Kir2.2 anticorps (C-Term)

N° du produit ABIN1537286

Détail du produit anti-Kir2.2 anticorps

Antigène: Kir2.2 (KCNJ12) (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12))

Épitope: AA 405-433, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Kir2.2 est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This KCNJ12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 405-433 amino acids from the C-terminal region of human KCNJ12.

Clone: RB36707

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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,-20 °C

Stockage commentaire: KCNJ12 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur Kir2.2

Antigène: Kir2.2 (KCNJ12) (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12))

Autre désignation: KCNJ12 (KCNJ12 Produits)

Synonymes: anticorps IRK-2, anticorps IRK2, anticorps KCNJN1, anticorps Kir2.2, anticorps Kir2.2v, anticorps hIRK, anticorps hIRK1, anticorps hkir2.2x, anticorps kcnj12x, anticorps Kir2.1, anticorps IRK, anticorps KIR2.2, anticorps MB-IRK2, anticorps potassium voltage-gated channel subfamily J member 12, anticorps ATP-sensitive inward rectifier potassium channel 12, anticorps potassium inwardly-rectifying channel, subfamily J, member 12, anticorps KCNJ12, anticorps LOC746628, anticorps Kcnj12

Sujet: This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17.

Poids moléculaire: 49001

ID gène: 3768, 100131509, 100290070

NCBI Accession: NP_066292

UniProt: Q14500