Date published: 2025-11-25

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TBCEL Antibody (AT1B10): sc-517427

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Datasheets
  • TBCEL Antibody (AT1B10) is a mouse monoclonal IgG2b κ TBCEL antibody provided at 100 µg/ml
  • raised against a recombinant protein corresponding to amino acids 1-424 of TBCEL of human origin
  • recommended for detection of TBCEL of human origin by WB, IF, FCM and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for TBCEL Antibody (AT1B10). This work is in progress.

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    TBCEL Antibody (AT1B10) is a mouse monoclonal IgG2b kappa light chain antibody that detects TBCEL protein of human origin by western blotting (WB), immunofluorescence (IF), flow cytometry (FCM), and enzyme-linked immunosorbent assay (ELISA). Anti-TBCEL antibody (AT1B10) is available as the non-conjugated format. TBCEL, or tubulin-folding cofactor E-like protein, is a crucial 424 amino acid cytoplasmic protein that plays a significant role in regulating tubulin stability, which is essential for maintaining the integrity of the cytoskeleton and facilitating cellular processes such as division and intracellular transport. TBCEL is predominantly expressed in the testis but is also found in various other tissues at lower levels, indicating potential involvement in diverse biological functions. Structurally, TBCEL features seven leucine-rich repeats, one LRRCT domain, and one ubiquitin-like domain, which are important for interactions and regulatory functions. The gene encoding TBCEL spans 66,704 bases and is located on human chromosome 11q23.3, a region associated with several genetic disorders, including Jervell and Lange-Nielsen syndrome and Jacobsen syndrome, highlighting TBCEL′s importance in human health and disease.

    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

    TBCEL Antibody (AT1B10) References:

    1. Hereditary angioedema. Long-term follow-up of 88 patients. Experience of the Argentine Allergy and Immunology Institute.  |  Fabiani, JE., et al. 2000. Allergol Immunopathol (Madr). 28: 267-71. PMID: 11270087
    2. Smith-Lemli-Opitz syndrome and the DHCR7 gene.  |  Jira, PE., et al. 2003. Ann Hum Genet. 67: 269-80. PMID: 12914579
    3. Identification of a novel tubulin-destabilizing protein related to the chaperone cofactor E.  |  Bartolini, F., et al. 2005. J Cell Sci. 118: 1197-207. PMID: 15728251
    4. The pathogenesis and treatment of acid sphingomyelinase-deficient Niemann-Pick disease.  |  Schuchman, EH. 2007. J Inherit Metab Dis. 30: 654-63. PMID: 17632693
    5. Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance.  |  Siem, G., et al. 2008. Ear Hear. 29: 261-9. PMID: 18595190
    6. Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).  |  Coldren, CD., et al. 2009. Neurogenetics. 10: 89-95. PMID: 18855024
    7. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.  |  Bhuiyan, ZA., et al. 2008. Prog Biophys Mol Biol. 98: 319-27. PMID: 19027783

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    TBCEL Antibody (AT1B10)

    sc-517427
    100 µg/ml
    $316.00