity of this assay?

The minimum detectable dose (sensitivity) of this Corticosterone EIA Kit is 18.6 pg/ml. The quantification range spans 78.125–10,000 pg/ml. Samples falling outside this range should be diluted (high) or concentrated (low) accordingly.

How long does the assay take from start to finish?

Total assay time is approximately 2–3 hours. Key incubation steps include: antibody/sample incubation (varies by step; total assay time approximately 2–3 hours), conjugate incubation, and TMB substrate development. Refer to the Kit Booklet for the precise protocol timeline.

What equipment is required to run this assay?

A standard 96-well microplate spectrophotometer (ELISA plate reader) capable of measuring absorbance at 450 nm is required. Additional equipment includes a microplate washer or multichannel pipette, pipettes, and a timer. All reagents are supplied within the kit.

Is this kit validated for non-human (animal) samples?

Yes. This kit is species-independent—the assay detects Corticosterone based on structural recognition rather than species-specific antibodies. It is validated for use in human, murine, avian, and other mammalian matrices including dried fecal extracts commonly used in non-invasive stress biology studies.

What is the precision of this assay?

Intra-assay precision (within-run CV) is <10% across tested concentration ranges. Three or more samples of known concentration are tested in ≥20 replicates per lot to establish lot-specific precision certificates. Refer to the Kit Booklet for lot-specific CV data.

This product may be available in custom quantities, alternative formulations, or with additional quality certifications to meet specific experimental requirements. Contact our scientific team through the BioHippo product page to discuss custom sizing, bulk ordering, and specialized packaging options. Special pricing may be available for volume orders and institutional customers.

1. Hupé, J. M., James, A. C., Payne, B. R., Lomber, S. G., Girard, P., & Bullier, J. (1998). Cortical feedback improves discrimination between figure and background by V1, V2, and V3 neurons. Nature, 394(6695), 784–787. DOI: 10.1038/29555 2. Kitaysky, A. S., Kitaiskaia, E. V., Wingfield, J. C., & Piatt, J. F. (2001). Dietary restrictions cause chronic elevation of corticosterone and enhance stress response in red-legged kittiwake chicks. Journal of Comparative Physiology B, 171(8), 701–709. DOI: 10.1007/s003600100230 3. Thellin, O., Noel, G., Khuana, S., Ogle, C. K., & Horseman, N. D. (2001). Stress hormone secretion and gut signal transducer (STAT) proteins after burn injury in rats. Shock, 16(5), 393–397. DOI: 10.1097/00024382-200116050-00001 4. Kramer, K. M., & Sothern, R. B. (2001). Circadian characteristics of corticosterone secretion in red-backed voles (Clethrionomys gapperi). Chronobiology International, 18(6), 933–945. DOI: 10.1081/CBI-100107542 5. Vazquez-Palacios, G., Retana-Márquez, S., Bonilla-Jaime, H., & Velázquez-Moctezuma, J. (2001). Further definition of the effect of corticosterone on the sleep-wake pattern in the male rat. Pharmacology, Biochemistry, and Behavior, 70(2–3), 305–310. DOI: 10.1016/S0091-3057(01)00629-8 6. Bimpos, N. M., Xie, Y., Gomez-Isla, T., Domenger, D., & Hyman, B. T. (2024). Alpha-synuclein-induced stress sensitivity renders the Parkinson’s disease brain susceptible to neurodegeneration. Acta Neuropathologica Communications, 12, 100. DOI: 10.1186/s40478-024-01797-w. 7. Burtscher, J., Copin, J. C., Rodrigues, J., & Pernet, N. (2019). Chronic corticosterone aggravates behavioral and neuronal symptomatology in a mouse model of alpha-synuclein pathology. Neurobiology of Aging, 83, 11–20. DOI: 10.1016/j.neurobiolaging.2019.08.011
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