Product Information
Molecular Weight74270Da
Protein NameAmiloride-sensitive sodium channel subunit gamma
Human Gene Id6340
Human Swiss Prot NoP51170
Mouse Gene Id20278
Mouse Swiss Prot NoQ9WU39
Rat Gene Id24768
Rat Swiss Prot NoP37091
SpecificityENaC γ Polyclonal Antibody detects endogenous levels of ENaC γ protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Concentration1 mg/ml
Storage Stability-20°C/1 year
Other NameSCNN1G; Amiloride-sensitive sodium channel subunit gamma; Epithelial Na(+) channel subunit gamma; ENaCG; Gamma-ENaC; Gamma-NaCH; Nonvoltage-gated sodium channel 1 subunit gamma; SCNEG
Observed Band(KD)80
Functiondisease:Defects in SCNN1G are a cause of Liddle syndrome [MIM:177200]. It is an autosomal dominant disorder characterized by pseudoaldosteronism and hypertension associated with hypokalemic alkalosis. The disease is caused by constitutive activation of the renal epithelial sodium channel.,function:Sodium permeable non-voltage-sensitive ion channel inhibited by the diuretic amiloride. Mediates the electrodiffusion of the luminal sodium (and water, which follows osmotically) through the apical membrane of epithelial cells. Controls the reabsorption of sodium in kidney, colon, lung and sweat glands. Also plays a role in taste perception.,PTM:Phosphorylated on serine and threonine residues.,PTM:Ubiquitinated; this targets individual subunits for endocytosis and proteasome-mediated degradation.,similarity:Belongs to the amiloride-sensitive sodium channel family.,subcellular location:Apical me
Subcellular LocationApical cell membrane ; Multi-pass membrane protein . Apical membrane of epithelial cells. .
ExpressionExpressed in kidney (at protein level).
Backgroundsodium channel epithelial 1 gamma subunit(SCNN1G) Homo sapiens Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the gamma subunit, and mutations in this gene have been associated with Liddle syndrome. [provided by RefSeq, Apr 2009],