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Human Monoclonal CD226 Primary Antibody for FACS - ABIN4896040
Brunetta, Fogli, Varchetta, Bozzo, Hudspeth, Marcenaro, Moretta, Mavilio: The decreased expression of Siglec-7 represents an early marker of dysfunctional natural killer-cell subsets associated with high levels of HIV-1 viremia. in Blood 2009
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Human Monoclonal CD226 Primary Antibody for FACS - ABIN2689098
Shibuya, Campbell, Hannum, Yssel, Franz-Bacon, McClanahan, Kitamura, Nicholl, Sutherland, Lanier, Phillips: DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytes. in Immunity 1996
Human Monoclonal CD226 Primary Antibody for CyTOF, FACS - ABIN4899392
Magnani, Alberigo, Bacchetta, Serafini, Andreani, Roncarolo, Gregori: Killing of myeloid APCs via HLA class I, CD2 and CD226 defines a novel mechanism of suppression by human Tr1 cells. in European journal of immunology 2011
Human Monoclonal CD226 Primary Antibody for FACS - ABIN2479330
Fretz, Stark, Metz, Elizondo, Weissleder, Shen, Wittenberg, Simeone, Ferrucci: Detection of hepatic metastases: comparison of contrast-enhanced CT, unenhanced MR imaging, and iron oxide-enhanced MR imaging. in AJR. American journal of roentgenology 1990
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Human Monoclonal CD226 Primary Antibody for FACS, IP - ABIN2479326
Shibuya, Lanier, Phillips: Protein kinase C is involved in the regulation of both signaling and adhesion mediated by DNAX accessory molecule-1 receptor. in Journal of immunology (Baltimore, Md. : 1950) 1998
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Human Monoclonal CD226 Primary Antibody for Func, FACS - ABIN2479328
Kojima, Kanada, Shimizu, Kasama, Shibuya, Nakauchi, Nagasawa, Shibuya: CD226 mediates platelet and megakaryocytic cell adhesion to vascular endothelial cells. in The Journal of biological chemistry 2003
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Human Monoclonal CD226 Primary Antibody for FACS - ABIN4896039
Liu, Qian, Chen, Xu, Gao, Zhang, Zhang, Qi, Gao, Yan: Crystal structure of cell adhesion molecule nectin-2/CD112 and its binding to immune receptor DNAM-1/CD226. in Journal of immunology (Baltimore, Md. : 1950) 2012
Results indicate that low-grade inflammation coupled with elevated blood glucose increases CD226 expression, resulting in decreased endothelial cell glucose uptake in T2DM.
Data show that the severity experimental autoimmune encephalomyelitis (EAE) were reduced and the serum IL-10 (show IL10 Antibodies) expression levels were increased in CD226 knockout mice than that in control mice when both received EAE induction.
Blocking CD226 inhibited NK cell-mediated cytotoxicity of the GM-CSF (show CSF2 Antibodies)-stimulated Flt3 ligand (show FLT3LG Antibodies) conventional dendritic cells. The CD226(+)NKG2A (show KLRC1 Antibodies)(-) subset of NK cells was better at targeting GM-CSF (show CSF2 Antibodies)-stimulated Flt3 ligand (show FLT3LG Antibodies) conventional dendritic cells. CD155 (show PVR Antibodies), a known ligand for CD226, could also act as an inhibitor of NK cell-mediated lysis, as dendritic cells lacking CD155 (show PVR Antibodies) were more sensitive to NK cell-mediated lysis.
inflammatory monocytes, together with NK cells, are essential in the early control of CMV through the DNAM-1-PVR (show PVRL2 Antibodies) pathway.
Data show that CD155 (show PVR Antibodies) protein/CD226 antigen mainly mediates the interaction between NK cells and leukemic cells in acute myeloid leukemia (show BCL11A Antibodies). To investigate the interaction between leukemic cells
absence of either CD155 (show PVR Antibodies) or CD226 in BALB/c mice causes a profound shift in the Natural Killer T-Cells subtype composition in thymus, expanding the frequency and numbers of iNKT1 cells at the expense of iNKT2 cells, as well as iNKT17 cells.
our results suggest a limited role for DNAM-1 in solid allograft rejection. Blocking DNAM-1 is not sufficient to prevent allograft rejection and might be relevant only in combination with additional inhibitors of costimulation.
we propose that expression of DNAM-1 on inflammatory monocytes are evolutionally conserved and act as an adhesion molecule (show NCAM1 Antibodies) on blood inflammatory monocytes.
Data indicate that DNAM-1 (CD226) signaling was required to enhance cytotoxicity.
Regulatory T cells derived (show CD4 Antibodies)from Cd226-deficient mice showed similarly reduced inhibitory activity, eventually resulting in an exacerbated disease course of experimental autoimmune encephalomyelitis.
Natural killer cells and cytotoxic T cells express both TIGIT (show TIGIT Antibodies) and DNAM-1 receptors, and in certain cases their effector functions are dictated by TIGIT (show TIGIT Antibodies) or DNAM-1 signaling. Agonist and antagonist antibodies targeting either TIGIT (show TIGIT Antibodies) or DNAM-1 present many therapeutic options for diseases spanning from cancer to auto-immunity. (Review)
Results show that CD226 expression was down-regulated in human hepatocellular carcinoma (HCC (show FAM126A Antibodies)) cells. MiR (show MLXIP Antibodies)-892a directly targeted CD226 promoting HCC (show FAM126A Antibodies) cells proliferation and invasion.
cumulative incidences of acute graft-versus-host disease in patients with high maximal serum levels of sDNAM-1 (>/=30 pM) in the 7 days before allogeneic hematopoietic stem cell transplantation were significantly higher than those in patients with low maximal serum levels of sDNAM-1 in the same period. Our data suggest sDNAM-1 is potentially a unique candidate as a predictive biomarker for the development of acute GVHD.
Our results support an important association of rs4810485 in CD40 (show CD40 Antibodies) gene and rs763361 in CD226 gene polymorphism, combined effect of rs4810485 and rs763361 with increased risk of systemic lupus erythematosus.
our results support and explain the mechanism behind the recently reported finding that in EOC, NK-cell recognition and killing of tumor cells was mainly dependent on DNAM-1 signaling while the contribution of the NKG2D (show KLRK1 Antibodies) receptor-ligand pathway was complementary and uncertain.
CD226 rs763361 polymorphism was significantly associated with susceptibility to T1D.
Age and CMV serostatus influence the expression of NKp30 (show NCR3 Antibodies), NKp46 (show NCR1 Antibodies) and DNAM-1 activating receptors on resting and IL-2 (show IL2 Antibodies) activated natural killer cells.
DNAM-1 ligands CD112 (show PVRL2 Antibodies) and CD155 (show PVR Antibodies) as well as the NKG2D (show KLRK1 Antibodies) ligands MICA (show MICA Antibodies) and MICB (show MICB Antibodies) were expressed on the hiPSC lines
This gene encodes a glycoprotein expressed on the surface of NK cells, platelets, monocytes and a subset of T cells. It is a member of the Ig-superfamily containing 2 Ig-like domains of the V-set. The protein mediates cellular adhesion of platelets and megakaryocytic cells to vascular endothelial cells. The protein also plays a role in megakaryocytic cell maturation.
, CD226 molecule
, platelet and T cell activation antigen 1
, platelet and T-cell activation antigen 1
, DNAX accessory molecule 1
, DNAX accessory molecule-1
, T lineage-specific activation antigen 1 antigen
, adhesion glycoprotein