Bovine IFN gamma ELISA

Catalog Number:
DIY0665B
Availability:
In stock
Application:
ELISA
100% Homology:
Bos frontalis (gayal), Bos taurus (cattle)

Components

UsageQuantityComponentSize
Detection Antibody50 µgPBB0267B-050
Standard5 µgRP0013B-005
Capture Antibody100 µgPB0156B-1001 Pack (<= 10 Plates)
Capture Antibody100 µg X 2PB0156B-1001 Pack (<= 20 Plates)
  • The Bovine IFN-γ (Interferon Gamma) ELISA is designed for the quantitative measurement of bovine interferon gamma 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, including serum, plasma, whole blood-derived culture supernatants, peripheral blood mononuclear cell (PBMC) culture supernatants, tissue homogenates or lysates, bronchoalveolar lavage fluid (BALF), and milk, depending on the experimental model and disease context. This flexibility supports a wide range of immunology and translational research applications. Interferon gamma (IFN-γ) is a central immunoregulatory cytokine and the signature cytokine of Th1-type immune responses. It plays a critical role in macrophage activation, antigen presentation, and cell-mediated immunity, and is produced primarily by T cells and natural killer (NK) cells in response to infection or immune stimulation. Measurement of IFN-γ is widely used to assess cell-mediated immune function, inflammatory responses, and host defense mechanisms during infectious disease, vaccine response, autoimmune conditions, and chronic inflammatory disorders. In bovine and related species, IFN-γ is a key biomarker of protective immunity and disease progression, supporting research in animal health, infectious disease, and comparative immunology. The bovine IFN-γ protein is 100% homologous to Gayal (Bos frontalis) IFN-γ, making this ELISA well suited for studies involving Gayal and closely related species where sequence identity supports cross-species detection. 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
Bovine Interferon-Gamma (IFN-γ) is a type II interferon produced primarily by activated CD4⁺ and CD8⁺ T lymphocytes and natural killer (NK) cells in cattle (Bos taurus), where it plays a central role in cell-mediated (Th1-type) immunity against intracellular pathogens. IFN-γ signals through the IFN-γ receptor complex (IFNGR1/IFNGR2), activating JAK/STAT1 pathways and inducing genes involved in macrophage activation, enhanced antigen presentation via upregulation of MHC class I and II molecules, nitric oxide production, and promotion of cytotoxic T-cell responses. In bovine health, IFN-γ is critically important for defense against economically significant intracellular infections such as Mycobacterium bovis (bovine tuberculosis), Mycobacterium avium subsp. paratuberculosis (Johne’s disease), Brucella abortus, and certain viral pathogens including bovine viral diarrhea virus (BVDV). Measurement of antigen-specific IFN-γ release forms the basis of widely used diagnostic assays for bovine tuberculosis and serves as an indicator of cellular immune activation and vaccine responsiveness. Dysregulated or insufficient IFN-γ responses can contribute to chronic infection, pathogen persistence, and altered disease progression. In veterinary and translational research, characterization of bovine IFN-γ supports studies of host–pathogen interactions, Th1/Th2 immune balance, vaccine efficacy, and immune correlates of protection, while also providing a valuable large-animal model for understanding cell-mediated immunity relevant to human tuberculosis and other intracellular infectious diseases.

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