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MFN2 Polyclonal Antibody

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

货号:E-AB-32025

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC-p

  • 详情
  • 文献(1)
  • Overview

    Synonyms CMT2A,CMT2A2,CPRP 1,CPRP1,EC 3.6.5.-,Fzo,HSG,hyperplasia suppressor gene,Hypertension related protein 1,KIAA0214,MARF,MFN 2,Mfn2,MFN2,Mitochondrial assembly regulatory factor,Mitofusin-2,Mitofusin2,Transmembrane GTPase MFN2,Mfn2抗体
    Swissprot O95140
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Synthesized peptide derived from the Internal region of human Mfn2.
    Application WB(Detection kit: E-IR-R304),IHC-p(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:100-1:300;
    Concentration 1mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Mitochondrion outer membrane. Colocalizes with BAX during apoptosis.
    Tissue specificity Ubiquitous; expressed at low level. Highly expressed in heart and kidney.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide, 0.5% BSA and 50% glycerol, pH7.4
    Background This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified.
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