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SELPLG encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-, E- and L- selectin expressed on myeloid cells and stimulated T lymphocytes. Zusätzlich bieten wir Ihnen SELPLG Kits (32) und SELPLG Proteine (13) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 264 products:
Mouse (Murine) Monoclonal SELPLG Primary Antibody für BR, FACS - ABIN1177261
Borges, Eytner, Moll, Steegmaier, Campbell, Ley, Mossmann, Vestweber: The P-selectin glycoprotein ligand-1 is important for recruitment of neutrophils into inflamed mouse peritoneum. in Blood 1997
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Human Monoclonal SELPLG Primary Antibody für CyTOF, ELISA - ABIN262947
Walcheck, Leppanen, Cummings, Knibbs, Stoolman, Alexander, Mattila, McEver: The monoclonal antibody CHO-131 binds to a core 2 O-glycan terminated with sialyl-Lewis x, which is a functional glycan ligand for P-selectin. in Blood 2002
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Human Monoclonal SELPLG Primary Antibody für Func, FACS - ABIN610433
Connolly, Chait, Duncan, Taylor: CT-guided percutaneous needle biopsy of small lung nodules in children. in Pediatric radiology 1999
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Human Monoclonal SELPLG Primary Antibody für BR, FACS - ABIN967489
Snapp, Ding, Atkins, Warnke, Luscinskas, Kansas: A novel P-selectin glycoprotein ligand-1 monoclonal antibody recognizes an epitope within the tyrosine sulfate motif of human PSGL-1 and blocks recognition of both P- and L-selectin. in Blood 1998
Human Monoclonal SELPLG Primary Antibody für CyTOF, FACS - ABIN4348165
Wake, Mori, Liu, Morioka, Teshigawara, Sakaguchi, Kuroda, Gao, Takahashi, Ohtsuka, Yoshino, Morimatsu, Nishibori: Histidine-Rich Glycoprotein Prevents Septic Lethality through Regulation of Immunothrombosis and Inflammation. in EBioMedicine 2016
Results suggest that PSGL-1 may play an oncogenic role in the development of intestinal tumors, and this is likely mediated through activation of NFkB signaling by MIP (zeige TNPO1 Antikörper)-1g.
c-Myc (zeige MYC Antikörper) regulates P-selectin glycoprotein ligand-1 expression in monocytes during HIV-1 infection.
The percentage of CXCR3 (zeige CXCR3 Antikörper)(+) CD4 (zeige CD4 Antikörper)(+) TEM (zeige CYLD Antikörper) cells negatively correlated with the severity of the cutaneous disease in psoriasis patients. Importantly CLA(+) CD4 (zeige CD4 Antikörper)(+) TCM cells expressing CCR6 (zeige CCR6 Antikörper)(+) or CCR4 (zeige CCR4 Antikörper)(+)CXCR3 (zeige CXCR3 Antikörper)(+) negatively correlated with psoriasis severity suggesting recruitment to the skin compartment.
Platelet-leukocyte aggregations increased in acute ischemic stroke patients rapidly within 3h. The I allele of PSGL-1 M62I was associated with risk of developing acute ischemic stroke, especially large artery atherosclerosis stroke and small artery occlusion stroke. Small artery occlusion stroke patients with the II genotype of PSGL-1 M62I have the higher level of platelet-neutrophil aggregates.
The significant presence of CLA+ T cells and E-selectin (zeige SELE Antikörper) expressions in the OLPG suggests their involvement in the etiopathogenesis of OLP; however, only a weak correlation between CLA+ T cells and E-selectin (zeige SELE Antikörper) was observed.
PSGL-1 is a novel receptor for S. pneumoniae that contributes to protection against invasive pneumococcal disease.
This study provides a better understanding of the biology of P-selectin (zeige SELP Antikörper) and PSGL-1 and their roles in dissemination and resensitization of Multiple myeloma treatment.
Report influence of SELPLG variation on leukocyte-platelet interactions in cardiovascular disease.
E-selectin (zeige SELE Antikörper) interactions with glycoprotein ligands (CD44 (zeige CD44 Antikörper)/hematopoietic cell E-/L-selectin (zeige SELL Antikörper) ligand and PSGL-1) mediate the initial capturing of cells out of flow.
CD162 staining and the staining degree, with the other standard immunohistochemical stains, were shown to be beneficial in the diagnosis of multiple myeloma disease.
results indicate that P-selectin (zeige SELP Antikörper) deletion significantly decreases tumor stiffness in Rip1 (zeige RALBP1 Antikörper)-Tag2 mice by inhibiting LOX (zeige LOX Antikörper) expression.
this study shows that PSGL-1 plays a fundamental role in balancing viral control and immunopathology and also functions to regulate T cell responses in the tumor microenvironment
Psgl-1 deficiency accelerates bleomycin-induced lung fibrosis and inflammation in mice through activating the PI3K/AKT (zeige AKT1 Antikörper) axis.
Circulating soluble P-selectin (zeige SELP Antikörper) must dimerize to promote inflammation and thrombosis in mice.
The results from the present study suggest that activated platelets secrete Pselectin to promote cardiac inflammation and fibrosis in Ang (zeige ANG Antikörper) IIinduced hypertension.
These findings indicate a novel pathway in tumor metastasis, i.e., tumor cell mediated activation of P-selectin (zeige SELP Antikörper) in platelets, followed by activation and secretion of Asm (zeige SMPD1 Antikörper) and in turn release of ceramide and tumor metastasis. The data suggest that p38 MAPK (zeige MAPK14 Antikörper) acts downstream from P-selectin (zeige SELP Antikörper) and is necessary for the secretion of Asm (zeige SMPD1 Antikörper).
Psgl-1 deficiency is protective against the prothrombotic effects of IL-1beta (zeige IL1B Antikörper) .
PSGL-1, CD43, and CD44 moved normally to the uropods of chemokine-stimulated C1galt1(-/-) neutrophils
these results demonstrate that P-selectin (zeige SELP Antikörper) expression on ECs is regulated in part by glycosylation mechanisms and that glycosylation inhibitors efficiently reduce the adhesion of sRBCs and leukocytes to ECs.
endothelial colony-forming cells interact with activated neutrophils via PSGL-1 and L-selectin (zeige SELL Antikörper)
This gene encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-, E- and L- selectin expressed on myeloid cells and stimulated T lymphocytes. As such, this protein plays a critical role in leukocyte trafficking during inflammation by tethering of leukocytes to activated platelets or endothelia expressing selectins. This protein requires two post-translational modifications, tyrosine sulfation and the addition of the sialyl Lewis x tetrasaccharide (sLex) to its O-linked glycans, for its high-affinity binding activity. Aberrant expression of this gene and polymorphisms in this gene are associated with defects in the innate and adaptive immune response. Alternate splicing results in multiple transcript variants.
P-selectin glycoprotein ligand 1
, cutaneous lymphocyte-associated associated antigen
, selectin P ligand
, P-selectin glycoprotein ligand 1 propeptide
, P-selectin glycoprotein ligand-1
, leukocyte cell surface adhesion molecule
, selectin, platelet (p-selectin) ligand