This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.

Codice: E-AB-68357_60μL | Marca: Elabscience | Confezionamento: 60μL

Specie: Human;Mouse;RatIsotipo: IgGConiugazione: Unconjugated
Dettagli prodotto
  • Codice: E-AB-68357_60μL
  • Marca: Elabscience
  • Specie target: Human;Mouse;Rat
  • Host: Rabbit
  • Concentrazione: 1 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
  • Diluizione: WB 1:1000-1:2000
  • Simbolo target: Occludin
  • Ig target: OCLN;BLCPMG;PPP1R115;PTORCH1;occludin;Occludin
  • Area di ricerca: Cancer;Signal Transduction