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CEP120 encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. De plus, nous expédions CEP120 Anticorps (20) et et beaucoup plus de produits pour cette protéine.
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The loss of Talpid3-binding centrosomal protein Cep120 results in failed centriole duplication and consequently ciliogenesis, which together underlie Cep120 mutant cerebellar hypoplasia.
Cep120 is required for centriole assembly and that the observed defect in neuronal migration might derive from a defect in this process.
The CEP120-associated phenotype ranges from mild classical JS in four patients to more severe conditions in two fetuses.
We establish a novel locus for Jeune asphyxiating thoracic dystrophy on 5q23.2 by linkage analysis and demonstrate that a mutation in CEP120 within this locus is the most likely cause of the disease.
CEP120 associates with SPICE1 (Montrer SPICE1 Kits ELISA) and CPAP (Montrer CENPJ Kits ELISA), and depletion of any of these proteins results in short procentrioles. Furthermore, CEP120 or CPAP (Montrer CENPJ Kits ELISA) overexpression results in excessive centriole elongation, a process dependent on CEP120, SPICE1 (Montrer SPICE1 Kits ELISA), and CPAP (Montrer CENPJ Kits ELISA).
CEP120 is a CPAP (Montrer CENPJ Kits ELISA)-interacting protein that positively regulates centriole elongation.
This gene encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. A similar protein in mouse plays a role in both interkinetic nuclear migration, which is a characteristic pattern of nuclear movement in neural progenitors, and in neural progenitor self-renewal. Mutations in this gene are predicted to result in neurogenic defects. Alternative splicing results in multiple transcript variants.
centrosomal protein of 120 kDa
, coiled-coil domain containing 100
, coiled-coil domain-containing protein 100