KCNJ6 antibody

Catalog No. ABIN7882010

The Mouse Monoclonal anti-KCNJ6 antibody (Clone KCNJ6-7557) (ABIN7882010) specifically detects KCNJ6 in IHC (p). The antibody is reactive with Human samples.

Quick Overview for KCNJ6 antibody (ABIN7882010)

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

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This KCNJ6 antibody is un-conjugated

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: KCNJ6-7557

Product Details anti-KCNJ6 Antibody

Purpose: KCNJ6 Antibody / GIRK2

Purification: Protein A/G affinity

Immunogen: A recombinant fragment of human protein was used as the immunogen for the KCNJ6 antibody.

Isotype: IgG2, kappa

Application Details

Application Notes: Optimal dilution of the KCNJ6 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

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: Aliquot the KCNJ6 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Target Details for KCNJ6

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

Alternative Name: KCNJ6

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. [provided by RefSeq, Apr 2015]

UniProt: P48051