Date published: 2025-11-24

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GOLPH3 Antibody (905CT9.1.1): sc-517333

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Datasheets
  • GOLPH3 Antibody (905CT9.1.1) is a mouse monoclonal IgG1 GOLPH3 antibody provided at 100 µg/ml
  • raised against purified His-tagged GOLPH3 protein fragment of human origin
  • recommended for detection of GOLPH3 of human origin by WBIP
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for GOLPH3 Antibody (905CT9.1.1). This work is in progress.

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    GOLPH3 Antibody (905CT9.1.1) is a mouse monoclonal IgG1 antibody that detects GOLPH3 protein of human origin by western blotting (WB) and immunoprecipitation (IP). Anti-GOLPH3 antibody (905CT9.1.1) is available as a non-conjugated format. GOLPH3, also known as golgi phosphoprotein 3, GOPP1, GPP34, or MIDAS, is a 298 amino acid protein that plays a crucial role in regulating protein trafficking within the Golgi apparatus, a vital cellular organelle responsible for processing and packaging proteins. GOLPH3 localizes to both cytoplasm and Golgi stack membrane, suggesting an integral role in maintaining proper protein flow through the secretory pathway, essential for cellular function and communication. Dysregulation of GOLPH3 has been implicated in various diseases, including cancer, where altered protein transport and secretion may contribute to tumor growth and metastasis. GOLPH3 undergoes post-translational modifications, including phosphorylation, which influences activity and protein interactions. GOLPH3 gene resides on human chromosome 5, a chromosome associated with several genetic disorders, highlighting GOLPH3′s importance in normal physiology and disease states.

    For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

    Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

    LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

    GOLPH3 Antibody (905CT9.1.1) References:

    1. Proteomics characterization of abundant Golgi membrane proteins.  |  Bell, AW., et al. 2001. J Biol Chem. 276: 5152-65. PMID: 11042173
    2. MIDAS/GPP34, a nuclear gene product, regulates total mitochondrial mass in response to mitochondrial dysfunction.  |  Nakashima-Kamimura, N., et al. 2005. J Cell Sci. 118: 5357-67. PMID: 16263763
    3. The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.  |  Dixon, MJ., et al. 1991. Am J Hum Genet. 49: 17-22. PMID: 1676560
    4. Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair.  |  Cleaver, JE., et al. 2007. Neuroscience. 145: 1300-8. PMID: 17055654
    5. A new genomic mechanism leading to cri-du-chat syndrome.  |  South, ST., et al. 2006. Am J Med Genet A. 140: 2714-20. PMID: 17103439
    6. Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome.  |  Du, HY., et al. 2007. Aging Cell. 6: 689-97. PMID: 17875000
    7. Signal-mediated dynamic retention of glycosyltransferases in the Golgi.  |  Tu, L., et al. 2008. Science. 321: 404-7. PMID: 18635803
    8. A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization.  |  Saltman, DL., et al. 1993. Genomics. 16: 726-32. PMID: 8325647

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    GOLPH3 Antibody (905CT9.1.1)

    sc-517333
    100 µg/ml
    $316.00