Home / IL-22 R alpha 1 / Mouse IL-22 R alpha 1 Antibody

Mouse IL-22 R alpha 1 Antibody

Catalog #: MAB4294
3 Citations Datasheet / COA / SDS
Catalog # Availability Size / Price Qty
MAB4294
MAB4294-SP
Product Details
Citations (3)
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Summary Preparation and Storage Reconstitution Calculator Background Product Datasheets Related Research Areas

Mouse IL-22 R alpha 1 Antibody Summary

Species Reactivity
Mouse
Specificity
Detects mouse IL-22 R alpha 1 in direct ELISAs and Western blots. Shows approximately 20% cross‑reactivity with recombinant human (rh) IL-22 R and no cross-reactivity with rhIL-20 R alpha, rhIL-20 R beta, or recombinant mouse IL-22BP.
Source
Monoclonal Rat IgG2A Clone # 496504
Purification
Protein A or G purified from hybridoma culture supernatant
Immunogen
Mouse myeloma cell line NS0-derived recombinant mouse IL-22 R alpha 1
Thr18-Ala228
Accession # Q80XZ4
Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Applications

Recommended Concentration
Sample
Western Blot
1 µg/mL
Recombinant Mouse IL‑22 R alpha 1 (Catalog # 4294-MR)

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.

Reconstitution Calculator

Reconstitution Calculator

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Preparation and Storage

Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS.
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Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 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.

Background: IL-22 R alpha 1

The IL-22 receptor, also known as IL-22 R alpha 1 and CRF2-9, is an approximately 65 kDa type I transmembrane glycoprotein that belongs to the type II cytokine receptor family (CRF). IL-22 R alpha 1 contains a 211 amino acid (aa) extracellular domain (ECD) with two fibronectin type III repeats, and a 330 aa cytoplasmic domain (1). Within the ECD, mouse IL-22 R alpha 1 shares 78%, 78%, and 94% aa sequence identity with canine, human, and rat IL-22 R alpha 1, respectively. It shares 20% - 26% aa sequence identity with the ECDs of other class II receptors IL-10 R, IL-20 R, and IL-28 R. IL-22 R alpha 1 associates with either IL-10 R beta or IL-20 R beta to form receptor complexes with distinct ligand selectivities. IL-10 R beta is a shared subunit of the IL-10, -22, -26, -28, and -29 receptors, while IL-20 R beta is a shared subunit of the IL-19, -20, -22, and -24 receptors (2). IL-22 R alpha 1/IL-10 R beta is an IL-22 responsive receptor (3, 4), and IL-22 R alpha 1/IL-20 R beta is an IL-20 or IL-24 responsive receptor (5, 6). In both cases, IL‑22 R alpha 1 functions as the high affinity ligand binding subunit, and subsequent association with IL-10 R beta or IL-20 R beta serves to stabilize the complex (3, 6 - 9). IL‑22 R alpha 1 contains cytoplasmic motifs for interactions with signal transduction molecules, but association with IL-10 R beta or IL-20 R beta is required for signal transduction (3, 7). IL-22BP functions as a competitive antagonist by binding IL-22 and preventing its association with IL-22 R alpha 1 (8, 10). Even though it is a receptor for interleukins, IL‑22 R alpha 1 is not expressed on hematopoietic cells (7, 11, 12). Instead, IL-22 R alpha 1 expression is restricted to epithelial and stromal cells (7, 11 - 14). IL‑22 R alpha 1 signaling promotes innate immune responses and wound healing at sites of infection and inflammation. This includes upregulation of antimicrobial, acute phase, proinflammatory, and extracellular matrix proteins as well as proteases (4, 12, 14, 15). IL-22 R alpha 1 signaling also promotes downregulation of proteins involved in keratinocyte differentiation (4, 15).

References
  1. Tachiiri, A. et al. (2003) Genes Immun. 4:153.
  2. Langer, J.A. et al. (2004) Cytokine Growth Factor Rev. 15:33. 
  3. Xie, M-H. et al. (2000) J. Biol. Chem. 275:31335. 
  4. Boniface, K. et al. (2005) J. Immunol. 174:3695. 
  5. Dumoutier, L. et al. (2001) J. Immunol. 167:3545. 
  6. Wang, M. et al. (2002) J. Biol. Chem. 277:7341. 
  7. Kotenko, S.V. et al. (2001) J. Biol. Chem. 276:2725. 
  8. Li, J. et al. (2004) Int. Immunopharmacol. 4:693.
  9. Logsdon, N.J. et al. (2002) J. Interferon Cytokine Res. 22:1099
  10. Kotenko, S.V. et al. (2001) J. Immunol. 166:7096.
  11. Nagalakshmi, M.L. et al. (2004) Int. Immunopharmacol. 4:577.
  12. Nagalakshmi, M.L. et al. (2004) Int. Immunopharmacol. 4:679.
  13. Aggarwal, S. et al. (2001) J. Interferon Cytokine Res. 21:1047.
  14. Wolk, K. et al. (2004) Immunity 21:241.
  15. Wolk, K. et al. (2006) Eur. J. Immunol. 36:1309.
Long Name
Interleukin 22 Receptor
Entrez Gene IDs
58985 (Human); 230828 (Mouse)
Alternate Names
CRF2-9; CRF2-9interleukin 22 receptor; Cytokine receptor class-II member 9; Cytokine receptor family 2 member 9; IL-22 R alpha 1; IL-22 receptor subunit alpha-1; IL22R alpha 1; IL22R; IL22R1; IL22RA1; IL-22Ra1; IL-22R-alpha-1; IL-TIF-R1; interleukin 22 receptor, alpha 1; interleukin-22 receptor subunit alpha-1; zcytoR11

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Citations for Mouse IL-22 R alpha 1 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.

3 Citations: Showing 1 - 3
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  1. Murine astrocytes produce IL-24 and are susceptible to the immunosuppressive effects of this cytokine
    Authors: AR Burmeister, MB Johnson, JJ Yaemmongko, I Marriott
    J Neuroinflammation, 2019-03-02;16(1):55.
    Species: Mouse
    Sample Types: Cell Lysates
    Applications: Western Blot
  2. IL-22 signaling contributes to West Nile encephalitis pathogenesis.
    Authors: Wang, Penghua, Bai, Fengwei, Zenewicz, Lauren A, Dai, Jianfeng, Gate, David, Cheng, Gong, Yang, Long, Qian, Feng, Yuan, Xiaoling, Montgomery, Ruth R, Flavell, Richard, Town, Terrence, Fikrig, Erol
    PLoS ONE, 2012-08-28;7(8):e44153.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Neutralization
  3. IL-23-Mediated Epidermal Hyperplasia Is Dependent on IL-6.
    Authors: Lindroos J, Svensson L, Norsgaard H
    J. Invest. Dermatol., 2011-02-03;131(5):1110-8.
    Species: Mouse
    Sample Types: Tissue Homogenates
    Applications: Western Blot

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