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Human Desmoglein 2 ELISA Kit for Sandwich ELISA - ABIN417921
Pillai, Sankoorikal, Johnson, Seneviratne, Zurko, Brown, Hathout, Rose: Directional secretomes reflect polarity-specific functions in an in vitro model of human bronchial epithelium. in American journal of respiratory cell and molecular biology 2014
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DSG2 as a key regulator of vasculogenic mimicry (VM) activity in human melanoma and suggest this molecule might be therapeutically targeted to reduce tumor blood supply and metastatic spread.
Data suggest that Dsg2 stimulates cell growth and migration by positively regulating EGFR (show EGFR ELISA Kits) level and signaling through a c-Src (show SRC ELISA Kits) and Cav1 (show CAV1 ELISA Kits)-dependent mechanism using lipid rafts as signal modulatory platforms.
identified DSG2 expression in distinct progenitor cell subpopulations and show that, independent from its classical functi (show HBA1 ELISA Kits)on as a component of desmosomes, this cadherin also plays a critical role in the vasculature
Data show that fetal pMSCs (mesenchymal stromal cells) expressing the highest levels of desmoglein 2, desmocollin 3 (show DSC2 ELISA Kits) and plakophilin 2 (show PKP2 ELISA Kits), followed by maternal pMSCs, while bmMSCs expressed the lowest levels.
Expression of the desmosomal protein Desmoglein-2 was reduced in pediatric dilated cardiomyopathy pediatric patients.
This study defines a mechanism by which Dsg2 expression in cancer cells can modulate the tumor microenvironment, a step critical for tumor progression.
Silencing of Dsg2 but not Dsc2 (show DSC2 ELISA Kits) resulted in loss of cell cohesion and enhanced migration, and invasion of pancreatic adenocarcinoma cells.
The homozygous desmoglein 2 variant c.1003A;G co-segregated with Arrhythmogenic right ventricular cardiomyopathy, indicating autosomal recessive inheritance and complete penetrance.
these data suggest that palmitoylation of Dsg2 regulates protein transport to the plasma membrane. Modulation of the palmitoylation status of desmosomal cadherins can affect desmosome dynamics.
Both Dsg2 mRNA and protein were highly expressed in non-small cell lung cancer (NSCLC) tissues and associated with NSCLC size, but not with overall survival of patients.
generated a Dsg2 loss-of-function strain (Dsg2 (lo/lo)) and observed that, in response to reduced levels of Dsg2: (i) CD31 (show PECAM1 ELISA Kits)(+) endothelial cells in the pancreas are hypertrophic and exhibit altered morphology, (ii) bone marrow-derived endothelial colony formation is impaired, (iii) ex vivo vascular sprouting from aortic rings is reduced, and (iv) vessel formation in vitro and in vivo is attenuated
Data suggest that loss of desmoglein 2 (Dsg2) compromises adhesion, and that this is a major pathogenic mechanism in DSG2-related and probably other desmosome-related arrhythmogenic cardiomyopathy (AC).
Dsg2 modulates Gli1 (show GLI1 ELISA Kits) expression. Dsg2-mediated hyperproliferation, MEK (show MDK ELISA Kits)/Erk1/2 (show MAPK1/3 ELISA Kits) activation, and accelerated squamous tumor development are enhanced on the Ptc1 (show PTCH1 ELISA Kits)+/lacZ (show GLB1 ELISA Kits) background.
a novel pathway of CSTA (show CSTA ELISA Kits) regulation involving Dsg2
Data demonstrate that desmoglein-2 plays a critical role in cardiomyocyte cohesion and function.
Data demonstrate that partner desmosomal cadherins Dsg2 and Dsc2 (show DSC2 ELISA Kits) play opposing roles in controlling colonic carcinoma cell proliferation through differential effects on EGFR (show EGFR ELISA Kits) signaling.
Dsg2 compensates for Dsg3 (show DSG3 ELISA Kits) depletion with regard to cell cohesion, but does not regulate p38 MAPK (show MAPK14 ELISA Kits) signaling.
In vivo interaction between Dsg2 and Na(V)1.5 provides a molecular pathway for the observed electrical disturbances during the early arrhythmogenic right ventricular cardiomyopathy.
Mutant desmoglein 2 cannot support the increased requirements placed on intercalated disc adhesion during postnatal heart development. This induces cardiomyocyte death, aseptic inflammation and fibrotic replacement.
ventricular arrhythmias that has been linked to mutations in desmosomal proteins including desmoglein 2
Desmosomes are cell-cell junctions between epithelial, myocardial, and certain other cell types. This gene product is a calcium-binding transmembrane glycoprotein component of desmosomes in vertebrate epithelial cells. Currently, three desmoglein subfamily members have been identified and all are members of the cadherin cell adhesion molecule superfamily. These desmoglein gene family members are located in a cluster on chromosome 18. This second family member is expressed in colon, colon carcinoma, and other simple and stratified epithelial-derived cell lines. Mutations in this gene have been associated with arrhythmogenic right ventricular dysplasia, familial, 10.
, Dsg alpha
, desmocollin a
, cadherin family member 5