Date published: 2026-5-8

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WBSCR11 Antibody (GTF5I102): sc-81425

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Datasheets
  • WBSCR11 Antibody (GTF5I102) is a mouse monoclonal IgG1 WBSCR11 antibody provided at 100 µg/ml
  • raised against a recombinant protein corresponding to an internal region of WBSCR11 of human origin
  • recommended for detection of WBSCR11 of human origin by WB, IP and IF
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for WBSCR11 Antibody (GTF5I102). This work is in progress.
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    WBSCR11 Antibody (GTF5I102) is a mouse monoclonal IgG1 antibody that detects WBSCR11 protein of human origin by western blotting (WB), immunoprecipitation (IP), and immunofluorescence (IF). Anti-WBSCR11 antibody (GTF5I102) is available as the non-conjugated format. The WBSCR11 gene, located within the critical deletion region associated with Williams-Beuren syndrome (WBS), encodes a transcription factor that plays a crucial role in regulating gene expression during development. WBSCR11 is essential for proper cellular function, interacting with various transcriptional machinery proteins to facilitate target gene transcription vital for normal growth and development. Loss of WBSCR11 due to hemizygous microdeletion on chromosome 7q11.23 contributes to developmental symptoms in WBS, including cognitive impairments and distinctive physical traits. WBSCR11 shows expression in all adult tissues and specific patterns during embryogenesis, highlighting developmental importance. WBSCR11′s carboxy terminus binds to retinoblastoma protein, suggesting involvement in cell cycle regulation crucial for maintaining normal cellular proliferation and differentiation.

    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

    WBSCR11 Antibody (GTF5I102) References:

    1. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.  |  Osborne, LR., et al. 1999. Genomics. 57: 279-84. PMID: 10198167
    2. Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.  |  Bellugi, U., et al. 1999. Trends Neurosci. 22: 197-207. PMID: 10322491
    3. Williams-Beuren syndrome: an update and review for the primary physician.  |  Lashkari, A., et al. 1999. Clin Pediatr (Phila). 38: 189-208. PMID: 10326175
    4. A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome.  |  Tassabehji, M., et al. 1999. Eur J Hum Genet. 7: 737-47. PMID: 10573005
    5. Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I.  |  Yan, X., et al. 2000. Biochem J. 345 Pt 3: 749-57. PMID: 10642537
    6. Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains.  |  Bayarsaihan, D. and Ruddle, FH. 2000. Proc Natl Acad Sci U S A. 97: 7342-7. PMID: 10861001
    7. Natural history of Williams syndrome: physical characteristics.  |  Morris, CA., et al. 1988. J Pediatr. 113: 318-26. PMID: 2456379

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    WBSCR11 Antibody (GTF5I102)

    sc-81425
    100 µg/ml
    $339.00

    What is the total volume provided of WBSCR11 (GTF5I102): sc-81425 monoclonal antibody?

    Asked by: Trav11
    Thank you for your question. WBSCR11 (GTF5I102): sc-81425 is provided as 100 µg in 1 ml total volume.
    Answered by: Technical Support
    Date published: 2017-03-06
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    Rated 5 out of 5 by from Good for Western BlotThis antibody detects a band at the expected molecular weight in human cell line HeLa. -SCBT QC
    Date published: 2023-09-14
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    WBSCR11 Antibody (GTF5I102) is rated 5.0 out of 5 by 2.
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