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Human Polyclonal CLDN18 Primary Antibody for IHC, IHC (p) - ABIN4892664
Jun, Kim, Jung, Choi, Chin: Expression of claudin-7 and loss of claudin-18 correlate with poor prognosis in gastric cancer. in International journal of surgery (London, England) 2014
Show all 2 Pubmed References
CDH17 and CLDN18 are useful target molecules. Their coupling can aid in the comprehensive detection and localization of gastric cancer metastases in vivo to overcome challenges associated with intratumoral heterogeneity.
Bile duct adenocarcinoma cells overexpress claudin-18 via the EGFR (show EGFR Antibodies)/RAS/ERK (show EPHB2 Antibodies) pathway, contributing to cell proliferation and invasion.
The presented data substantiate the hypothesis that claudin-18 is a central barrier-forming component of tight junctions and show that IL-13 (show IL13 Antibodies) downregulates claudin-18. These data also suggest that the loss of claudin-18 is associated with increased sensitization to aeroantigens and airway responsiveness
suggest that the reduction of CLDN5 (show CLDN5 Antibodies), 7, and 18 expression loses the suppressive ability of interaction between PDK1 (show PDK1 Antibodies) and Akt (show AKT1 Antibodies) and causes sustained phosphorylation of Akt (show AKT1 Antibodies), resulting in the disordered proliferation in lung squamous carcinoma cells
Data suggest that claudin-18 suppresses the abnormal proliferation and motility of lung epithelial cells mediated by inhibition of phosphorylation of pyruvate dehydrogenase kinase isoform 1 (PDK1 (show PDK1 Antibodies)) and proto-oncogene (show RAB1A Antibodies) protein c (show PROC Antibodies)-akt (Akt (show AKT1 Antibodies)).
Human fetal lungs at 23-24 weeks gestational age, the highest-risk period for developing bronchopulmonary dysplasia, a disease of impaired alveolarization, had significantly lower CLDN18 expression relative to postnatal lungs.
Evaluated expression of claudins in gastric cancer and determined their significance for patient outcome. Claudin-3 (show CLDN3 Antibodies) and claudin-7 (show CLDN7 Antibodies) were expressed in 25.4% and 29.9% of gastric cancer tissues; 51.5% of gastric cancer tissues had reduced claudin-18.
High levels of CLDN18 are associated with non-small-cell lung cancer.
Downregulation of miR (show MLXIP Antibodies)-1303 can inhibit proliferation, migration and invasion of gastric cancer cells by targeting CLDN18.
Claudin-18 positivity is a specific phenotype that is characteristic of intestinal-type Mucinous borderline tumours of the ovary
The claudin-18 knockout mice exhibited decreased P2X7 (show P2RX7 Antibodies) mRNA transcript abundance as measured by mRNA expression microarray
CLDN18 deficiency results in epithelial barrier dysfunction, injury, and impaired alveolarization in mice.
Identify a role for claudin 18 in alveolar fluid homeostasis beyond its direct contributions to barrier properties.
we conclude that the estrogen effects on osteoclasts may in part be mediated via regulation of Cldn-18 signaling
Claudin-18 is expressed at the variety of epithelial tissues in inner ear including Organ of Corti, stria vascularis, Reissner's membrane, spiral limbus, vestibular sensory epithelia, and dark cell area.
Cldn-18 is a novel negative regulator of bone resorption and osteoclast differentiation
Claudin-18 forms a paracellular barrier against H(+) in the stomach. Deficiency causes paracellular H(+) leak, up-regulation of proinflammatory cytokines, recruitment of neutrophils, and atrophic gastritis.
Increased expression of claudin-18 is associated with ulcerative colitis.
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is upregulated in patients with ulcerative colitis and highly overexpressed in infiltrating ductal adenocarcinomas. PKC/MAPK/AP-1 (protein kinase C/mitogen-activated protein kinase/activator protein-1) dependent pathway regulates the expression of this gene in gastric cells. Alternatively spliced transcript variants encoding different isoforms have been identified.
, surfactant associated 5
, surfactant associated protein J
, surfactant, pulmonary associated protein J
, claudin 18-like