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KIR2.1 Polyclonal Antibody, 100μg, (ATB-T2473)

$199.00
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Background: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]Product datasheet: Overview Product Description KIR2.1 Polyclonal Antibody, 100μg, (ATB-T2473) Image Species Reactivities Human,Rat Immunogen Synthesized peptide derived from the Internal region of human KIR2.1. Properties Form Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. Storage Instructions-20°C/1 year References: KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmia. Kalscheur MM, et al. Heart Rhythm, 2014 May. PMID 24561538 Free PMC Article Andersen-Tawil syndrome: clinical and molecular aspects. Nguyen HL, et al. Int J Cardiol, 2013 Dec 5. PMID 24383070 ESCRT regulates surface expression of the Kir2.1 potassium channel. Kolb AR, et al. Mol Biol Cell, 2014 Jan. PMID 24227888 Free PMC Article Novel mutation in the KCNJ2 gene is associated with a malignant arrhythmic phenotype of Andersen-Tawil syndrome. Fernlund E, et al. Ann Noninvasive Electrocardiol, 2013 Sep. PMID 24047492 Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation. Delannoy E, et al. Europace, 2013 Dec. PMID 23867365

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KIR2.1 Polyclonal Antibody, 100μg, (ATB-T2473)
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