Human LILRA4/CD85g/ILT7 Antibody Summary
Glu24-Asn446
Accession # P59901
Applications
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.
Scientific Data
Detection of LILRA4/CD85g/ILT7 in Human PBMCs by Flow Cytometry. Human peripheral blood monocytes were labeled with Mouse Anti-Human LILRA4/CD85g/ILT7 Monoclonal Antibody (Catalog # MAB6287) followed by Allophycocyanin-conjugated Anti-Mouse IgG F(ab')2Secondary Antibody (Catalog # F0101B) and Human DLEC/CLEC4C/BDCA-2 Fluorescein-conjugated Polyclonal Antibody (Catalog # FAB1376F). Quadrant markers were set based on control antibody staining (Catalog # MAB003).
Reconstitution Calculator
Preparation and Storage
- 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: LILRA4/CD85g/ILT7
LILRA4, also known as ILT7 and CD85g, is a 499 amino acid (aa) type I transmembrane glycoprotein that contains four Ig-like domains in its extracellular region. LILRA4 is selectively expressed on plasmacytoid dendritic cells (pDC). It binds to BST2/CD317 on bone marrow stromal cells and associates with the gamma subunit of Fc epsilon RI. This receptor complex transmits signals that inhibit the TLR-induced production of type I interferon. The LILRA4-mediated interactions between pDC and tumor cells similarly inhibit the production of proinflammatory cytokines and contribute to reduced anti-tumor immune responses. Alternate splicing of human LILRA4 generates an isoform that lacks the N-terminal 43 aa of the extracellular domain.
Product Datasheets
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