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Mammalian Monoclonal CNTNAP1 Primary Antibody für ISt, IHC - ABIN1304570
Xing, Röth, Stratton, Chuang, Danne, Ellis, Ng, Kilpatrick, Merson: Adult neural precursor cells from the subventricular zone contribute significantly to oligodendrocyte regeneration and remyelination. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2014
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Chicken Monoclonal CNTNAP1 Primary Antibody für IF, IP - ABIN967780
Brandt, Gimona, Hillmann, Haller, Mischak: Protein kinase C induces actin reorganization via a Src- and Rho-dependent pathway. in The Journal of biological chemistry 2002
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Chicken Monoclonal CNTNAP1 Primary Antibody für IF, IP - ABIN967781
Maddox, Burridge: RhoA is required for cortical retraction and rigidity during mitotic cell rounding. in The Journal of cell biology 2003
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In two brothers with severe congenital hypotonia and foot deformities, we identified compound heterozygous variants in CNTNAP1, reporting the first causative missense variant, p.(Cys323Arg). Motor nerve conductions were markedly decreased.
CNTNAP1 mutations were found to induce characteristic ultrastructural lesions of the paranodal region.
report a consanguineous Arab family from Qatar with three children having an early lethal form of arthrogryposis multiplex congenita and a novel frameshift mutation in CNTNAP1
Mutations in CNTNAP1 and ADCY6 (zeige ADCY6 Antikörper) are responsible for severe arthrogryposis multiplex congenita with axoglial defects
VDAC1 (zeige VDAC1 Antikörper) and CNTNAP1 associate with gamma-secretase in detergent-resistant membranes and affect amyloid precursor protein (zeige APP Antikörper) processing.
Simultaneous deletion of Caspr and Caspr2 (zeige CNTNAP2 Antikörper) disrupts the internodal organization of Kv1.2 (zeige KCNA2 Antikörper).
Caspr co-localizes and interacts with APP (zeige APP Antikörper). Amyloid-beta (Abeta (zeige APP Antikörper)) 40 and Abeta42 generation were also reduced in HEK (zeige EPHA3 Antikörper)-APP (zeige APP Antikörper) cells by Caspr overexpression.
Caspr labeling was observed through much of the retina, including horizontal, bipolar, amacrine, and ganglion cells.
Clustering of Caspr at initial contact sites between OL processes and the axon requires glial expression of NF155 but not of contactin. Expression of membrane proteins along the axolemma is determined by the type of the contacting glial cells.
These results suggest that Caspr serves as a "transmembrane scaffold" that stabilizes the Caspr/contactin adhesion complex at the paranodal junction by connecting it to cytoskeletal components within the axon.
F3/contactin and caspr/paranodin traffic to the cell surface via a non-conventional pathway
Nogo-A (zeige RTN4 Antikörper) interacts in trans with axonal Caspr at CNS paranodes, an interaction that may have a role in modulating axon-glial junction architecture and possibly K(+)-channel (zeige KCNC4 Antikörper) localization during development.
the Caspr/Cont complex is essential for the formation of axoglial SJ
Caspr protein is required for recruitment and retention of KCNQ4 (zeige KCNQ4 Antikörper) at calyceal synapses in vestibular hair cells.
The Caspr gene has been identified in the neurological mutant shambling (shm) mouse and shown to encode the contactin-associated protein, which is a major component of the paranodal junction in myelinated nerves.
The gene product was initially identified as a 190-kD protein associated with the contactin-PTPRZ1 complex. The 1,384-amino acid protein, also designated p190 or CASPR for 'contactin-associated protein,' includes an extracellular domain with several putative protein-protein interaction domains, a putative transmembrane domain, and a 74-amino acid cytoplasmic domain. Northern blot analysis showed that the gene is transcribed predominantly in brain as a transcript of 6.2 kb, with weak expression in several other tissues tested. The architecture of its extracellular domain is similar to that of neurexins, and this protein may be the signaling subunit of contactin, enabling recruitment and activation of intracellular signaling pathways in neurons.
contactin associated protein 1
, contactin-associated protein 1-like
, contactin-associated protein 1
, neurexin 4
, neurexin IV
, neurexin 4 (contactin associated protein)