KCNJ6 antibody (AA 1-80)

Catalog No. ABIN6142742

Product Details anti-KCNJ6 Antibody

Target: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Binding Specificity: AA 1-80

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNJ6 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: MAKLTESMTN VLEGDSMDQD VESPVAIHQP KLPKQARDDL PRHISRDRTK RKIQRYVRKD GKCNVHHGNV RETYRYLTDI

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-80 of human KCNJ6 (NP_002231.1).

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 KCNJ6

Target: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Alternative Name: KCNJ6 (KCNJ6 Products)

Synonyms: kcnj6 antibody, BIR1 antibody, GIRK-2 antibody, GIRK2 antibody, KATP-2 antibody, KATP2 antibody, KCNJ7 antibody, KIR3.2 antibody, hiGIRK2 antibody, Kir3.2 antibody, weaver antibody, wv antibody, potassium voltage-gated channel subfamily J member 6 antibody, potassium channel, inwardly rectifying subfamily J, member 5 antibody, potassium inwardly-rectifying channel, subfamily J, member 6 antibody, KCNJ6 antibody, kcnj5 antibody, Kcnj6 antibody

Background: This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.,KCNJ6,BIR1,GIRK-2,GIRK2,KATP-2,KATP2,KCNJ7,KIR3.2,KPLBS,hiGIRK2,Neuroscience,Cell Type Marker,Neuron marker,KCNJ6

Molecular Weight: 48 kDa

Gene ID: 3763

UniProt: P48051