Date published: 2026-5-2

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PRPS1L1 Antibody (5E10): sc-517154

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  • PRPS1L1 Antibody (5E10) is a mouse monoclonal IgG3 κ PRPS1L1 antibody provided at 100 µg/ml
  • raised against amino acids 146-243 representing partial length PRPS1L1 of human origin
  • recommended for detection of PRPS1L1 of mouse, rat and human origin by WB, IP and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for PRPS1L1 Antibody (5E10). This work is in progress.
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    PRPS1L1 Antibody (5E10) is a mouse monoclonal IgG3 kappa light chain antibody that detects PRPS1L1 protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), and enzyme-linked immunosorbent assay (ELISA). Anti-PRPS1L1 antibody (5E10) is available as a non-conjugated format. PRPS1L1 protein, also known as phosphoribosyl pyrophosphate synthetase 3, is primarily localized in the testis, distinguishing PRPS1L1 from other PRPS isoforms that are ubiquitously expressed. This specific localization suggests a specialized role in testicular function and spermatogenesis, where PRPS1L1 is involved in the synthesis of phosphoribosyl pyrophosphate (PRPP), a key substrate for nucleotide biosynthesis. The production of PRPP is vital for the formation of nucleotides, which are essential for DNA and RNA synthesis, thereby influencing cellular proliferation and metabolism. Mutations in the gene encoding PRPS1L1 can lead to various disorders, including Charcot-Marie-Tooth disease X-linked recessive type 5, highlighting the importance of PRPS1L1 in maintaining normal cellular functions. With proven detection capabilities across multiple species and applications, PRPS1L1 (5E10) antibody serves as a valuable tool for researchers studying nucleotide metabolism and related pathologies.

    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

    PRPS1L1 Antibody (5E10) References:

    1. Accelerated transcription of PRPS1 in X-linked overactivity of normal human phosphoribosylpyrophosphate synthetase.  |  Ahmed, M., et al. 1999. J Biol Chem. 274: 7482-8. PMID: 10066814
    2. Phosphoribosylpyrophosphate synthetase overactivity as a cause of uric acid overproduction in a young woman.  |  García-Pavía, P., et al. 2003. Arthritis Rheum. 48: 2036-41. PMID: 12847698
    3. Promoter regions of the human X-linked housekeeping genes PRPS1 and PRPS2 encoding phosphoribosylpyrophosphate synthetase subunit I and II isoforms.  |  Ishizuka, T., et al. 1992. Biochim Biophys Acta. 1130: 139-48. PMID: 1314091
    4. Phosphoribosyl pyrophosphate formation in the rat adrenal gland in relation to adrenal growth in experimental diabetes.  |  Kunjara, S., et al. 1992. Diabetes. 41: 1429-35. PMID: 1383069
    5. Expression, purification, crystallization and preliminary X-ray diffraction analysis of human phosphoribosyl pyrophosphate synthetase 1 (PRS1).  |  Tang, W., et al. 2006. Acta Crystallogr Sect F Struct Biol Cryst Commun. 62: 432-4. PMID: 16682768
    6. Crystal structure of human phosphoribosylpyrophosphate synthetase 1 reveals a novel allosteric site.  |  Li, S., et al. 2007. Biochem J. 401: 39-47. PMID: 16939420
    7. Arts syndrome is caused by loss-of-function mutations in PRPS1.  |  de Brouwer, AP., et al. 2007. Am J Hum Genet. 81: 507-18. PMID: 17701896
    8. Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5).  |  Kim, HJ., et al. 2007. Am J Hum Genet. 81: 552-8. PMID: 17701900
    9. Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.  |  Ali, G., et al. 2011. Hum Hered. 71: 106-12. PMID: 21734401
    10. Proteomics analysis to reveal biological pathways and predictive proteins in the survival of high-grade serous ovarian cancer.  |  Xie, H., et al. 2017. Sci Rep. 7: 9896. PMID: 28852147
    11. Prps1l1, a testis-specific gene, is dispensable for mouse spermatogenesis.  |  Wang, Z., et al. 2018. Mol Reprod Dev. 85: 802-804. PMID: 30113107
    12. [PRPP synthetase superactivity].  |  Fujimori, S. 1996. Nihon Rinsho. 54: 3309-14. PMID: 8976111

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    PRPS1L1 Antibody (5E10)

    sc-517154
    100 µg/ml
    $322.00

    For Western Blot, is it recommended to use denatured or non-denatured conditions with PRPS1L1 (5E10): sc-517154 antibody?

    Asked by: Dr Ninau Qelp
    Thank you for your question. We recommend this antibody for use in denatured Western Blot conditions. It has not been validated for use in non-denatured conditions. Please contact our Technical Service Department for further details or inquiries.
    Answered by: Technical Support
    Date published: 2017-03-27
    • y_2026, m_4, d_29, h_11CST
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    Rated 5 out of 5 by from Good for Western BlotAntibody detects PRPS1L1 in Raw 264.7, PC-12, NIH/3T3, and Hela cell lysates by Western blot -SCBT QC
    Date published: 2023-09-14
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    PRPS1L1 Antibody (5E10) is rated 5.0 out of 5 by 1.
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