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Desmosomes are intercellular junctions that tightly link adjacent cells. Additionally we are shipping Desmoplakin Antibodies (43) and many more products for this protein.
Showing 10 out of 28 products:
Human Desmoplakin ELISA Kit for Sandwich ELISA - ABIN415286
Kosanam, Prassas, Chrystoja, Soleas, Chan, Dimitromanolakis, Blasutig, Rückert, Gruetzmann, Pilarsky, Maekawa, Brand, Diamandis: Laminin, gamma 2 (LAMC2): a promising new putative pancreatic cancer biomarker identified by proteomic analysis of pancreatic adenocarcinoma tissues. in Molecular & cellular proteomics : MCP 2013
Our data suggest that endurance exercise accelerates arrhythmogenic ventricular cardiomyopathy pathogenesis in transgenic DSP mice
GSK3- and PRMT-1 (show PRMT1 ELISA Kits)-dependent modifications of desmoplakin control desmoplakin-cytoskeleton dynamics.
These data indicate a function of desmoplakin in motor nerve regeneration by linking N-cadherin (show CDH2 ELISA Kits) to intermediate filaments in regenerating motor axons.
A loss of desmoplakin expression led to an abnormal distribution of Cx43 (show GJA1 ELISA Kits) and Nav1.5 (show SCN5A ELISA Kits), while scrapeloading dye/transfer revealed a decrease in dye transfer in DSP siRNAtreated cells.
the desmosomal protein desmoplakin is not essential for cell adhesion in the intestinal epithelium.
Fxr1 (show FXR1 ELISA Kits) knockout hearts exhibit an up-regulation of desmoplakin and talin2 proteins, which is accompanied by severe disruption of desmosome as well as costamere architecture and composition in the heart
Loss of desmoplakin expression and resultant disruption of desmosomal adhesion can promote increased local tumor invasion independent of adherens junction status.
desmoplakin has a role in capillary formation
desmocollins show a higher degree of similarity to the classical cadherins, such as E-cadherin (show CDH1 ELISA Kits), than to the desmogleins.
Data show suppression of desmoplakin expression leads to nuclear localization of plakoglobin (show JUP ELISA Kits) and a 2-fold reduction in canonical Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling through Tcf (show HNF4A ELISA Kits)/Lef1 (show LEF1 ELISA Kits) transcription factors.
Syndrome featuring erythrokeratodermia and cardiomyopathy (EKC (show TAC4 ELISA Kits)) caused by mutation in DSP was described. Specific region of DSP protein critical to the pathobiology of EKC (show TAC4 ELISA Kits) syndrome and to DSP function in the heart and skin was identified.
There is higher incidence of Myocarditis in DSP mutation carriers affected by Arrhythmogenic right ventricular dysplasia.
Case Reports: desmoplakin mutations associated with variable woolly hair or hypotrichosis, palmoplantar keratoderma, and cardiac manifestations.
Genetic testing revealed a novel combination of two heterozygous mutations in the DSP gene encoding desmoplakin
Case Report: PKP2 (show PKP2 ELISA Kits)/DSP mutations in patient with Brugada syndrome and ventricular tachycardia.
Patients whose MPM tissues expressed elevated mRNA levels of BIRC5 (show BIRC5 ELISA Kits), DSP, NME2, and THBS2 (show THBS2 ELISA Kits) showed a statistically significant shorter overall survival.
a subset of arrhythmogenic cardiomyopathy mutations, in addition to a mutation associated with skin fragility/woolly hair syndrome, impair gap junction localization and function by misregulating DP-EB1 (show MAPRE2 ELISA Kits) interactions and altering microtubule dynamics.
Arrhythmogenic right ventricular cardiomyopathy patients of a three-generation Spanish family with a novel nonsense genetic variation in the DSP gene.
The cardiomyopathy mechanisms varied accordingly to the specific types of DSP mutation identified and included haploinsufficiency, dominant-negative effects, or a combination hereof.
Desmosomes are intercellular junctions that tightly link adjacent cells. Desmoplakin is an obligate component of functional desmosomes that anchors intermediate filaments to desmosomal plaques. The N-terminus of desmoplakin is required for localization to the desmosome and interacts with the N-terminal region of plakophilin 1 and plakoglobin. The C-terminus of desmoplakin binds with intermediate filaments. In the mid-region of desmoplakin, a coiled-coiled rod domain is responsible for homodimerization. Mutations in this gene are the cause of several cardiomyopathies and keratodermas as well as the autoimmune disease paraneoplastic pemphigus.
, putative desmoplakin
, ORF112 DESMOPLAKIN
, 250/210 kDa paraneoplastic pemphigus antigen
, desmoplakin I
, desmoplakin II
, desmoplakin I/II
, desmosomal cytoskeletal connector molecule
, desmoplakin-related protein