KIR3.2 Polyclonal Antibody

Sizes: 50μL, 100μL

Catalogue Numbers: RA26661-50, RA26661-100

Citations, Manuals and MSDS Available upon request.

Background: potassium voltage-gated channel subfamily J member 6 (KCNJ6) Homo sapiens 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],

Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Storage Instructions: -20°C/1 year

Recommended dilutions: IHC-p 1:50-200, WB 1:500-2000

Alternative Names: G protein-activated inward rectifier potassium channel 2 (GIRK-2;BIR1;Inward rectifier K (+) channel Kir3.2;KATP-2;Potassium channel, inwardly rectifying subfamily J member 6)

Applications: IHC-p; IF (paraffin section) ; WB

Species Cross-Reactivity: Human; Mouse; Rat

GeneID (Human): 3763

Protein MW (KDa): 48

SWISS: P48051

Source: Rabbit

Research Use Only