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Human Polyclonal OBSCN Primary Antibody for ELISA, WB - ABIN529547
Hu, Kontrogianni-Konstantopoulos: The kinase domains of obscurin interact with intercellular adhesion proteins. in FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2013
OBSCN mutations may result in the development of a familial dilated cardiomyopathy (DCM) phenotype via haploinsufficiency. These mutations should be considered as a significant causal factor of DCM, alone or in concert with other mutations.
Gene-based association analyses shows nominal significant association with multifocal fibromuscular dysplasia for obscurin.
Loss of the obscurin-RhoGEF downregulates RhoA (show RHOA Antibodies) signaling and increases microtentacle formation and attachment of breast epithelial cells.
this study presents here the X-ray structure of the human titin:obscurin M10:O1 complex extending our previous work on the M10:OL1 interaction.
Obscurin and KCTD6 regulate cullin-dependent small ankyrin-1 (show ANK1 Antibodies) (sAnk1.5) protein turnover
OBSCN polymorphisms, in particular, highly conserved nonsynonymous Leu2116Phe variant, might contribute to aspirin hypersensitivity in asthmatics
Results describe the molecular basis for the head-to-tail interaction of the carboxyl terminus of titin and the amino-terminus of obscurin-like-1 by X-ray crystallography.
Results suggest that obscurin binds small ankyrin 1 (show ANK1 Antibodies), and document a specific and direct interaction between proteins of the sarcomere and the sarcoplasmic reticulum.
The complete gene giant muscle protein obscurin was analysed. The fusion of the conventional obscurin A, containing only the GEF (show SLC2A4RG Antibodies) domain, and obscurin B, fusing into the 3' kinase exons, was experimentally confirmed and analysed.
OBSCN and C9orf65 (show PRUNE2 Antibodies) comprise a highly accurate two-gene classifier for differentiating gastrointestinal stromal tumors and leiomyosarcomas.
Altogether, these results suggest that obscurin is required for the maintenance of morphological and ultrastructural integrity of skeletal muscle fibers against damage induced by intense mechanical stress and point to the diaphragm as the skeletal muscle most severely affected in obscurin-deficient mice.
obscurins are not restricted to striated (show NSDHL Antibodies) muscles, but are abundantly expressed in several tissues and organs including brain, skin, kidney, liver, spleen, and lung.
the obscurin kinase domains, SK1 (show SPHK1 Antibodies) and SK2 (show PAPSS2 Antibodies), are active enzymes with distinct substrate specificities.
Obscurin, by targeting ankB (show ANKH Antibodies) at the M band, contributes to the organization of subsarcolemma microtubules, localization of dystrophin (show DMD Antibodies) at costameres, and maintenance of sarcolemmal integrity.
Results support a role of obscurin in mediating the subcellular localization of small ankyrin1 isoforms in striated (show NSDHL Antibodies) muscle cells.
the Rho-GEF (show ARHGEF2 Antibodies) domain of obscurin interacts with RanBP9 (show RANBP9 Antibodies) and that both can interact with the N-terminal region of titin (show TTN Antibodies) to influence the formation of the Z-disk and A/I junction
ANK2 (show ANK2 Antibodies) is subject to alternative splicing that gives rise to unique polypeptides with diverse roles in cardiac function.
the organization of obscurin at different locations in the sarcomere changes during muscle development and that this might affect the interaction with ank1.5.
The obscurin gene spans more than 150 kb, contains over 80 exons and encodes a protein of approximately 720 kDa. The encoded protein contains 68 Ig domains, 2 fibronectin domains, 1 calcium/calmodulin-binding domain, 1 RhoGEF domain with an associated PH domain, and 2 serine-threonine kinase domains. This protein belongs to the family of giant sacromeric signaling proteins that includes titin and nebulin, and may have a role in the organization of myofibrils during assembly and may mediate interactions between the sarcoplasmic reticulum and myofibrils. Alternatively spliced transcript variants encoding different isoforms have been identified.
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
, obscurin, myosin light chain kinase
, obscurin-myosin light chain kinase