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SCO2 Antibody Blocking Peptide

(bs-17295P)-500ug
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  • bs-17295P
  • 2025年10月16日
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      500ug

    产品编号bs-17295P
    英文名称SCO2 Antibody Blocking Peptide
    中文名称细胞色素氧化酶缺失蛋白2封闭多肽
    英文别名Cytochrome oxidase deficient homolog 2; MGC125823; MGC125825; OTTHUMP00000196774; OTTHUMP00000196775; Protein SCO2 homolog, mitochondrial; SCO (cytochrome oxidase deficient, yeast) homolog 2; SCO 1L; SCO 2; SCO cytochrome oxidase deficient homolog 2 (yeast); SCO cytochrome oxidase deficient homolog 2; SCO1L; SCO2; SCO2_HUMAN; Synthesis of cytochrome c oxidase 2.
    纯化方法HPLC
    研究领域

    Metabolism > Pathways and Processes > Cofactors, Vitamins / minerals > Vitamins / minerals

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Oxidative phosphorylation > Complex IV

    Metabolism > Types of disease > Cancer

    Signal Transduction > Metabolism > Mitochondrial

    Signal Transduction > Metabolism > Vitamins / Minerals

    Tags & Cell Markers > Subcellular Markers > Organelles > Mitochondria

    亚细胞定位Mitochondrion.
    组织特异性Ubiquitous.
    相似性Belongs to the SCO1/2 family.
    Contains 1 thioredoxin domain.
    功能Acts as a copper chaperone, transporting copper to the Cu(A) site on the cytochrome c oxidase subunit II (COX2).
    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Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors; this gene encodes one of the COX asembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy. [provided by RefSeq, Dec 2009]

     

     

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