This nuclear gene encodes a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. Since the gene for this enzyme maps close to that for Duchenne muscular dystrophy, it may play a role in that disease also.

Codice: E-AB-15274_200μL | Marca: Elabscience | Confezionamento: 200μL

Specie: Human;Mouse;RatIsotipo: IgGConiugazione: Unconjugated
Dettagli prodotto
  • Codice: E-AB-15274_200μL
  • Marca: Elabscience
  • Specie target: Human;Mouse;Rat
  • Host: Rabbit
  • Concentrazione: 0.3 mg/mL
  • Link: Apri link
  • Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
  • Isotipo: IgG
  • Clonalità: Polyclonal
  • Coniugazione: Unconjugated
  • Applicazione: WB;IHC
  • Diluizione: WB 1:500-1:2000;IHC 1:50-1:200
  • Simbolo target: OTC
  • Ig target: EC 2.1.3.3;MGC129967;MGC129968;MGC138856;OCTD;Ornithine carbamoyltransferase mitochondrial;Ornithine carbamoyltransferase;mitochondrial;Ornithine transcarbamylase;Otc;OTC;OTCase
  • Area di ricerca: Cancer;Metabolism;Signal Transduction;Tags and Cell Markers