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KCNJ2 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-18197

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC

  • 详情
  • Overview

    Synonyms Cardiac inward rectifier potassium channel,HHBIRK 1,HHBIRK1,HHIRK 1,HHIRK1,HIRK 1,hIRK1,Inward rectifier K,Inward rectifier K(+) channel Kir2.1,Inward rectifier potassium channel 2,inwardly rectifying subfamily J member 2,IRK 1,IRK-1,IRK1,IRK2,KCNJ2,KIR2.1,LQT 7,LQT7,Potassium channel,Potassium channel inwardly rectifying subfamily J member 2,Potassium inwardly rectifying channel J2,Potassium inwardly rectifying channel subfamily J member 2,SQT 3,SQT3,KCNJ2抗体
    Swissprot P63252
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Synthetic peptide of human KCNJ2
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:30-1:150;
    Concentration 0.72mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Membrane.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    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.
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