SCCD Antibody Blocking Peptide(bs-8848P)-500ug

SCCD Antibody Blocking Peptide

(bs-8848P)-500ug
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  • bs-8848P
  • 2025年10月16日
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      500ug

    产品编号bs-8848P
    英文名称SCCD Antibody Blocking Peptide
    中文名称抑癌蛋白UBIAD1封闭多肽
    英文别名UBIAD1; RP4-796F18.1; SCCD; TERE 1; tere1; Transitional epithelia response protein; Transitional epithelial response protein 1; UbiA prenyltransferase domain containing 1; UbiA prenyltransferase domain containing protein 1; UbiA prenyltransferase domain-containing protein 1; UBIA1_HUMAN; UBIAD 1; Ubiad1.
    纯化方法HPLC
    研究领域

    Epigenetics and Nuclear Signaling > Transcription > Cancer susceptibility > Tumor Suppressors

    Tags & Cell Markers > Cell Type Markers > Tumor Associated

    亚细胞定位Endoplasmic reticulum membrane. Cytoplasm. Nucleus. Mitochondrion.
    组织特异性Ubiquitously expressed.
    相似性Belongs to the ubiA prenyltransferase family.
    功能Prenyltransferase that mediates the formation of menaquinone-4 (MK-4) and coenzyme Q10. MK-4 is a vitamin K2 isoform present at high concentrations in the brain, kidney and pancreas, and is required for endothelial cell development. Mediates the conversion of phylloquinone (PK) into MK-4, probably by cleaving the side chain of phylloquinone (PK) to release 2-methyl-1,4-naphthoquinone (menadione; K3) and then prenylating it with geranylgeranyl pyrophosphate (GGPP) to form MK-4. Also plays a role in cardiovascular development independently of MK-4 biosynthesis, by acting as a coenzyme Q10 biosyntetic enzyme: coenzyme Q10, also named ubiquinone, plays a important antioxidant role in the cardiovascular system. Mediates biosynthesis of coenzyme Q10 in the Golgi membrane, leading to protect cardiovascular tissues from NOS3/eNOS-dependent oxidative stress.
    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 protein thought to be involved in cholesterol and phospholipid metabolism. Mutations in this gene are associated with Schnyder crystalline corneal dystrophy. [provided by RefSeq, Oct 2008]

     

     

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