HCCS Antibody Blocking Peptide(bs-15424P)-500ug

HCCS Antibody Blocking Peptide

(bs-15424P)-500ug
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  • ¥880
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  • bs-15424P
  • 2025年10月16日
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      500ug

    产品编号bs-15424P
    英文名称HCCS Antibody Blocking Peptide
    中文名称全细胞色素C合成酶封闭多肽
    英文别名CCHL; DKFZp779I1858; EC 4.4.1.17; Holocytochrome c synthase (cytochrome c heme lyase); Holocytochrome c type synthase; MCOPS7; RGD1563855; RP23-37L2.1; CCHL_HUMAN.
    纯化方法HPLC
    研究领域

    Cardiovascular > Lipids / Lipoproteins > Lipid Metabolism > Cytochromes

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

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Cytochromes

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers

    Signal Transduction > Metabolism > Mitochondrial

    亚细胞定位Mitochondrion inner membrane (Potential).
    相似性Belongs to the cytochrome c-type heme lyase family.
    Contains 2 HRM (heme regulatory motif) repeats.
    功能Links covalently the heme group to the apoprotein of cytochrome c (By similarity).
    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HCCS is a 79 amino acid protein that may act as a tumor suppressor, promoting the apoptosis of cancer cells. Expressed in leukocytes, lung, spleen, liver, heart, kidney, muscle and uterine cervix, HCCS-1 is down-regulated in cervical cancers. The gene encoding HCCS-1 maps to human chromosome 15q25.1. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

     

     

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