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抗Mouse (Murine) Desmoplakin 抗体:
抗Human Desmoplakin 抗体:
抗Rat (Rattus) Desmoplakin 抗体:
Cow (Bovine) Monoclonal Desmoplakin Primary Antibody for IHC (fro), IF - ABIN452374
Giménez-Abián, Clarke, Giménez-Martín, Weingartner, Giménez-Abián, Carballo, Díaz de la Espina, Bögre, De la Torre: DNA catenations that link sister chromatids until the onset of anaphase are maintained by a checkpoint mechanism. in European journal of cell biology 2002
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Amphibian Monoclonal Desmoplakin Primary Antibody for IHC (fro), IF - ABIN111818
Cowin, Kapprell, Franke: The complement of desmosomal plaque proteins in different cell types. in The Journal of cell biology 1985
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Chicken Monoclonal Desmoplakin Primary Antibody for IHC (fro), IHC (p) - ABIN112137
Moll, Moll: Comparative cytokeratin analysis of sweat gland ducts and eccrine poromas. in Archives of dermatological research 1991
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Chicken Monoclonal Desmoplakin Primary Antibody for IHC (fro), IF - ABIN452379
Franke, Schumacher, Borrmann, Grund, Winter-Simanowski, Schlechter, Pieperhoff, Hofmann: The area composita of adhering junctions connecting heart muscle cells of vertebrates - III: assembly and disintegration of intercalated disks in rat cardiomyocytes growing in culture. in European journal of cell biology 2007
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Cow (Bovine) Polyclonal Desmoplakin Primary Antibody for IHC (fro), IHC (p) - ABIN113449
Akat, Mennel, Kremer, Gassler, Bleck, Kartenbeck: Molecular characterization of desmosomes in meningiomas and arachnoidal tissue. in Acta neuropathologica 2003
Show all 2 references for ABIN113449
Human Polyclonal Desmoplakin Primary Antibody for ELISA, IHC - ABIN4305054
Barahona-Dussault, Benito, Campuzano, Iglesias, Leung, Robb, Talajic, Brugada: Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia. in Clinical genetics 2010
Conditional heterozygous deletion of Dsp in mice led to increased fibroadipogenesis in the heart and mild cardiac dysfunction.
Our data suggest that endurance exercise accelerates arrhythmogenic ventricular cardiomyopathy pathogenesis in transgenic DSP mice
GSK3 (显示 GSK3b 抗体)- and PRMT-1 (显示 PRMT1 抗体)-dependent modifications of desmoplakin control desmoplakin-cytoskeleton dynamics.
These data indicate a function of desmoplakin in motor nerve regeneration by linking N-cadherin (显示 CDH2 抗体) to intermediate filaments in regenerating motor axons.
A loss of desmoplakin expression led to an abnormal distribution of Cx43 (显示 GJA1 抗体) and Nav1.5 (显示 SCN5A 抗体), 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 (显示 FXR1 抗体) 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 (显示 CDH1 抗体), than to the desmogleins.
DSP is a desmosomal protein critical to cell-cell adhesion in a variety of cell types and important in wound healing and epithelial barrier function.
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 (显示 TAC4 抗体)) caused by mutation in DSP was described. Specific region of DSP protein critical to the pathobiology of EKC (显示 TAC4 抗体) 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 (显示 PKP2 抗体)/DSP mutations in patient with Brugada syndrome and ventricular tachycardia.
Patients whose MPM tissues expressed elevated mRNA levels of BIRC5 (显示 BIRC5 抗体), DSP, NME2, and THBS2 (显示 THBS2 抗体) showed a statistically significant shorter overall survival.
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