KCNJ2 anticorps

N° du produit ABIN7245515

Détail du produit anti-KCNJ2 anticorps

Antigène: KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNJ2 est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of human KCNJ2

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.72 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 KCNJ2

Antigène: KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))

Autre désignation: KCNJ2 (KCNJ2 Produits)

Synonymes: anticorps KCNJ2, anticorps ATFB9, anticorps HHBIRK1, anticorps HHIRK1, anticorps IRK1, anticorps KIR2.1, anticorps LQT7, anticorps SQT3, anticorps Kir2.1, anticorps Kcnf1, anticorps IRK-1, anticorps potassium voltage-gated channel subfamily J member 2, anticorps potassium inwardly-rectifying channel, subfamily J, member 2, anticorps KCNJ2, anticorps Kcnj2

Sujet: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 48 kDa

UniProt: P63252