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ICAM1 encodes a cell surface glycoprotein which is typically expressed on endothelial cells and cells of the immune system. Additionally we are shipping ICAM-1 Antibodies (784) and ICAM-1 Kits (150) and many more products for this protein.
Showing 10 out of 59 products:
Mouse (Murine) ICAM-1 Protein expressed in CHO Cells - ABIN2666825
Greve, Davis, Meyer, Forte, Yost, Marlor, Kamarck, McClelland: The major human rhinovirus receptor is ICAM-1. in Cell 1989
Show all 8 references for ABIN2666825
Human ICAM-1 Protein expressed in CHO Cells - ABIN2666823
Rothlein, Dustin, Marlin, Springer: A human intercellular adhesion molecule (ICAM-1) distinct from LFA-1. in Journal of immunology (Baltimore, Md. : 1950) 1986
Show all 8 references for ABIN2666823
Human ICAM-1 Protein expressed in Escherichia coli (E. coli) - ABIN1047208
Staunton, Marlin, Stratowa, Dustin, Springer: Primary structure of ICAM-1 demonstrates interaction between members of the immunoglobulin and integrin supergene families. in Cell 1988
Show all 3 references for ABIN1047208
Human ICAM-1 Protein expressed in Human Cells - ABIN2002637
Bhalla, Chugh, Mehrotra, Rathore, Tousif, Prakash Dwivedi, Prakash, Kumar Samuchiwal, Kumar, Kumar Singh, Ghanwat, Kumar, Das, Mohmmed, Malhotra, Ranganathan: Host ICAMs play a role in cell invasion by Mycobacterium tuberculosis and Plasmodium falciparum. in Nature communications 2015
Our results also supported the hypothesis that the KK genotype at the K469E locus in ICAM-1 is a risk factor for AIS (show AR Proteins).
genetic association study in Malaysian population: Data suggest that an SNP in ICAM1 [rs5498, K469E(A/G)] is associated with diabetic nephropathy (DN) in subjects with type 2 diabetes in the population studied; plasma ICAM1 is up-regulated in DN.
The effect of IL-35 on electrical impedance reflecting tissue integrity, the surface expression of ICAM-1 and mRNA expression of IL-32 (show IL32 Proteins), as well as apoptosis in human primary aortic smooth muscle cells (Ao-SMCs) was investigated
ABL (show ABL1 Proteins)-N administration induced apoptosis of PC3 (show PCSK1 Proteins) cells in a dose-dependent manner, along with the enhanced activity of caspases and increased Bax (show BAX Proteins)/Bcl-2 (show BCL2 Proteins) ratio. Expression of KLF5 (show KLF5 Proteins), Stat5b (show STAT5B Proteins) and ICAM-1 was significantly downregulated in PC3 (show PCSK1 Proteins) cells.
Contact-dependent lung adenocarcinoma aggregate dispersion by M2a macrophages occurs via ICAM-1 and beta2 integrin interactions.
Lipopolysaccharides up-regulate ICAM-1 expression in breast cancer cells via a MyD88 (show MYD88 Proteins)-BLT2-ERK (show EPHB2 Proteins)-linked signaling cascade.
The genotypic distributions of ICAM-1 (K469E) were significantly different between patients and controls.
ICAM1 and CD44 (show CD44 Proteins) could have a compensation effect on maintaining the stemness characteristics of esophageal squamous cell carcinoma.
expression levels of ICAM-1, NF-kappaB (show NFKB1 Proteins), and MCP-1 (show CCL2 Proteins) in patients are significantly elevated, suggesting an enhanced chronic inflammatory response and a significant correlation between inflammatory factors and the pathogenesis of cerebral aneurysm
Identify the selectins ICAM-1 and VCAM-1 (show VCAM1 Proteins) as strong and independent predictors of all-cause and cardiovascular mortality in patients with stable carotid atherosclerosis.
Luteolin may inhibit tumor angiogenesis and tumor cell proliferation by down-regulation of LFA- 3 and PCNA (show PCNA Proteins) and up-regulation of ICAM-1 in tumor tissue of tumor-bearing mice, thereby achieving its anti-tumor effect.
our results further highlight the pleiotropic role of ICAM-1 in T-cell-dependent immune responses, with a major role in Treg cell development and suppressive function.
the present results shed light on regulation of expression and function of ICAM-1 on neutrophils and identify it as an additional regulator of neutrophil effector responses in host defense.
we identified intracellular adhesion molecule (ICAM)-1, through fibrinogen binding, as a previously unreported mediator of platelet-monocyte interactions
miR (show MLXIP Proteins)-222 was transported into recipient endothelial cells by endothelial microparticles and functionally regulated expression of its target protein ICAM-1 in vitro and in vivo.
Timely blockade of ICAM-1.LFA-1 (show ITGAL Proteins) interaction prevents disease onset in a mouse model of emphysema.
MRTF-A/B depletion results in an increase in the cell surface expression of ICAM-1 and interactions between HAoECs and leukocytes
neutrophils are reliant on endothelial activation for adhesion, initially via E-selectin (show SELE Proteins) and subsequently, by integrin-mediated binding to ICAM-1 and VCAM-1 (show VCAM1 Proteins), combined with CXCL8 (show IL8 Proteins)-dependent chemotaxis.
Inhibition of the P2RX7 (show P2RX7 Proteins) pathway not only decreased endothelial ICAM-1 expression and leukocyte adhesion but also prevented microglia overactivation, reduced brain injury, and consequently doubled the early survival of septic mice.
ICAM-1 in the tumor microenvironment, via restraining efferocytosis of apoptotic tumor cells, can block M2 macrophage polarization through regulation of PI3K/AKT (show AKT1 Proteins) activation, which leads to prevention of tumor metastasis.
ADMA has potent adverse effects on cell proliferation, intracellular ROS (show ROS1 Proteins) generation, cell permeability, levels of ICAM-1, and the tight-junction protein occludin (show OCLN Proteins)
Neutrophil lung infiltrations in porcine reproductive and respiratory syndrome virus infection infected animals is both ICAM-1 dependent and independent.
Chitosan oligosaccharides downregulate the expression of E-selectin (show SELE Proteins) and ICAM-1 by inhibiting the phosphorylation of Mitogen-Activated Protein Kinases and the activation of NF-kappaB (show NFKB1 Proteins) in lipopolysaccharides treated porcine iliac artery endothelial cells.
Data show that all five molecules, BNP, ICAM-1, TNF-alpha (show TNF Proteins), VCAM-1 (show VCAM1 Proteins) and IL-6 (show IL6 Proteins), quickly and reliably signaled adverse interactions.
Altered shear stress stimulates upregulation of endothelial VCAM-1 (show VCAM1 Proteins) and ICAM-1 in a BMP-4 (show BMP4 Proteins)- and TGF-beta1 (show TGFB1 Proteins)-dependent pathway.
ICAM1 and IL10 (show IL10 Proteins) were upregulated in ventilator-induced lung injury. Nuclear transcription factor AP-1 (show JUN Proteins) may be responsible for this upregulation.
Hepatocellular glycogen (show GYS1 Proteins) decreases the expression of ICAM-1 mRNA of hepatic stellate cells.
This gene encodes a cell surface glycoprotein which is typically expressed on endothelial cells and cells of the immune system. It binds to integrins of type CD11a / CD18, or CD11b / CD18 and is also exploited by Rhinovirus as a receptor.
intercellular adhesion molecule 1
, intercellular adhesion molecule 1-like
, cell surface glycoprotein P3.58
, intercellular adhesion molecule 1 (CD54), human rhinovirus receptor
, major group rhinovirus receptor
, leukocyte adhesion molecule