Mouse IL-1 beta ELISA Kit, Fluorescent is a single-wash 90-min Simplestep used to quantify Mouse IL-1 beta with a sensitivity of 0.2 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Fluorescent Sandwich ELISA - 530/570/590 nm readout : works on any standard plate reader
- Cited in over 5 citations
Application | Reactivity | Dilution info | Notes |
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Application sELISA | Reactivity Reacts | Dilution info - | Notes - |
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Potent pro-inflammatory 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. Plays a role in angiogenesis by inducing VEGF production synergistically with TNF and IL6. Involved in transduction of inflammation downstream of pyroptosis: its mature form is specifically released in the extracellular milieu by passing through the gasdermin-D (GSDMD) pore.
Interleukin-1 beta, IL-1 beta, Il1b
Mouse IL-1 beta ELISA Kit, Fluorescent is a single-wash 90-min Simplestep used to quantify Mouse IL-1 beta with a sensitivity of 0.2 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Fluorescent Sandwich ELISA - 530/570/590 nm readout : works on any standard plate reader
- Cited in over 5 citations
Sample | n | C.V. |
---|---|---|
Sample Cell Media | n 5 | C.V. 6.1 |
Sample | n | C.V. |
---|---|---|
Sample Cell Media | n 3 | C.V. 7.7 |
Sample type | Average % | Range |
---|---|---|
Sample type Cell culture supernatant | Average % = 105 | Range 100 - 108 % |
Sample type Serum | Average % = 101 | Range 98 - 103 % |
Sample type Urine | Average % = 94 | Range 91 - 95 % |
Sample type Plasma | Average % = 89 | Range 78 - 95 % |
Sample type Tissue Homogenate | Average % = 97 | Range 95 - 100 % |
IL-1 beta (Interleukin-1 beta) in vitro CatchPoint SimpleStep ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the quantitative measurement of IL-1 beta (Interleukin-1 beta) protein in mouse serum, plasma, urine, cell culture supernatant, and cell and tissue extracts.
This CatchPoint SimpleStep ELISA kit has been optimized for Molecular Devices Microplate Readers. Click here for a list of recommended Microplate Readers.
If using a Molecular Devices' plate reader supported by SoftMax® Pro software, a preconfigured protocol for these CatchPoint SimpleStep ELISA Kits is available with all the protocol and analysis settings at www.softmaxpro.org.
The CatchPoint SimpleStep ELISA employs an affinity tag labeled capture antibody and a reporter conjugated detector antibody which immunocapture the sample analyte in solution. This entire complex (capture antibody/analyte/detector antibody) is in turn immobilized via immunoaffinity of an anti-tag antibody coating the well. To perform the assay, samples or standards are added to the wells, followed by the antibody mix. After incubation, the wells are washed to remove unbound material. CatchPoint HRP Development Solution containing the Stoplight Red Substrate is added. During incubation, the substrate is catalyzed by HRP generating a fluorescent product. Signal is generated proportionally to the amount of bound analyte and the intensity is measured in a fluorescence plater reader at 530/570/590 nm Excitation/Cutoff/Emission.
Interleukin-1 beta (IL-1 beta) is a 17.5 kDa cytokine protein of the Interleukin 1 family. IL-1 beta is secreted by macrophages and other cell types in response to inflammatory agents or infection. IL-1 beta plays a role in a number of cellular processes, including immune responses, bone remodeling, apoptosis and inflammatory pain hypersensitivity.
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Example of mouse IL-1 beta (Interleukin-1 beta) standard curve in Sample Diluent NS.
Background-subtracted data values (mean +/- SD) are graphed.
Comparison of secreted mouse IL-1 beta in unstimulated and LPS stimulated RAW264.7 cells.
RAW264.7 cells were grown in the absence (unstimulated) or presence of 5 μg/mL Lipopolysaccharide (LPS) (stimulated) for 48 hours. IL-1 beta was measured in 2-fold diluted cell culture supernatants of unstimulated and LPS stimulated RAW264.7 and cell culture media. Measured values were interpolated from the IL-1 beta Standard Curve diluted in Sample Diluent NS and corrected for dilution factor. Mean of duplicate values +/-SD are graphed: 1.1 pg/mL unstimulated, 83.5 pg/mL stimulated. There was no detectable signal in media.
Demonstration of the linearity of dilution by the titration of RAW264.7 stimulated for 48 hours with LPS undiluted to 32-fold dilution in Sample Diluent NS. Background-subtracted data values (mean +/- SD, n = 2) are graphed.
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