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Description
Research Area
Images & Validation
−| Tested Applications | ELISA, IF, IHC, IP, WB |
|---|---|
| Dilution Range | ELISA: 1:1,000 - 1:5,000, IHC: 1:50-1:250, IF: 1:50-1:250, IP: 1:200-1:800, WB: 1:500 - 1:2,000 |
| Reactivity | Mouse |
| Application Notes |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Immunogen | This antibody was prepared by repeated immunizations with recombinant mouse IL-1ß produced in E.coli. The MW of recombinant mouse IL-1ß was 17 kDa. |
| Target | Il1b |
| Purity | This is an IgG preparation of whole rabbit serum purified by DEAE fractionation. This antibody is primarily directed against mature, 17,000 MW mouse IL-1ß and is useful in determining its presence in various assays. The antibody does not recognize human IL-1ß or mouse IL-1α based on a neutralization assay. In ELISA formats and other immunoreactive assays, reactivity occurs with rat IL-1ß. This antibody will recognize 10% of the non-denatured (native) precursor 31,000 MW mouse IL-1ß containing samples but will primarily detect all of the 17,000 MW mature molecule. However, in immunoblot analysis, the usual procedure of heating the sample in SDS with or without reducing agents will facilitate denaturing of the 31,000 MW IL- 1ß precursor molecule. Denatured 31,000 precursor IL-1ß will be recognized by this antibody. |
| Conjugation | Unconjugated |
Storage & Handling
−| Storage | Store Anti-IL-1 beta antibody at 4° C prior to restoration. For extended storage aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. |
|---|---|
| Form/Appearance | Lyophilized |
| Buffer/Preservatives | Preservative: None. Stabilizer: None; Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2 |
| Concentration | 1.0 mg/mL |
| Expiration Date | 12 months from date of receipt. |
| Disclaimer | For research use only |
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Immunofluorescence microscopy after staining of mouse carotid artery tissue with anti-Mouse IL-1ß antiserum diluted 1:50. Tissue sections were prepared after cryofixation. Reaction occurred at room temperature for 60' followed by washes and reaction with Rhodamine conjugated Gt-a-Rabbit IgG (p/n orb347644). Tissue was counterstained with bis-benzimide solution at 0.5 mg/ml in PBS for 15 min at room temperature. Panel A) shows no antibody staining of WT uninjured mouse carotid tissue. Panel B) shows anti-IL-1ß staining of cells after surgical injury of tissue. Panel C) shows no antibody staining of injured carotid tissue from an IL-1ß KO mouse.

Immunohistochemistry of Rabbit anti-IL1Beta Antibody in Mouse Embryonic Kidney Tissue: Mouse Embryonic Kidney Fixation: FFPE buffered formalin 10% conc Ag Retrieval: Heat, Citrate pH6.2. Pressure Cooker Primary antibody: 2 ug/ml 1.5 hour @ room T Secondary Ab: MACH 1 HRP POLYMER 1:50 45" RT

This antibody will recognize 10% of the non-denatured (native) precursor 31000 MW mouse IL-1ß containing samples but will primarily detect all of the 17000 MW mature molecule. However, in western blot analysis, the usual procedure of heating the sample in SDS with or without reducing agents will facilitate denaturing of the 31, 000 MW IL- 1ß precursor molecule. Denatured IL-1ß will have a 18 kDa band.
Quick Database Links
UniProt Details
−NCBI Reference Sequences
−| RefSeq | CAA28637.1 |
|---|
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Protocol Information
Il1b Antibody (orb345217)
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