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Human IL-1 Beta ELISPOT Kit is a ELISPOT Kit for the sensitive detection of Human IL-1 Beta production in a single cell suspension.
Alternative names=Interleukin-1 beta, IL-1 beta, Catabolin, IL1B, IL1F2
Colorimetric
Suspension cells
Sandwich (qualitative)
Human
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application ELISPOT | Reactivity Reacts | Dilution info - | Notes - |
Potent proinflammatory cytokine. Initially discovered as the major endogenous pyrogen, induces prostaglandin synthesis, neutrophil influx and activation, T-cell activation and cytokine production, B-cell activation and antibody production, and fibroblast proliferation and collagen production. Promotes Th17 differentiation of T-cells. Synergizes with IL12/interleukin-12 to induce IFNG synthesis from T-helper 1 (Th1) cells (PubMed:10653850). Plays a role in angiogenesis by inducing VEGF production synergistically with TNF and IL6 (PubMed:12794819).
Human IL-1 Beta ELISPOT Kit is a ELISPOT Kit for the sensitive detection of Human IL-1 Beta production in a single cell suspension.
Alternative names=Interleukin-1 beta, IL-1 beta, Catabolin, IL1B, IL1F2
Colorimetric
Suspension cells
Sandwich (qualitative)
Human
Microplate
Blue Ice
+4°C
+4°C
+4°C
The ELISPOT assay is designed to enumerate cytokine producing cells in a single cell suspension. This method has the advantage of requiring a minimum of in-vitro manipulations allowing cytokine production analysis as close as possible to in-vivo conditions in a highly specific way. This technique is designed to determine the frequency of cytokine producing cells under a given stimulation, and the follow-up of such frequency during a treatment and/or a pathological state. Elispot assay constitutes an ideal tool in the TH1 / TH2 response, vaccine development, viral infection monitoring and treatment, cancerology, infectious diseases, autoimmune diseases and transplantation.
Abcam Elispot assay is based on sandwich immuno-enzyme technology. Cell secreted cytokines or soluble molecules are captured by coated antibodies avoiding diffusion in supernatant, protease degradation or binding on soluble membrane receptors. After cell removal, the captured cytokines are revealed by tracer antibodies and appropriate conjugates.
Principal:
After cell stimulation, locally produced cytokines are captured by a specific monoclonal antibody. After cell lysis, trapped cytokine molecules are revealed by a secondary biotinylated detection antibody, which is in turn recognised by streptavidin conjugated to alkaline phosphatase. PVDF-bottomed-well plates are then incubated with BCIP/NBT substrate. Colored "purple" spots indicate cytokine production by individual cells.
Recognizes natural (pro and mature) human IL1 Beta
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