Human IL-20R alpha PE-conjugated Antibody Summary
Accession # Q9UHF4
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Detection of IL‑20 R alpha in T47D Cell Line by Flow Cytometry. T47D human breast duct carcinoma cell line was stained with Mouse Anti-Human IL-20 Ra PE-conjugated Monoclonal Antibody (Catalog # FAB11762P, filled histogram) or isotype control antibody (IC002P, open histogram). Staining was performed using our View our Staining Membrane-associated Proteins protocol.
Detection of IL‑20 R alpha in BaF3 Mouse Cell Line Transfected with Human IL‑20 R alpha and eGFP by Flow Cytometry. BaF3 mouse pro-B cell line transfected with human IL-20 Ra and eGFP was stained with Mouse Anti-Human IL-20 Ra PE-conjugated Monoclonal Antibody (Catalog # FAB11762P). Quadrant markers were set based on control antibody staining (Catalog # IC002P). View our protocol for Staining Membrane-associated Proteins.
Preparation and Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: IL-20R alpha
IL-20 receptor alpha (IL-20 R alpha ), also named IL-20 R1, CRF2-8, and ZCYTOR7, belongs to the class II cytokine receptor family, which includes 12 members. These receptors are characterized by the patterns of conserved amino acid (aa) residues in their extracellular domains, which are composed of tandem fibronectin type III domains (1). Class II cytokine receptors form heterodimeric signaling receptor complexes that mediate class II cytokine signals. Subunits of the different receptor complexes are shared and serve multiple functions (1).
The gene for human IL-20 R alpha is mapped to chromosome 6 and encodes a 553 aa glycoprotein with a 29 aa signal peptide, a 221 aa extracellular domain, a 24 aa transmembrane region and a 279 aa intracellular domain (2). IL-20 R alpha is widely expressed and is detected at high levels in multiple tissues including skin, testis, heart, placenta, salivary gland and prostate gland (1). The expression of IL-20 R alpha, together with that of IL-20 R beta, is upregulated in psoriatic skin lesions on keratinocytes, immune cells, and endothelial cells (1, 2).
IL-20 R alpha heterodimerizes with IL-20 R beta to form the functional receptor that mediates IL-19, IL-20 and IL-24 signals (3, 4). IL-20 R alpha also heterodimerizes with IL-10 R beta to form the functional receptor complex for IL-26 (5). Binding of these IL-10 family class II cytokines to their functional receptors induces activation of the JAK-STAT signal transduction pathway. At low ligand concentrations, STAT3 has been shown to be the predominant STAT proteins activated through either complexes (3‑5).
- Kotenko, S.V. (2003) Cytokine & Growth Factor Reviews 13:223.
- Xie, M.H. et al. (2000) J. Biol. Chem. 275:31335.
- Dumoutier, L. et al. (2001) J. Immunol. 167:3534.
- Parrish-Novak, J. et al. (2002) J. Biol. Chem. 277:47517s.
- Sheikh. F. et al. (2004) J. Immunol. 172:2006.
Citation for Human IL-20R alpha 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.
1 Citation: Showing 1 - 1
Interleukin-24 inhibits the plasma cell differentiation program in human germinal center B cells.
Authors: Maarof G, Bouchet-Delbos L, Gary-Gouy H, Durand-Gasselin I, Krzysiek R, Dalloul A
Sample Types: Whole Cells
Applications: Flow Cytometry
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