ELK Bio
KIR3.2 rabbit pAb - ES15302
KIR3.2 rabbit pAb - ES15302
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KIR3.2 rabbit pAb
Sizes: 50μL, 100μL
Catalogue Numbers: ES15302-50, ES15302-100
Citations, Manuals and MSDS Available upon request.
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],
Alternate Name: 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)
Source: Rabbit
Applications: IHC; IF; WB
Dilution: IHC-p 1:50-200, WB 1:500-2000
Reactivity: Human; Mouse; Rat
Immunogen: Synthesized peptide derived from human KIR3.2
Storage and Stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Observed Band (KD): 48kD
Human Gene ID: 3763
Human SWISS Prot NO: P48051
Subcellular Location: Membrane; Multi-pass membrane protein.
Research Use Only
