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KCNA1 Polyclonal Antibody

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

货号:E-AB-12529

宿主: Rabbit

反应性: H,M,R

应用: WB

  • 详情
  • Overview

    Synonyms AEMK,EA1,Episodic ataxia with myokymia,HBK1,HUK1,Kca1 1,Kcna1,KCNA1,Kcpvd,KV1.1,MBK1,mceph,MGC124402,MGC126782,MGC138385,MK1,MK1,mouse,homolog of KV1.1,Potassium channel protein 1,Potassium voltage gated channel shaker related subfamily member 1,Potassium voltage gated channel subfamily A member 1,Potassium voltage gated channel,shaker related subfamily,member 1 (episodic ataxia with myokymia),Potassium voltage-gated channel subfamily A member 1,RBK1,RCK1,Shak,Shaker related subfamily member 1,Voltage gated potassium channel subunit Kv1.1,Voltage-gated K(+) channel HuKI,Voltage-gated potassium channel HBK1,Voltage-gated potassium channel subunit Kv1.1,KCNA1抗体
    Swissprot Q09470
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Synthetic peptide of human KCNA1
    Application WB(Detection kit: E-IR-R304)
    Recommended dilution WB,,1:500-1:2000;
    Concentration 0.4 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Membrane.
    Tissue specificity Detected adjacent to nodes of Ranvier in juxtaparanodal zones in spinal cord nerve fibers, but also in paranodal regions in some myelinated spinal cord axons (at protein level) (PubMed:11086297). Detected in the islet of Langerhans (PubMed:21483673).
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background This gene encodes a voltage-gated delayed potassium channel that is phylogenetically related to the Drosophila Shaker channel. The encoded protein has six putative transmembrane segments (S1-S6), and the loop between S5 and S6 forms the pore and contains the conserved selectivity filter motif (GYGD). The functional channel is a homotetramer. The N-terminus of the channel is associated with beta subunits that can modify the inactivation properties of the channel as well as affect expression levels. The C-terminus of the channel is complexed to a PDZ domain protein that is responsible for channel targeting. Mutations in this gene have been associated with myokymia with periodic ataxia (AEMK).
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