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CYSTM1 Antibody (1-RE17): sc-134288

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  • CYSTM1 Antibody (1-RE17) is a mouse monoclonal IgG2a κ CYSTM1 antibody provided at 100 µg/ml
  • raised against recombinant CYSTM1 protein of human origin
  • recommended for detection of CYSTM1 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 CYSTM1 Antibody (1-RE17). This work is in progress.
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    CYSTM1 Antibody (1-RE17) is a mouse monoclonal IgG2a kappa light chain antibody that detects CYSTM1 protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), and enzyme-linked immunosorbent assay (ELISA). Anti-CYSTM1 antibody (1-RE17) is available as the non-conjugated format. CYSTM1 plays a crucial role in cellular processes, particularly in the regulation of immune responses and inflammation. CYSTM1 interacts with various signaling pathways, which are essential for maintaining cellular homeostasis and responding to stress. Understanding CYSTM1 function is important because dysregulation has been implicated in several diseases, including autoimmune disorders and cancer. CYSTM1′s ability to modulate immune cell activity highlights potential as a therapeutic target, making research vital for advancing knowledge of immune system functioning and developing new treatment strategies.

    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

    CYSTM1 Antibody (1-RE17) References:

    1. Duodenal adenomatosis in familial adenomatous polyposis coli. A review of the literature and results from the Heidelberg Polyposis Register.  |  Kadmon, M., et al. 2001. Int J Colorectal Dis. 16: 63-75. PMID: 11355321
    2. 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
    3. 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
    4. 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
    5. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.  |  Herry, A., et al. 2007. Eur J Haematol. 78: 457-67. PMID: 17391336
    6. Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).  |  Aretz, S., et al. 2007. Hum Mutat. 28: 985-92. PMID: 17486639
    7. Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome.  |  Du, HY., et al. 2007. Aging Cell. 6: 689-97. PMID: 17875000
    8. Molecular mechanisms of skin aging: state of the art.  |  Makrantonaki, E. and Zouboulis, CC. 2007. Ann N Y Acad Sci. 1119: 40-50. PMID: 18056953
    9. Analysis and validation of diagnostic biomarkers and immune cell infiltration characteristics in pediatric sepsis by integrating bioinformatics and machine learning.  |  Zhang, WY., et al. 2023. World J Pediatr. 19: 1094-1103. PMID: 37115484
    10. Six potential biomarkers in septic shock: a deep bioinformatics and prospective observational study.  |  Kong, C., et al. 2023. Front Immunol. 14: 1184700. PMID: 37359526
    11. Single-cell profiling reveals the intratumor heterogeneity and immunosuppressive microenvironment in cervical adenocarcinoma.  |  Peng, Y., et al. 2025. Elife. 13: PMID: 40066698
    12. 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

    CYSTM1 Antibody (1-RE17)

    sc-134288
    100 µg/ml
    $339.00

    For Western Blot, is it recommended to use denatured or non-denatured conditions with C5orf32 (1-RE17): sc-134288 antibody?

    Asked by: Cweed
    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_5, d_28, h_14CST
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    Rated 5 out of 5 by from Good for Western BlotAntibody detects human CYSTM1 in HT-29 and human CYSTM1 transfected cell lysate by Western blot. -SCBT QC
    Date published: 2023-09-14
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    CYSTM1 Antibody (1-RE17) is rated 4.0 out of 5 by 2.
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