Kir2.2 anticorps (AA 354-433)

N° du produit ABIN7269472

Détail du produit anti-Kir2.2 anticorps

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

Épitope: AA 354-433

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Kir2.2 est non-conjugé

Application: Western Blotting (WB)

Fonction: KCNJ12 Rabbit pAb

Séquence: TPRCSAKDLV ENKFLLPSAN SFCYENELAF LSRDEEDEAD GDQDGRSRDG LSPQARHDFD RLQAGGGVLE QRPYRRESEI

Réactivité croisée: Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 354-433 of human KCNJ12 (NP_066292.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

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 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.,KCNJ12,IRK-2,IRK2,KCNJN1,Kir2.2,Kir2.2v,hIRK,hIRK1,hkir2.2x,kcnj12x,KCNJ12

Poids moléculaire: 49kDa

ID gène: 3768

UniProt: Q14500