MFN2 Antibody Blocking Peptide(bs-23685P)-500ug

MFN2 Antibody Blocking Peptide

(bs-23685P)-500ug
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  • ¥880
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  • bs-23685P
  • 2025年10月16日
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      500ug

    产品编号bs-23685P
    英文名称MFN2 Antibody Blocking Peptide
    中文名称线粒体融合蛋白Mfn2封闭多肽
    英文别名 CMT2A; CMT2A2; MARF; CPRP 1; CPRP1; Fzo; HSG; hyperplasia suppressor gene; Hypertension related protein 1; MFN 2; Mfn2; MFN2_HUMAN; Mitochondrial assembly regulatory factor; Mitofusin-2; Mitofusin2; Transmembrane GTPase MFN2.
    纯化方法HPLC
    研究领域

    Cancer > Cell Death > Apoptosis > Metabolism

    Cancer > Cell Death > Apoptosis > Mitochondrial

    Cell Biology > Apoptosis > Mitochondrial

    Metabolism > Pathways and Processes > Metabolism processes > Apoptosis

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitophagy fission and fusion

    Neuroscience > Neurology process > Neurodegenerative disease

    Signal Transduction > Metabolism > Mitochondrial

    Tags & Cell Markers > Subcellular Markers > Organelles > Mitochondria

    亚基Forms homomultimers and heteromultimers with MFN1.
    亚细胞定位Mitochondrion outer membrane; Multi-pass membrane protein.
    组织特异性Ubiquitous; expressed at low level. Highly expressed in heart and kidney.
    相似性Belongs to the mitofusin family.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料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. [provided by RefSeq, Jul 2008].

     

     

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