Anti-IL-18 antibody (ab191860) is a rabbit polyclonal antibody that is used to detect IL-18 in Western Blot, Flow Cytometry, IHC-P. Suitable for Mouse, Rat samples.
- Over 50 publications
Preservative: 0.025% Sodium azide
Constituents: 2.5% BSA, 0.45% Sodium chloride, 0.1% Dibasic monohydrogen potassium phosphate
Flow Cyt | WB | IHC-P | |
---|---|---|---|
Mouse | Expected | Tested | Expected |
Rat | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1.00000-3.00000 µg for 106 Cells | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 0.25000-0.50000 µg/mL | Notes - |
Species Mouse | Dilution info 0.25000-0.50000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 2.00000-5.00000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
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Pro-inflammatory cytokine primarily involved in epithelial barrier repair, polarized T-helper 1 (Th1) cell and natural killer (NK) cell immune responses (PubMed:26638072, PubMed:26638073). Upon binding to IL18R1 and IL18RAP, forms a signaling ternary complex which activates NF-kappa-B, triggering synthesis of inflammatory mediators (By similarity). Synergizes with IL12/interleukin-12 to induce IFNG synthesis from T-helper 1 (Th1) cells and natural killer (NK) cells (By similarity). 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 (PubMed:30392956).
Igif, Il18, Interleukin-18, IL-18, Interferon gamma-inducing factor, Interleukin-1 gamma, IFN-gamma-inducing factor, IL-1 gamma
Anti-IL-18 antibody (ab191860) is a rabbit polyclonal antibody that is used to detect IL-18 in Western Blot, Flow Cytometry, IHC-P. Suitable for Mouse, Rat samples.
- Over 50 publications
Preservative: 0.025% Sodium azide
Constituents: 2.5% BSA, 0.45% Sodium chloride, 0.1% Dibasic monohydrogen potassium phosphate
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Full details and terms and conditions can be found here:
Terms & Conditions.
Flow Cytometry analysis of RH35 cells stained with ab191860 in blue with a concentration of 1μg/1x106 cells; an isotype control antibody (rabbit IgG) in green with a concentration of 1μg/1x106 cells, and an unlabelled sample in red. The secondary antibody used was DyLight®488 conjugated goat anti-rabbit IgG in the concentration 5-10μg/ 1x106 cells.
SDS PAGE performed on 5-20% gel for 2-3 hours.
Proteins were transferred to a nitrocellulose membrane at 150mA for 50-90 minutes and blocked with 5% milk/TBS for 1.5 hours at room temperature.
All lanes: Western blot - Anti-IL-18 antibody (ab191860) at 0.5 µg/mL
Lane 1: mouse spleen tissue lysates at 30 µg/mL
Lane 2: mouse thymus tissue lysates at 30 µg/mL
Lane 3: mouse lung tissue lysates at 30 µg/mL
Lane 4: mouse ANA-1 whole cell lysates at 30 µg/mL
All lanes: goat anti-rabbit IgG-HRP at 1/5000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 22 kDa
Immunohistochemistry analysis of paraffin-embedded section of rat spleen tissue labeling IL-18 antibody with ab191860 at 2μg/mL (incubation: overnight at 4°C). Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
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