Rabbit polyclonal primary
Kir5.1 Antibody (ER1901-24)
Synthetic peptide within rat kir5.1 aa 300-350.
Mouse kidney tissue lysate, human liver tissue, 293.
Store at +4C after thawing. Aliquot store at -20C. Avoid repeated freeze / thaw cycles.
1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Peptide affinity purified.
6430410F18Rik antibody; AI132396 antibody; BIR9 antibody; Inward rectifier K channel Kir5.1 antibody; Inward rectifier K(+) channel Kir5.1 antibody; Inward rectifier potassium channel 16 antibody; IRK16 antibody; IRKG antibody; KCNJ16 antibody; MGC33717 antibody; Potassium channel inwardly rectifying subfamily J member 16 antibody; Potassium inwardly rectifying channel subfamily J member 16 antibody; RP23-218O16.1 antibody
Belongs to the inward rectifier-type potassium channel (TC 1.A.2.1) family. KCNJ16 subfamily.
Widely expressed, with highest levels in adult and fetal kidney (at protein level). In the kidney, expressed in the proximal and distal convoluted tubules, but not in glomeruli nor collecting ducts.
Potassium inwardly-rectifying channel, subfamily J, member 16 (KCNJ16) is a human gene encoding the Kir5.1 protein. Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. Kir5.1 is an integral membrane protein and inward-rectifier type potassium channel. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. KCNJ16 may be involved in the regulation of fluid and pH balance. In the kidney, together with KCNJ10, mediates basolateral K+ recycling in distal tubules; this process is critical for Na+ reabsorption at the tubules.