Alkaline Phosphatase è un gene codificato dal simbolo ALPL. Altri nomi includono: Alkaline phosphatase, tissue-nonspecific isozyme; AP-TNAP liver/bone/kidney isozyme; ALPL. Alkaline Phosphatase ha una massa di 57.31kDa, una lunghezza di amminoacidi di 524, ed è implicato nella malattia: Hypophosphatasia; Hypophosphatasia childhood type; Hypophosphatasia infantile type.
Offriamo 37 anticorpi contro Alkaline Phosphatase, allevati nel Coniglio, Topo, Capra e Sheep, che sono adatti per WB, IHC, ELISA, ICC/IF, Citometria a Flusso, IP e Dot con campioni derivati da Umano, Maiale, Scimmia, Pecora, Cane, E. coli e Goat.
Informazioni su geni e proteine
Riepilogo UniProt
This isozyme plays a key role in skeletal mineralization by regulating levels of diphosphate (PPi).
Sommario di Entrez
There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The intestinal alkaline phosphatase gene encodes a digestive brush-border enzyme. This enzyme is a component of the gut mucosal defense system and is thought to function in the detoxification of lipopolysaccharide, and in the prevention of bacterial translocation in the gut.
Coinvolgimento nella malattia
Hypophosphatasia: A metabolic bone disease characterized by defective skeletal mineralization and biochemically by deficient activity of the tissue non-specific isoenzyme of alkaline phosphatase. Four forms are distinguished, depending on the age of onset: perinatal, infantile, childhood and adult type. The perinatal form is the most severe and is almost always fatal. The adult form is mild and characterized by recurrent fractures, osteomalacia, rickets, and loss of teeth. Some cases are asymptomatic, while some patients manifest dental features without skeletal manifestations (odontohypophosphatasia).
Hypophosphatasia childhood type: A bone disease characterized by defective skeletal mineralization and biochemically by deficient activity of the tissue non-specific isoenzyme of alkaline phosphatase.
Hypophosphatasia infantile type: A severe bone disease characterized by defective skeletal mineralization and biochemically by deficient activity of the tissue non-specific isoenzyme of alkaline phosphatase. Three more or less distinct types of infantile hypophosphatasia can be identified: (1) type 1 with onset in utero or in early postnatal life, craniostenosis, severe skeletal abnormalities, hypercalcemia, and death in the first year or so of life; (2) type 2 with later, more gradual development of symptoms, moderately severe 'rachitic' skeletal changes and premature loss of teeth; (3) type 3 with no symptoms, the condition being determined on routine studies.
Somiglianze di sequenza
Belongs to the alkaline phosphatase family.
Modifica post-translazionale
N-glycosylated.
Posizione cellulare
Cell membrane.
