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Desmosomes are intercellular junctions that tightly link adjacent cells. De plus, nous expédions Desmoplakin Anticorps (49) et et beaucoup plus de produits pour cette protéine.
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Human Desmoplakin Kit ELISA pour 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. dans Molecular & cellular proteomics : MCP 2013
Our data suggest that endurance exercise accelerates arrhythmogenic ventricular cardiomyopathy pathogenesis in transgenic DSP mice
GSK3- and PRMT-1 (Montrer PRMT1 Kits ELISA)-dependent modifications of desmoplakin control desmoplakin-cytoskeleton dynamics.
These data indicate a function of desmoplakin in motor nerve regeneration by linking N-cadherin (Montrer CDH2 Kits ELISA) to intermediate filaments in regenerating motor axons.
A loss of desmoplakin expression led to an abnormal distribution of Cx43 (Montrer GJA1 Kits ELISA) and Nav1.5 (Montrer SCN5A Kits ELISA), 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 (Montrer FXR1 Kits ELISA) 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 (Montrer CDH1 Kits ELISA), than to the desmogleins.
Data show suppression of desmoplakin expression leads to nuclear localization of plakoglobin (Montrer JUP Kits ELISA) and a 2-fold reduction in canonical Wnt (Montrer WNT2 Kits ELISA)/beta-catenin (Montrer CTNNB1 Kits ELISA) signaling through Tcf (Montrer HNF4A Kits ELISA)/Lef1 (Montrer LEF1 Kits ELISA) transcription factors.
Novel desmoplakin frameshift deletion p.Thr2625fs (c.7871_7872delAC) was identified as a potential cause of heart disease and sudden cardiac death in a Polish family.
This is the first report of DSP genetic screening in Chinese sudden unexplained nocturnal death syndrome (SUNDS) and Brugada syndrome. Our results imply that DSP mutations contribute to the genetic cause of some SUNDS victims and maybe a new susceptible gene for Brugada syndrome.
Syndrome featuring erythrokeratodermia and cardiomyopathy (EKC (Montrer TAC4 Kits ELISA)) caused by mutation in DSP was described. Specific region of DSP protein critical to the pathobiology of EKC (Montrer TAC4 Kits ELISA) 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 (Montrer PKP2 Kits ELISA)/DSP mutations in patient with Brugada syndrome and ventricular tachycardia.
Patients whose MPM tissues expressed elevated mRNA levels of BIRC5 (Montrer BIRC5 Kits ELISA), DSP, NME2, and THBS2 (Montrer THBS2 Kits ELISA) 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 (Montrer MAPRE2 Kits ELISA) interactions and altering microtubule dynamics.
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