KCNK9 anticorps

N° du produit ABIN7264657

Détail du produit anti-KCNK9 anticorps

Antigène: KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNK9 est non-conjugé

Application: Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: A synthetic peptide of human KCNK9 (NP_001269463.1).

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

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 KCNK9

Antigène: KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))

Autre désignation: KCNK9 (KCNK9 Produits)

Synonymes: anticorps Task3, anticorps K2p9.1, anticorps KT3.2, anticorps TASK-3, anticorps TASK3, anticorps KCNK9, anticorps LOC799704, anticorps Kcnk9, anticorps task3, anticorps k2p9.1, anticorps task-3, anticorps kt3.2, anticorps potassium channel, subfamily K, member 9, anticorps potassium two pore domain channel subfamily K member 9, anticorps potassium channel, two pore domain subfamily K, member 9, anticorps potassium channel, two pore domain subfamily K, member 9 L homeolog, anticorps Kcnk9, anticorps KCNK9, anticorps kcnk9, anticorps kcnk9.L

Sujet: This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH -dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome. Alternative splicing results in multiple transcript variants.

ID gène: 51305

UniProt: Q9NPC2