KCNT1 anticorps (AA 1019-1068)

N° du produit ABIN1535188

L’anticorps anti-KCNT1 Polyclonal Lapin est utilisé pour la détection de KCNT1 dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB, IHC, ELISA et IF.

Aperçu rapide pour KCNT1 anticorps (AA 1019-1068) (ABIN1535188)

Antigène: KCNT1 (Potassium Channel, Subfamily T, Member 1 (KCNT1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNT1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Détail du produit anti-KCNT1 anticorps

Épitope: AA 1019-1068

Fonction: KCNT1 Antibody

Specificité: KCNT1 Polyclonal Antibody detects endogenous levels of KCNT1 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human KCNT1. AA range:1019-1068

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur KCNT1

Antigène: KCNT1 (Potassium Channel, Subfamily T, Member 1 (KCNT1))

Autre désignation: KCNT1

Sujet:

Synonyms: KCNT1, KIAA1422, Potassium channel subfamily T member 1, KCa4.1

Background: Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume.This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012],

Gene Name: KCNT1

Protein Name: Potassium channel subfamily T member 1

Poids moléculaire: 138 kDa

ID gène: 57582

OMIM: 608167

UniProt: Q5JUK3