KCNT1 anticorps

N° du produit ABIN7251640

Détail du produit anti-KCNT1 anticorps

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: Immunohistochemistry (IHC), ELISA

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of human KCNT1

Isotype: IgG

Information d'application

Indications d'application: IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.9 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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. Avoid freeze / thaw cycles.

Détails sur KCNT1

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

Autre désignation: KCNT1 (KCNT1 Produits)

Synonymes: anticorps EIEE14, anticorps ENFL5, anticorps KCa4.1, anticorps SLACK, anticorps bA100C15.2, anticorps Slack, anticorps rSlo2, anticorps C030030G16Rik, anticorps mKIAA1422, anticorps slo2, anticorps slack, anticorps Slo2.2, anticorps MGC146594, anticorps potassium sodium-activated channel subfamily T member 1, anticorps potassium channel subfamily T member 1, anticorps potassium channel, subfamily T, member 1, anticorps potassium channel, sodium activated subfamily T, member 1, anticorps KCNT1, anticorps LOC100436526, anticorps Kcnt1, anticorps kcnt1

Sujet: 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.

UniProt: Q5JUK3