KCNJ6 anticorps

N° du produit ABIN7882007

Cet anticorps anti-KCNJ6 Monoclonal Souris (Clone KCNJ6-7558) (ABIN7882007) détecte spécifiquement KCNJ6 dans IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour KCNJ6 anticorps (ABIN7882007)

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

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp KCNJ6 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Classe de qualité: Carrier-free

Clone: KCNJ6-7558

Détail du produit anti-KCNJ6 anticorps

Fonction: GIRK2 Antibody / G protein activated inward rectifier potassium channel 2 (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: A recombinant fragment of human KCNJ6 protein was used as the immunogen for the GIRK2 antibody.

Isotype: IgG2, kappa

Information d'application

Indications d'application: Optimal dilution of the GIRK2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: -20 °C

Stockage commentaire: Aliquot the GIRK2 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur KCNJ6

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

Autre désignation: GIRK2

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. [provided by RefSeq, Apr 2015]

UniProt: P48051