Cortisol EIA Kit

SKU:BHT11900002
Research Validated
Overview
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Competitive enzyme immunoassay for quantitative cortisol measurement across multiple biological matrices. Species-independent; validated in serum, plasma, urine, saliva, dried fecal extracts, and tissue culture media. Sensitivity 17.3 pg/ml.
Assay Type Competitive EIA
Sensitivity 17.3 pg/ml
Detection Range 100–3,200 pg/ml
Sample Compatibility Multi-Matrix
Species Reactivity Species Independent
Detection Method Colorimetric (TMB)
Throughput 40 samples in duplicate
Options selector
Catalog no. Size
SKT-201-96 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.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: refrigerate upon receipt.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No SKT-201
Alternative Names (11β)-11,17,21-trihydroxypregn-4-ene-3,20-dione
Assay Type
  • Competitive EIA (Enzyme Immunoassay)
Detection Method
  • Colorimetric Assay
Product Type
  • Competitive ELISA Kit
  • Competitive EIA (Enzyme Immunoassay)
Sample Type(s) Dried Fecal Samples, Saliva, Urine, Serum, EDTA Plasma, Heparin Plasma, Tissue Culture Media
Sensitivity 17.3 pg/ml
Shipping Blue Ice
Species Species Independent
Storage 4ºC
Target Cortisol

Scientific Background

Cortisol (C₂₁H₃₀O₅), the primary glucocorticoid hormone produced by the zona fasciculata of the adrenal cortex, is synthesized in an ACTH-dependent manner following activation of the hypothalamic–pituitary–adrenal (HPA) axis. Its secretion follows a robust diurnal rhythm, peaking in the early morning (06:00–08:00) and declining to nadir in late evening—a pattern disrupted in depression, Cushing's syndrome, and post-traumatic stress disorder.

Only free cortisol (~4% of total circulating cortisol) is biologically active and able to traverse the blood–brain barrier to bind glucocorticoid receptors (GR) widely expressed in the hippocampus, prefrontal cortex, and amygdala. Chronic HPA axis dysregulation suppresses hippocampal neurogenesis, reduces BDNF expression, and promotes dendritic atrophy in pyramidal neurons—mechanisms implicated in stress-induced depression, MCI, and accelerated neurodegeneration in Alzheimer's disease.

Cortisol measurement in multiple biological matrices (serum, saliva, urine, fecal extracts) allows non-invasive longitudinal profiling of HPA axis reactivity, making it an indispensable biomarker in stress biology, psychoneuroimmunology, and clinical neuroscience research.

Product Description

StressXpress®

The Cortisol EIA Kit (Cat. # SKT-201) from StressMarq Biosciences is a research-grade kit for quantitative Cortisol measurement in Dried Fecal Samples, Saliva, Urine, Serum, EDTA Plasma, Heparin Plasma, Tissue Culture Media. This kit employs a competitive immunoassay principle with colorimetric TMB/spectrophotometric readout on a standard 96-well microplate reader.

Product Specifications

Analyte / Target Cortisol
Assay Type Competitive EIA (Enzyme Immunoassay)
Detection Method Colorimetric (microplate spectrophotometry)
Sensitivity 17.3 pg/ml
Detection Range 100–3,200 pg/ml
Compatible Matrices Dried Fecal Samples, Saliva, Urine, Serum, EDTA Plasma, Heparin Plasma, Tissue Culture Media
Species Reactivity Species Independent
Throughput 40 samples in duplicate
Incubation Time 90 Minutes
Platform Microplate (96-well)
Catalog Number SKT-201
Storage 4ºC
Trademark StressXpress®

Assay Principle

This kit uses a competitive or sandwich enzyme immunoassay (EIA) format—a microplate-based immunoassay technique functionally equivalent to ELISA. Cortisol 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 Cortisol concentration, interpolated from a calibration curve (range: 100–3,200 pg/ml).

The kit measures total Cortisol and is fully validated for use in Dried Fecal Samples, Saliva, Urine, Serum, EDTA Plasma, Heparin Plasma, Tissue Culture Media. 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-201A Clear Microtitre 96-well Plate 1 Plate
SKC-201B Cortisol Standard 125 µl
SKC-201C StressXpress® Cortisol Antibody 3 ml
SKC-201D StressXpress® Cortisol Conjugate 3 ml
SKC-201E Assay Buffer 28 ml
SKC-201F Dissociation Reagent 1 ml
SKC-201G Wash Buffer Concentrate 30 ml
SKC-201H TMB Substrate 11 ml
SKC-201I Stop Solution 5 ml
SKC-201J 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 Cortisol EIA Kit?

The kit is validated for use with the following sample matrices: Dried Fecal Samples, Saliva, Urine, Serum, EDTA Plasma, Heparin Plasma, Tissue Culture Media. 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 Cortisol EIA Kit is 17.3 pg/ml. The quantification range spans 100–3,200 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 (90 Minutes), 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 Cortisol 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. E. Friess, et al., Eur J Clin Invest, 2000, 30, Suppl 3:46-50. 2. Freeman, Scott, 2002. Biological Science. Prentice Hall; 2nd Pkg edition (December 30, 2004). 3. C. Longscope., J. Endocrinology, 1996, , Suppl S125-S127. 4. J. Herbert, Lancet, 1995 345, 1193-1194. 5. A. Michael, et al., Biol. Psychiatry, 2000, 48, 989-95. 6. C.R. Dequet and D.J. Wallace, Current Opin. Ivest. Drugs, 2001, 8, 1045-53. 7. W.M. Jeffries, Med. Hypotheses, 1998, 51, 114-4.
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