Anticorps epithelial Sodium Channel gamma

7 produits

epithelial Sodium Channel gamma est un gène codé par le symbole SCNN1G. D'autres noms incluent: Amiloride-sensitive sodium channel subunit gamma; Epithelial Na(+) channel subunit gamma; ENaCG; Gamma-NaCH; Nonvoltage-gated sodium channel 1 subunit gamma; SCNEG; SCNN1G. epithelial Sodium Channel gamma a une masse de 74.27kDa, une longueur d'acide aminé de 649, et est impliqué dans les maladies: Liddle syndrome 2; Bronchiectasis with or without elevated sweat chloride 3.

Nous proposons 7 des anticorps contre epithelial Sodium Channel gamma, élevé dans Lapin et Chèvre, qui sont appropriés pour le WB, IHC, ELISA et ICC/IF avec des échantillons dérivés de Humain, Souris, Rat, Hamster et Xenopus.

Informations sur les Gènes et les Protéines

Résumé UniProt
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. Plays an essential role in electrolyte and blood pressure homeostasis, but also in airway surface liquid homeostasis, which is important for proper clearance of mucus. Controls the reabsorption of sodium in kidney, colon, lung and sweat glands. Also plays a role in taste perception.
Résumé Entrez
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.
Spécificité tissulaire
Expressed in kidney (at protein level).
Implication dans la maladie
Liddle syndrome 2: A form of Liddle syndrome, an autosomal dominant disorder characterized by early onset of hypertension, hypokalemic alkalosis, and suppression of plasma renin activity and aldosterone secretion.

Bronchiectasis with or without elevated sweat chloride 3: A debilitating respiratory disease characterized by chronic, abnormal dilatation of the bronchi and other cystic fibrosis-like symptoms in the absence of known causes of bronchiectasis (cystic fibrosis, autoimmune diseases, ciliary dyskinesia, common variable immunodeficiency, foreign body obstruction). Clinical features include sub-normal lung function, sinopulmonary infections, chronic productive cough, excessive sputum production, and elevated sweat chloride in some cases.
Similitudes de séquence
Belongs to the amiloride-sensitive sodium channel (TC 1.A.6) family. SCNN1G subfamily.
Modification post-traductionnelle
Phosphorylated on serine and threonine residues. Aldosterone and insulin increase the basal level of phosphorylation.
Localisation cellulaire
Apical cell membrane.

Apical membrane of epithelial cells.
Western Blot - Anti-SCNN1G Antibody (A305215) - Antibodies.com
(3)
Western Blot - Anti-SCNN1G Antibody (A91086) - Antibodies.com
(3)
Western Blot - Anti-ENaC gamma Antibody (R12-2131) - Antibodies.com
(2)
Voir le roduitTaille d'Essai de 10µg
Western Blot - Anti-SCNN1G Antibody (A15078) - Antibodies.com
(2)
Immunohistochemistry - Anti-SCNN1G Antibody (A286000) - Antibodies.com
Anti-SCNN1G Antibody from Bioworld Technology (BS7921) - Antibodies.com
(2)
SCNN1G Antibody from Signalway Antibody (43516) - Antibodies.com

Affichage de 1-7 sur 7 produits

Filtres Menu Principal Nous Contacter 0Caisse
Haut