Nicastrin est un gène codé par le symbole NCSTN. Communément appelé aussi: NCSTN; KIAA0253. Nicastrin a une masse de 78.41kDa, une longueur d'acide aminé de 709, et est impliqué dans Acne inversa, familial, 1.
Nous proposons 6 des anticorps contre Nicastrin, élevé dans Lapin, qui sont appropriés pour le WB, IHC et ICC/IF avec des échantillons dérivés de Humain, Souris et Rat.
Informations sur les Gènes et les Protéines
Résumé UniProt
Essential subunit of the gamma-secretase complex, an endoprotease complex that catalyzes the intramembrane cleavage of integral membrane proteins such as Notch receptors and APP (amyloid-beta precursor protein) (PubMed:10993067, PubMed:12679784, PubMed:25043039, PubMed:26280335, PubMed:30598546, PubMed:30630874). The gamma-secretase complex plays a role in Notch and Wnt signaling cascades and regulation of downstream processes via its role in processing key regulatory proteins, and by regulating cytosolic CTNNB1 levels.
Résumé Entrez
This gene encodes a type I transmembrane glycoprotein that is an integral component of the multimeric gamma-secretase complex. The encoded protein cleaves integral membrane proteins, including Notch receptors and beta-amyloid precursor protein, and may be a stabilizing cofactor required for gamma-secretase complex assembly. The cleavage of beta-amyloid precursor protein yields amyloid beta peptide, the main component of the neuritic plaque and the hallmark lesion in the brains of patients with Alzheimer's disease; however, the nature of the encoded protein's role in Alzheimer's disease is not known for certain. Mutations in this gene are associated with familial acne inversa. A pseudogene of this gene is present on chromosome 21. Alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
Spécificité tissulaire
Detected in brain (at protein level) (PubMed:10993067). Widely expressed (PubMed:11396676).
Implication dans la maladie
Acne inversa, familial, 1: A chronic relapsing inflammatory disease of the hair follicles characterized by recurrent draining sinuses, painful skin abscesses, and disfiguring scars. Manifestations typically appear after puberty.
Similitudes de séquence
Belongs to the nicastrin family.
Modification post-traductionnelle
N-glycosylated.
Localisation cellulaire
Membrane. Cytoplasmic vesicle membrane. Melanosome.
Identified by mass spectrometry in melanosome fractions from stage I to stage IV.