Mouse IL-33 PE-conjugated Antibody (2024)

Catalog #: IC3626P
8 Citations 2 Reviews Datasheet / COA / SDS

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Citations (8)

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Mouse IL-33 PE-conjugated Antibody Summary

Species Reactivity

Mouse

Specificity

Detects mouse IL-33 in direct ELISAs.

Source

Monoclonal Rat IgG_2A Clone # 396118

Purification

Protein A or G purified from hybridoma culture supernatant

Immunogen

E. coli-derived recombinant mouse IL-33
Ser109-Ile266
Accession # Q8BVZ5

Formulation

Supplied in a saline solution containing BSA and Sodium Azide.

Label

Phycoerythrin (Excitation= 488 nm, Emission= 565-605 nm)

Applications

Recommended Concentration

Sample

Scientific Data

Intracellular Staining by Flow Cytometry View Larger

Detection of IL‑33 in bEnd.3 Mouse Cell Line by Flow Cytometry. bEnd.3 mouse endothelioma cell line was stained with Rat Anti-Mouse IL-33 PE-conjugated Mono-clonal Antibody (Catalog # IC3626P, filled histogram) or isotype control antibody (Catalog # IC006P, open histogram). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005). View our protocol for Staining Intracellular Molecules.

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Preparation and Storage

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Protect from light. Do not freeze.

12 months from date of receipt, 2 to 8 °C as supplied.

Background: IL-33

IL-33, also known as NF-HEV and DVS 27, is a 30 kDa proinflammatory protein that may also regulate gene transcription (1-3). DVS 27 was identifed as a gene that is upregulated in vasospastic cerebral arteries (1). NF-HEV was described as a nuclear factor that is preferentially expressed in the endothelial cells of high endothelial venules relative to endothelial cells from other tissues (2). IL-33 was identified based on sequence and structural hom*ology with IL-1 family cytokines (3). DVS 27, NF-HEV, and IL-33 share 100% amino acid sequence identity. IL-33 is constitutively expressed in smooth muscle and airway epithelia. It is upregulated in arterial smooth muscle, dermal fibroblasts, and keratinocytes following IL-1 alpha or IL-1 beta stimulation (1, 3). Similar to IL-1, IL-33 can be cleaved in vitro by caspase-1, generating an N-terminal fragment that is slightly shorter than the C-terminal fragment (3, 4). The N-terminal portion of full length IL-33 contains a predicted bipartite nuclear localization sequence and a homeodomain-like helix-turn-helix DNA binding domain. By immunofluorescence, full length IL-33 localizes to the nucleus in HUVECs and transfectants (2). The C-terminal fragment, corresponding to mature IL-33, binds and triggers signaling through mast cell IL-1 R4/ST2L, a longtime orphan receptor involved in the augmentation of Th2 cell responses (3, 5-7). A ternary signaling complex is formed by the subsequent association of IL-33 and ST2L with IL-1R AcP (8). Stimulation of Th2 polarized lymphocytes with mature IL-33 in vitro induces IL-5 and IL-13 secretion (3). In vivo administration of mature IL-33 promotes increased production of IL-5, IL-13, IgE, and IgA, as well as splenomegaly and inflammatory infiltration of mucosal tissues (3). Full length and mature mouse IL-33 share approximately 55% and 90% amino acid (aa) sequence identity with human and rat IL-33, respectively. Mouse IL-33 shares less than 25% aa sequence identity with other IL-1 family proteins.

References

Onda, H. et al. (1999) J. Cereb. Blood Flow Metab. 19:1279.
Baekkevold, E.S. et al. (2003) Am. J. Pathol. 163:69.
Schmitz, J. et al. (2005) Immunity 23:479.
Black, R.A. et al. (1989) J. Biol. Chem. 264:5323.
Xu, D. et al. (1998) J. Exp. Med. 187:787.
Lohning, M. et al. (1998) Proc. Natl. Acad. Sci. USA95:6930.
Dinarello, C.A. (2005) Immunity 23:461.
Chackerian, A.A. et al. (2007) J. Immunol. 179:2551.

Long Name

Interleukin 33

Entrez Gene IDs

90865 (Human); 77125 (Mouse)

Alternate Names

C9orf26; C9orf26chromosome 9 open reading frame 26 (NF-HEV); DKFZp586H0523; DVS27; DVS27-related protein; IL1F11; IL-1F11; IL33; IL-33; interleukin 33; Interleukin-1 family member 11; interleukin-33; NFHEV; NF-HEV; NF-HEVNFEHEV; Nuclear factor from high endothelial venules; RP11-575C20.2

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Related Research Areas

Group 2 ILCs
IL-1 Family
Molecules Secreted by VSMC
Multiple Sclerosis and Myelin Related Molecules
Search Cytokine and Growth Factor Products
T Cell Cytokine Signaling
Th2 Cells

Citations for Mouse IL-33 PE-conjugated Antibody

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

8 Citations: Showing 1 - 8
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Macrophages regulate lung ILC2 activation via Pla2g5-dependent mechanisms
Authors: M Yamaguchi, SK Samuchiwal, O Quehenberg, JA Boyce, B Balestrier
Mucosal Immunol, 2017-12-20;11(3):615-626.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
IL-33/ST2-mediated inflammation in macrophages is directly abrogated by IL-10 during rheumatoid arthritis
Authors: S Chen, B Chen, Z Wen, Z Huang, L Ye
Oncotarget, 2017-05-16;8(20):32407-32418.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry, ICC
Dopaminergic Toxin 1-Methyl-4-Phenylpyridinium, Proteins alpha-Synuclein and Glia Maturation Factor Activate Mast Cells and Release Inflammatory Mediators.
Authors: Kempuraj D, Thangavel R, Yang E, Pattani S, Zaheer S, Santillan D, Santillan M, Zaheer A
PLoS ONE, 2015-08-14;10(8):e0135776.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
Type II cytokines impair host defense against an intracellular fungal pathogen by amplifying macrophage generation of IL-33.
Authors: Verma, A, Kroetz, D N, Tweedle, J L, Deepe, G S Jr
Mucosal Immunol, 2014-08-13;8(2):380-9.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
IL-33 targeting attenuates intestinal mucositis and enhances effective tumor chemotherapy in mice.
Authors: Guabiraba R, Besnard A, Menezes G, Secher T, Jabir M, Amaral S, Braun H, Lima-Junior R, Ribeiro R, Cunha F, Teixeira M, Beyaert R, Graham G, Liew F
Mucosal Immunol, 2014-01-15;7(5):1079-93.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
Murine mast cells secrete and respond to interleukin-33.
Authors: Tung, Hui-Ying, Plunkett, Beverly, Huang, Shau-Ku, Zhou, Yufeng
J Interferon Cytokine Res, 2013-09-12;34(3):141-7.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
Interleukin-33 and alveolar macrophages contribute to the mechanisms underlying the exacerbation of IgE-mediated airway inflammation and remodelling in mice.
Authors: Mizutani N, Nabe T, Yoshino S
Immunology, 2013-06-01;139(2):205-18.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
Trefoil factor 2 rapidly induces interleukin 33 to promote type 2 immunity during allergic asthma and hookworm infection.
Authors: Wills-Karp M, Rani R, Dienger K
J. Exp. Med., 2012-02-13;209(3):607-22.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry

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Reviews for Mouse IL-33 PE-conjugated Antibody

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Mouse IL-33 PE-conjugated Antibody

By Anonymous on 08/30/2016

Application: Flow Sample Tested: Lung single-cell suspension Species: Mouse

Cells were activated with PMA and ionomycin for 2 hrs before intracellular staining.

Mouse IL-33 PE-conjugated Antibody

By Oliver Burton on 07/25/2016

Application: Flow Sample Tested: mast cells Species: Mouse

Mast cells were cultured from the bone marrow of IL-33-deficient or WT C57BL/6 mice. Genotypes were confirmed by PCR. Cells (5x10^5) were stained for viability, FceRI and c-kit, blocking Fc receptors, then fixed with BD Cytofix/Cytoperm. Cells were permeabilized with BD Permeabilization Buffer, and stained with 2ul anti-mouse IL-33-PE or rat IgG2a-PE isotype control. Cells were washed three times, and data were acquired on a BD FACSCanto LSR flow cytometer, gating on live c-Kit+FceRI+ cells.

Fluorescence increases by two orders of magnitude in both WT and IL-33-KO cells following staining with the IL-33-PE antibody relative to the isotype control. I am currently investigating whether there is any specific signal after stimulation of the cells, at which point IL-33 is induced. Staining with the recommended (greater) amount of antibody produces an even greater background shift in unstimulated cells.

R&D Systems Technical Service is investigating.