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ACADM Antibody Blocking Peptid

e(bs-4047P)-500ug
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  • bs-4047P
  • 2025年10月16日
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      500ug

    产品编号bs-4047P
    英文名称ACADM Antibody Blocking Peptide
    中文名称酰基辅酶A脱氢酶中链封闭多肽
    英文别名mitochondrial antibody; ACAD 1; ACAD1; Acyl coenzyme A dehydrogenase; Acyl coenzyme A dehydrogenase C 4 to C 12 straight chain; MCAD; MCADH; Medium chain acyl CoA dehydrogenase; Medium chain fatty acyl CoA dehydrogenase; Medium chain specific acyl CoA dehydrogenase; Medium chain specific acyl CoA dehydrogenase mitochondrial; FLJ18227; FLJ93013; FLJ99884; ACADM_HUMAN.
    纯化方法HPLC
    研究领域

    Cancer > Cancer Metabolism > Metabolic signaling pathway > Metabolism of lipids and lipoproteins

    Cardiovascular > Lipids / Lipoproteins > Fatty Acids > Metabolism

    Metabolism > Pathways and Processes > Metabolic signaling pathways > Lipid and lipoprotein metabolism > Lipid metabolism

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers

    Metabolism > Pathways and Processes > Redox metabolism > Fatty acid oxidation

    Metabolism > Types of disease > Cancer

    Signal Transduction > Metabolism > Lipid metabolism

    Signal Transduction > Metabolism > Mitochondrial

    亚基Homotetramer. Interacts with the heterodimeric electron transfer flavoprotein ETF.
    亚细胞定位Mitochondrion matrix.
    相似性Belongs to the acyl-CoA dehydrogenase family.
    功能This enzyme is specific for acyl chain lengths of 4 to 16.
    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 the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

     

     

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