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Flow cytometric analysis of CD85j expression on human peripheral lymphocytes. Whole blood was stained with either Purified Mouse Anti-Human CD85j (Cat. No. 555941; solid line histogram) or Purified Mouse IgG2b κ Isotype Control (Cat. No. 555740; dashed line histogram), followed by FITC Goat Anti-Mouse IgG/IgM (Cat. No. 555988). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes.
Flow cytometric analysis of CD85j expression on human peripheral lymphocytes. Whole blood was stained with either Purified Mouse Anti-Human CD85j (Cat. No. 555941; solid line histogram) or Purified Mouse IgG2b κ Isotype Control (Cat. No. 555740; dashed line histogram), followed by FITC Goat Anti-Mouse IgG/IgM (Cat. No. 555988). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes.
Flow cytometric analysis of CD85j expression on human peripheral lymphocytes. Whole blood was stained with either Purified Mouse Anti-Human CD85j (Cat. No. 555941; solid line histogram) or Purified Mouse IgG2b κ Isotype Control (Cat. No. 555740; dashed line histogram), followed by FITC Goat Anti-Mouse IgG/IgM (Cat. No. 555988). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes.
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CD85 molecules belong to a large immunoregulatory family and it has been clustered into different subclasses from CD85a to CD85m in the VIIth HLDA workshop. CD85j is also called as Ig-like transcript (ILT2), or leukocyte Ig-like receptor (LIR-1). Reacts with an 110 kDa membrane glycoprotein expressed on a subset of NK cells, which varies amongst individuals, and a subpopulation of T lymphocytes. Expression on T lymphocytes, NK cells may depend on the individuals tested. Function studies show that ligation of ILT2 with MHC class I including HLA-A, B, G1 and -E induces an inhibitory signal via recruitment of SHP-1 phosphatase.
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