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: AN300884L_100μL | Marca: Elabscience | Confezionamento: 100μL

Specie: Human;Mouse;RatIsotipo: IgG,κClone: 5C7Coniugazione: Unconjugated
Dettagli prodotto
  • Codice: AN300884L_100μL
  • Marca: Elabscience
  • Specie target: Human;Mouse;Rat
  • Host: Rabbit
  • Concentrazione: 0.2 mg/mL
  • Link: Apri link
  • Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
  • Isotipo: IgG,κ
  • Clonalità: Monoclonal;Recombinant
  • Clone: 5C7
  • Coniugazione: Unconjugated
  • Applicazione: WB
  • Diluizione: WB 1:2000-1:10000
  • Simbolo target: OCLN
  • Ig target: PPP1R;PTORCH;OCLN;BLCPMG;PPP1R115;PTORCH1;occludin
  • Area di ricerca: Signal Transduction