Equine CCL4 (MIP-1 beta) ELISA

Catalog Number:
DIY1221E
Availability:
In stock
Application:
ELISA
100% Homology:
Equus caballus (horse), Equus przewalskii (Przewalski's horse)

Components

UsageQuantityComponentSize
Detection Antibody50 µgPBB0330S-050
Standard5 µgRP0981E-005
Capture Antibody100 µgPB0329S-1001 Pack (<= 10 Plates)
Capture Antibody100 µg X 2PB0329S-1001 Pack (<= 20 Plates)
  • The Equine CCL4 (C-C motif chemokine ligand 4, also known as MIP-1β) ELISA is designed for the quantitative measurement of CCL4 in cell culture supernatants from horses and can also be used to measure CCL4 in a wide variety of biological sample types reported in the literature, including serum, plasma, whole blood, and tissue lysates from organs such as spleen, lung, liver, and lymph nodes. While the kit is optimized for cell culture supernatants, minor modifications to the protocol may be required when measuring CCL4 in other sample types to ensure optimal sensitivity and accuracy, allowing researchers to adjust buffers, antibody concentrations, incubation times, temperatures, and other assay conditions as needed. CCL4 is a chemokine primarily produced by monocytes, macrophages, T lymphocytes, and dendritic cells and plays a central role in recruiting immune cells, including T cells, natural killer (NK) cells, and monocytes, to sites of inflammation or infection. In the equine animal model, CCL4 is widely studied in the context of infectious disease, inflammatory disorders, and immune regulation, where its expression reflects immune activation and chemokine signaling. Measurement of equine CCL4 provides valuable insight into immune response dynamics, inflammation, disease progression, and the efficacy of immunomodulatory or therapeutic interventions, with reported levels in horses typically detected at low picogram-per-milliliter concentrations under basal conditions (~50-200 pg/mL in serum or plasma) and increasing to hundreds to over a thousand picograms per milliliter during immune stimulation or inflammatory challenge, depending on sample type and experimental context. The kit contains a capture antibody, detection antibody, and recombinant equine CCL4 protein standard for assay development, and these antibodies have been validated to function together in an ELISA format using the provided standard. 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 CCL4 (C-C motif chemokine ligand 4, also known as MIP-1β, macrophage inflammatory protein-1 beta) is a pro-inflammatory chemokine that regulates recruitment and activation of immune cells during inflammatory and infectious responses in horses (Equus caballus). CCL4 primarily signals through the CCR5 receptor, promoting chemotaxis of monocytes, macrophages, dendritic cells, natural killer (NK) cells, and activated T lymphocytes to sites of infection or tissue injury. In horses, CCL4 is produced by activated macrophages, dendritic cells, epithelial cells, and lymphocytes in response to inflammatory stimuli such as microbial components and cytokines including TNF-α and IL-1β. CCL4-mediated immune cell recruitment contributes to host defense in diseases such as equine influenza virus infection, bacterial pneumonia, and other respiratory pathogens, where leukocyte trafficking to lung tissue helps coordinate antiviral and antibacterial immune responses. It may also play roles in musculoskeletal inflammation and joint disease, where infiltration of immune cells contributes to inflammatory signaling and tissue remodeling. While CCL4-driven leukocyte migration supports pathogen clearance and immune activation, excessive or prolonged expression may contribute to inflammatory tissue damage. As a regulator of immune cell trafficking and inflammatory signaling, equine CCL4 is important in studies of host–pathogen interactions, respiratory disease, and inflammatory mechanisms affecting equine health and performance.

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