Cell Signaling Technology Logo
1% for the planet logo
Trial Size Available Flag
Recombinant Flag
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

CLEC4A (F2X3I) Rabbit mAb #76213

Filter:
  • WB
  • F

    Supporting Data

    REACTIVITY H
    SENSITIVITY Endogenous
    MW (kDa) 30-40
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • F-Flow Cytometry 
    Species Cross-Reactivity Key:
    • H-Human 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000
    Flow Cytometry (Live) 1:100 - 1:400

    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

    CLEC4A (F2X3I) Rabbit mAb recognizes endogenous levels of total CLEC4A protein. This antibody detects a 65 kDa and a 100 kDa protein of unknown identity in some cell lines.

    Species Reactivity:

    Human

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asn200 of human CLEC4A protein.

    Background

    C-type lectin domain family 4 member A (CLEC4A), also referred to as dendritic cell (DC) immunoreceptor (DCIR), is a type II membrane glycoprotein, primarily expressed on myeloid-derived cells including monocytes, DCs, macrophages, and neutrophils (1-4). CLEC4A contains an ITIM motif in the cytoplasmic domain, which is involved in regulating immune response (1,2,5). CLEC4A provides anti-inflammatory signaling through the recruitment of phosphatases SHP-1 and SHP-2 (3-5). Insufficient CLEC4A function might cause autoimmune diseases, such as rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) (4,5).
    For Research Use Only. Not For Use In Diagnostic Procedures.
    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit our Trademark Information page.