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GOLPH3 Antibody Blocking Pepti

de(bs-13488P)-500ug
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  • ¥880
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  • bs-13488P
  • 2025年10月16日
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      500ug

    产品编号bs-13488P
    英文名称GOLPH3 Antibody Blocking Peptide
    中文名称高尔基体磷蛋白3封闭多肽
    英文别名Coat protein GPP34; FLJ90675; Golgi peripheral membrane protein 1, 34 kDa; Golgi phosphoprotein 3 (coat protein); Golgi phosphoprotein 3; GOLP3_HUMAN; Golph3; GPP34; MIDAS; Mitochondrial DNA absence factor.
    纯化方法HPLC
    研究领域

    Signal Transduction > Protein Trafficking > Golgi Proteins

    Signal Transduction > Protein Trafficking > Vesicle Transport > Coat Proteins

    Tags & Cell Markers > Subcellular Markers > Organelles > Golgi

    亚基Homodimer. Interacts with VPS35.
    亚细胞定位Cell membrane. Endosome. Cytoplasm. Golgi apparatus > Golgi stack membrane. Mitochondrion intermembrane space.
    组织特异性Detected in muscle fibers of patients with mitochondrial diseases; not detected in normal muscle fibers.
    翻译后修饰Phosphorylated.
    相似性Belongs to the GOLPH3/VPS74 family.
    功能Involved in modulation of mTOR signaling. Involved in the regulation of mitochondrial lipids, leading to increase of mitochondrial mass. Potential oncogene.
    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The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. GOLPH3L (golgi phosphoprotein 3-like), also known as GPP34R, is a 285 amino acid cytoplasmic protein that localizes to the Golgi apparatus. Belonging to the GOLPH3/VPS74 family, GOLPH3L may have a regulatory role in Golgi trafficking. GOLPH3L is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

     

     

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