Render Target: SSR
Render Timestamp: 2025-02-20T18:44:45.646Z
Commit: 7500bcdc731e9059bbdfbdbe9e72caa896e426e8
XML generation date: 2024-09-30 01:58:55.990
Product last modified at: 2025-01-24T22:30:10.339Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

MXRA8 (E7K5Q) Rabbit mAb #56572

Filter:
  • WB

    Supporting Data

    REACTIVITY H Mk
    SENSITIVITY Endogenous
    MW (kDa) 48-62
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    Species Cross-Reactivity Key:
    • H-Human 
    • Mk-Monkey 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    MXRA8 (E7K5Q) Rabbit mAb recognizes endogenous levels of total MXRA8 protein.

    Species Reactivity:

    Human, Monkey

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human MXRA8 protein.

    Background

    MXRA8 (Matrix remodeling-associated protein 8), also known as DICAM or limitrin, is a dual immunoglobulin domain containing cell adhesion molecule expressed on epithelial, myeloid, and mesenchymal cells. A single-pass type I transmembrane protein that is highly expressed at areas of cell-cell contact and may localize to tight junctions, MXRA8 mediates cell adhesion via interaction with αVβ3 integrin (1). Through its interactions with integrins, MXRA8 has been shown to suppress both angiogenesis (2) and osteoclast differentiation (3) in vitro by attenuating p38 mitogen-activated protein (MAP) kinase signaling. MXRA8 also plays a pivotal role in ferroptosis and the immune microenvironment of glioma, suggesting that it may serve as a novel prognostic marker and therapeutic target (4). A recent study showed that multiple emerging arthritogenic alphaviruses, including CHIKV, RRV, MAYV, and ONNV, use MXRA8 as a functional receptor (5). Structural insights into how Chikungunya virus particles bind MXRA8 to enhance viral attachment and internalization into cells may provide a guide for developing antiviral therapies against arthritogenic alphaviruses (6).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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