IL-1 is a name that designates two pleiotropic cytokines, IL-1 alpha (IL-1F1) and IL-1 beta (IL-1F2), which are the products of distinct genes. IL-1 alpha and IL-1 beta are structurally related polypeptides that share approximately 27% amino acid (aa) identity in feline. Both proteins are produced by a wide variety of cells in response to inflammatory agents, infections, or microbial endotoxins. While IL-1 alpha and IL-1 beta are regulated independently, they bind to the same receptor and exert identical biological effects. IL‑1 RI binds directly to IL-1 alpha or IL-1 beta and then associates with the IL-1 R accessory protein (IL-1 R3/IL-1 R AcP) to form a high-affinity receptor complex that is competent for signal transduction. IL-1 RII has high affinity for IL-1 beta but functions as a decoy receptor and negative regulator of IL-1 beta activity. IL-1ra functions as a competitive antagonist by preventing IL-1 alpha and IL-1 beta from interacting with IL-1 RI (1‑4). The feline IL-1 beta cDNA encodes a 267 aa precursor. A 115 aa propeptide is cleaved intracellularly by the cysteine protease IL-1 beta -converting enzyme (Caspase-1/ICE) to generate the active cytokine (5, 6). The 17 kDa mature feline IL-1 beta shares 63%‑78% aa sequence identity with canine, cotton rat, equine, human, mouse, porcine, rat, and rhesus IL-1 beta.
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Key Product Details
Species Reactivity
Applications
Label
Antibody Source
Product Specifications
Immunogen
Ala116-Ser267
Accession # P41687
Specificity
Clonality
Host
Isotype
Endotoxin Level
Scientific Data Images for Feline IL-1 beta/IL-1F2 Antibody
Cell Proliferation Induced by IL‑1 beta /IL‑1F2 and Neutral-ization by Feline IL‑1 beta /IL‑1F2 Antibody.
Recombinant Feline IL-1 beta /IL-1F2 (Catalog # 1796-FL) stimulates proliferation in the the D10.G4.1 mouse helper T cell line in a dose-dependent manner (orange line). Proliferation elicited by Recombinant Feline IL-1 beta /IL-1F2 (50 pg/mL) is neutralized (green line) by increasing concen-trations of Goat Anti-Feline IL-1 beta /IL-1F2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1796). The ND50 is typically 0.02-0.08 µg/mL.Feline IL-1 beta / IL-1F2 ELISA Standard Curve
Recombinant Feline IL‑1 beta /IL‑1F2 (Catalog # 1796-FL) was serially diluted and captured by Goat Anti-Feline IL‑1 beta /IL‑1F2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1796) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Feline IL‑1 beta /IL‑1F2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1796) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)Feline IL-1 beta / IL-1F2 ELISA Standard Curve
Recombinant Feline IL‑1 beta /IL‑1F2 (Catalog # 1796-FL) was serially diluted and captured by Goat Anti-Feline IL‑1 beta /IL‑1F2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1796) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Feline IL‑1 beta /IL‑1F2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1796) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)Applications for Feline IL-1 beta/IL-1F2 Antibody
Immunocytochemistry
Sample: Immersion fixed feline peripheral blood mononuclear cells
Western Blot
Sample: Recombinant Feline IL‑1 beta /IL‑1F2 (Catalog # 1796-FL)
Neutralization
Feline IL-1 beta /IL-1F2 Sandwich Immunoassay
Reviewed Applications
Read 1 review rated 4 using AF1796 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: IL-1 beta/IL-1F2
References
- Allan, S.M. et al. (2005) Nat. Rev. Immunol. 5:629.
- Boraschi, D. and A. Tagliabue (2006) Vitam. Horm. 74:229.
- Kornman, K.S. (2006) Am. J. Clin. Nutr. 83:475S.
- Isoda, K. and F. Ohsuzu (2006) J. Atheroscler. Thromb. 13:21.
- Accession # AAA30814.
- Martinon, F. and J. Tschopp (2007) Cell Death Differ. 14:10.
Long Name
Alternate Names
Entrez Gene IDs
Gene Symbol
UniProt
Additional IL-1 beta/IL-1F2 Products
Product Documents for Feline IL-1 beta/IL-1F2 Antibody
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Feline IL-1 beta/IL-1F2 Antibody
For research use only
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Customer Images
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Application: Immunohistochemistry-FrozenSample Tested: brain and spinal cordSpecies: FelineVerified Customer | Posted 11/16/2018Image was captured using AxioVision fluorescent microscope. IL1B on feline section is highlighted as red while DAPI nuclear counter staining shows blue signal.AF1796 antibody was used at 1:200 dilution.
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars