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The protein encoded by ICAM2 is a member of the intercellular adhesion molecule (ICAM) family. Additionally we are shipping ICAM2 Antibodies (292) and ICAM2 Kits (45) and many more products for this protein.
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Data show that intercellular adhesion molecule 1 (ICAM-1 (show ICAM1 Proteins)) and ICAM-2 on B cells are essential for long-lasting cognate T follicular helper (Tfh)-B cell interactions and efficient selection of low-affinity B cell clones for proliferative clonal expansion.
These results indicate that, whereas T cells use ICAM-1 (show ICAM1 Proteins) and -2 for temporary pulmonary entrapment, neutrophils get sequestered and extravasate into inflamed lungs independent of ICAMs.
Results indicate that the interaction of ICAM-2 with alpha-actinin (show ACTN1 Proteins) is critical to conferring an ICAM-2-mediated non-metastatic phenotype in neuroblastoma (show ARHGEF16 Proteins) cells.
ICAM-2 regulates endothelial barrier function and permeability through a pathway involving N-Cadherin, ERMs and Rac-1
These findings highlight novel roles for ICAM-2 in mediating luminal neutrophil crawling and the effect on subsequent levels of extravasation.
beta2 integrin-mediated neutrophil crawling on endothelial ICAM-1 and ICAM-2 is a prerequisite for transcellular neutrophil diapedesis across the inflamed BBB.
a sequential involvement of endothelial ICAM-1 and VCAM-1 in mediating shear-resistant T cell arrest, followed by endothelial ICAM-1 and ICAM-2 in mediating T cell crawling to sites permissive for diapedesis across BBB endothelium.
unique role for ICAM-1 (show ICAM1 Proteins) in intraluminal lymphocyte crawling but redundant roles for ICAM-1 (show ICAM1 Proteins) and ICAM-2 in lymphocyte diapedesis and interstitial motility
show that the sequential expression of CD40 (show CD40 Proteins) and Icam2 delineate a transition in the acquisition of the blood potential from hemangioblast to hemogenic endothelium leading to the formation of primitive and definitive hematopoietic progenitors.
Data report the crystal structure of the radixin (show RDX Proteins) FERM (4.1 and ERM (show ETV5 Proteins)) domain complexed with the intercellular adhesion molecule-2 (ICAM-2) cytoplasmic peptide.
ICAM2 induction by p53 (show TP53 Proteins) has a key role in inhibiting cancer cell migration and invasion.ICAM2 acts at least in part through the suppression of the MEK (show MAP2K1 Proteins)-ERK (show EPHB2 Proteins) signaling pathway.
INDEED also identified some candidates previously reported to be relevant to HCC (show FAM126A Proteins), such as intercellular adhesion molecule 2 (ICAM2) and c4b-binding protein alpha chain (C4BPA (show C4BPA Proteins)), which were missed by both Differential expression and differential network analyses
Both ICAM-2 and ICAM-1 (show ICAM1 Proteins) levels in plasma were markedly increased in Ankylosing Spondylitis Chinese patients compared to controls.
Soluble ICAM2 was higher in ADHD patients than in controls.
ICAM-1 (show ICAM1 Proteins) and ICAM-2 are involved in each step of neutrophil extravasation, and have redundant but also distinct functions. Analysis of the role of endothelial ICAM-1 (show ICAM1 Proteins) requires simultaneous consideration of ICAM-2.
with larger patient groups and preferably detailed histopathological and clinical evaluations, are needed to explain the severity of ICAM-1 (show ICAM1 Proteins), ICAM-2, and ICAM-3 (show ICAM3 Proteins) molecules in Barrett's esophagus
ICAM-2 was significantly more pronounced in plasma cell mastitis than in nonpathologic breast tissue. However, no significant differences in ICAM-2 immunoreactivity were detected between ductal epithelium of PCM (show PCMT1 Proteins) and non-PCM (show PCMT1 Proteins).
Reduced glycosylation of ICAM-2 significantly attenuated, but did not abolish, its ability to suppress metastatic properties of neuroblastoma (show ARHGEF16 Proteins) cells.
These findings suggested that the downregulated miR (show MLXIP Proteins)-125b expression was associated with proliferation and radioresistance mechanisms, probably through ICAM2 signalling.
ICAM-2 plays a role in the cellular interactions associated with xenograft rejection
pig and human ICAM-2 promoters exhibit many similarities
The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein may play a role in lymphocyte recirculation by blocking LFA-1-dependent cell adhesion. It mediates adhesive interactions important for antigen-specific immune response, NK-cell mediated clearance, lymphocyte recirculation, and other cellular interactions important for immune response and surveillance. Several transcript variants encoding the same protein have been found for this gene.
intercellular adhesion molecule 2
, lymphocyte function-associated AG-1 counter-receptor