Anti-KCNJ6 (Kir3.2 or GIRK2) antibody is validated on mouse tissue and recommended for immunofluorescence labeling, IHC, or western blot of materials from rodent and human tissues.
Potassium inwardly rectifying channel subfamily J member 6 (KCNJ6), also known as G-protein-gated inwardly-rectifying potassium channel member 2 (GIRK2) or Kir3.2, is an inward-rectifier type potassium channel that is encoded by the KCNJ6 gene in human. Mutations in the KCNJ6 gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.
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