KCNJ2 anticorps (AA 41-64) (Atto 390)

N° du produit ABIN2483529

Cet anticorps Souris Monoclonal détecte spécifiquement KCNJ2 dans WB, IHC, ICC, IF et AA. Il présente une réactivité avec des échantillons de Souris.

Aperçu rapide pour KCNJ2 anticorps (AA 41-64) (Atto 390) (ABIN2483529)

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

Reactivité: Souris

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp KCNJ2 est conjugé à/à la Atto 390

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), Immunofluorescence (IF), Antibody Array (AA)

Clone: S112

Détail du produit anti-KCNJ2 anticorps (Atto 390)

Épitope: AA 41-64

Specificité: Detects ~45 kDa. No cross-reactivity against Kir2.2 or Kir2.3.

Réactivité croisée: Humain, Singe, Souris, Rat

Purification: Protein G Purified

Immunogène: Fusion protein amino acids 41-64 and 189-428 of mouse Kir2.1

Isotype: IgG1

Information d'application

Indications d'application:

• WB (1:1000)
• IHC (1:1000)
• ICC/IF (1:100)
• optimal dilutions for assays should be determined by the user.

Commentaires:

1 μg/ml of ABIN2483529 was sufficient for detection of Kir2.1 in 10 μg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS pH 7.4, 50 % glycerol, 0.09 % sodium azide, Storage buffer may change when conjugated

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: 4 °C

Stockage commentaire: Conjugated antibodies should be stored at 4°C

Détails sur KCNJ2

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

Autre désignation: Kir2.1

Sujet: The Kir2.1 inward-rectifier potassium ion channel is encoded by the KCNJ2 gene. A defect in this gene is associated with Andersen-Tawil syndrome (1).

ID gène: 16518

NCBI Accession: NP_032451

UniProt: P35561