Kir2.2 antibody (AA 354-433)

Catalog No. ABIN7269472

Product Details anti-Kir2.2 Antibody

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

Binding Specificity: AA 354-433

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Kir2.2 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: KCNJ12 Rabbit pAb

Sequence: TPRCSAKDLV ENKFLLPSAN SFCYENELAF LSRDEEDEAD GDQDGRSRDG LSPQARHDFD RLQAGGGVLE QRPYRRESEI

Cross-Reactivity: Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Kir2.2

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

Alternative Name: KCNJ12 (KCNJ12 Products)

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

Background: 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

Molecular Weight: 49kDa

Gene ID: 3768

UniProt: Q14500