KCNJ6 anticorps

N° du produit ABIN7264952

Détail du produit anti-KCNJ6 anticorps

Antigène: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNJ6 est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human KCNJ6 (NP_002231.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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 KCNJ6

Antigène: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Autre désignation: KCNJ6 (KCNJ6 Produits)

Synonymes: anticorps kcnj6, anticorps BIR1, anticorps GIRK-2, anticorps GIRK2, anticorps KATP-2, anticorps KATP2, anticorps KCNJ7, anticorps KIR3.2, anticorps hiGIRK2, anticorps Kir3.2, anticorps weaver, anticorps wv, anticorps potassium voltage-gated channel subfamily J member 6, anticorps potassium channel, inwardly rectifying subfamily J, member 5, anticorps potassium inwardly-rectifying channel, subfamily J, member 6, anticorps KCNJ6, anticorps kcnj5, anticorps Kcnj6

Sujet: This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.

Poids moléculaire:

Observed_MW: 48 kDa

Calculated_MW: 48 kDa

ID gène: 3763

UniProt: P48051