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WB analysis of human brain (substantia nigra) lysate using GTX88962 GIRK2 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain (substantia nigra) lysate using GTX88962 GIRK2 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain (substantia nigra) lysate using GTX88962 GIRK2 antibody, C-term. Dilution : 0.5microg/ml Loading : 35microg protein in RIPA buffer

GIRK2 antibody, C-term

GTX88962
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetKCNJ6
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Overview

  • Supplier
    GeneTex
  • Product Name
    GIRK2 antibody, C-term
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 2-6microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3763
  • Target name
    KCNJ6
  • Target description
    potassium inwardly rectifying channel subfamily J member 6
  • Target synonyms
    BIR1; G protein-activated inward rectifier potassium channel 2; GIRK2; GIRK-2; hiGIRK2; inward rectifier K(+) channel Kir3.2; inward rectifier potassium channel KIR3.2; KATP2; KATP-2; KCNJ7; KIR3.2; KPLBS; potassium channel, inwardly rectifying subfamily J, member 6; potassium voltage-gated channel subfamily J member 6
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP48051
  • Protein Name
    G protein-activated inward rectifier potassium channel 2
  • Scientific Description
    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]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203