Equine IFN gamma ELISA

Catalog Number:
DIY0697E
Availability:
In stock
Application:
ELISA
100% Homology:
Equus caballus (horse)

Components

UsageQuantityComponentSize
Detection Antibody50 µgPBB0282E-050
Standard5 µgRP0012E-005
Capture Antibody500 µgMA0460E-5001 Pack (<= 10 Plates)
Capture Antibody500 µg X 2MA0460E-5001 Pack (<= 20 Plates)
  • The Equine IFN-γ (Interferon Gamma) ELISA is designed for the quantitative measurement of equine IFN-γ in cell culture supernatants. With minor modifications to the assay procedure, this ELISA may also be used to measure IFN-γ in additional biological sample types reported in the literature, including serum, plasma, peripheral blood mononuclear cell (PBMC) culture supernatants, and tissue homogenates or lysates, depending on the experimental model and physiological context. This flexibility supports a wide range of immunology and translational research applications. Reported measurements: Equine IFN-γ has been detected in serum (~50-900 pg/mL), plasma (~40-800 pg/mL), and PBMC culture supernatants (~100-2000 pg/mL under stimulation conditions), although levels vary depending on immune activation, infection, or experimental treatment. Interferon Gamma (IFN-γ) is a cytokine primarily produced by activated T lymphocytes and natural killer (NK) cells. It plays a central role in cell-mediated immunity, macrophage activation, antiviral defense, and regulation of Th1 responses. Measurement of IFN-γ is widely used to assess immune activation, vaccine efficacy, infection response, and inflammatory signaling in horses and related species. IFN-γ serves as an important biomarker of adaptive immune function, pathogen response, and overall immune system activity, supporting studies in equine immunology, comparative immunology, and translational research. Why measure Equine IFN-γ: Measuring IFN-γ provides critical insight into Th1-driven immune responses, cell-mediated immunity, and host defense mechanisms. Quantifying IFN-γ helps evaluate vaccine responses, infection-induced immune activation, and immunomodulatory treatments, making it a key biomarker for both basic and applied research in equine immunology. IFN-γ is a member of the type II interferon family, which contributes to antiviral defense, immune regulation, and inflammation, specifically orchestrating adaptive cell-mediated immunity. The kit contains a capture antibody, detection antibody, and recombinant protein standard for assay development. These antibodies have been validated to function together in an ELISA format using the provided standard. Optimal buffers, antibody concentrations, incubation times, temperatures, and assay conditions have not been predetermined, allowing researchers to optimize assay sensitivity and dynamic range based on their specific sample type and experimental requirements. The quantities of kit components are not matched, and individual components may be purchased separately. This product is for research use only and is manufactured in the USA.
Storage Conditions2°C to 8°C or -20°C
Country Of OriginUSA
Equine Interferon-γ (IFN-γ) is a type II interferon cytokine that plays a central role in cell-mediated immunity and regulation of antimicrobial responses in horses (Equus caballus). IFN-γ is primarily produced by activated T helper 1 (Th1) lymphocytes, cytotoxic T cells, and natural killer (NK) cells following stimulation by intracellular pathogens or inflammatory cytokines. Equine IFN-γ binds to the interferon-γ receptor (IFNGR) expressed on many immune and non-immune cells, activating intracellular signaling through the JAK–STAT pathway, particularly STAT1, which induces transcription of interferon-stimulated genes involved in antimicrobial defense, antigen presentation, and immune regulation. In horses, IFN-γ is critical for macrophage activation, enhanced antigen presentation via MHC molecules, and control of intracellular pathogens. In equine health, IFN-γ contributes to immune responses against infectious diseases such as equine herpesvirus and Rhodococcus equi infections. Horses are also used as animal models for respiratory and intracellular bacterial infections, and IFN-γ–mediated immune responses have been studied in foal models of Rhodococcus equi pneumonia, where IFN-γ–driven macrophage activation is important for controlling intracellular bacterial replication, providing insights relevant to both equine infectious disease and comparative studies of pulmonary immunity.

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