Date published: 2025-11-23

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STK32A Antibody (5H10): sc-135571

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Datasheets
  • STK32A Antibody (5H10) is a mouse monoclonal IgG1 κ STK32A antibody provided at 100 µg/ml
  • raised against recombinant STK32A protein of human origin
  • recommended for detection of STK32A of human origin by WB, IP and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for STK32A Antibody (5H10). This work is in progress.

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    STK32A Antibody (5H10) is a mouse monoclonal IgG1 kappa light chain antibody that detects STK32A protein of human origin by western blotting (WB), immunoprecipitation (IP), and enzyme-linked immunosorbent assay (ELISA). Anti-STK32A antibody (5H10) is available as a non-conjugated format. STK32A protein, also known as serine/threonine kinase 32A or YANK1, plays a crucial role in cellular signaling pathways by regulating various cellular processes through phosphorylation. This post-translational modification is vital for the activation and deactivation of proteins, influencing key functions such as cell division, differentiation, DNA repair, and transcription. STK32A protein consists of 396 amino acids and is part of the serine/threonine protein kinase superfamily, existing in three isoforms. The gene encoding STK32A is located on human chromosome 5, which is linked to several genetic disorders, including Cockayne syndrome and familial adenomatous polyposis, due to proximity to the ERCC8 and APC tumor suppressor genes, respectively. Additionally, abnormalities in chromosome 5, such as deletions, are associated with various syndromes and malignancies, highlighting STK32A′s importance in maintaining cellular integrity and function.

    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

    STK32A Antibody (5H10) References:

    1. Recent advances in myelodysplastic syndromes.  |  Shadduck, RK., et al. 2007. Exp Hematol. 35: 137-43. PMID: 17379099
    2. Translocations and mutations involving the nucleophosmin (NPM1) gene in lymphomas and leukemias.  |  Falini, B., et al. 2007. Haematologica. 92: 519-32. PMID: 17488663
    3. Fetal trisomy 5 mosaicism: case report and literature review.  |  Villa, N., et al. 2007. Am J Med Genet A. 143A: 2343-6. PMID: 17702005
    4. Chromosome 5q subtelomeric deletion syndrome.  |  Rauch, A. and Dörr, HG. 2007. Am J Med Genet C Semin Med Genet. 145C: 372-6. PMID: 17910075
    5. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.  |  Azman, BZ., et al. 2008. Singapore Med J. 49: e98-e100. PMID: 18418516
    6. Speech and language development in cri du chat syndrome: a critical review.  |  Kristoffersen, KE. 2008. Clin Linguist Phon. 22: 443-57. PMID: 18484284
    7. Mapping of 5q35 chromosomal rearrangements within a genomically unstable region.  |  Buysse, K., et al. 2008. J Med Genet. 45: 672-8. PMID: 18628311
    8. Revealing the pathogenesis of the 5q- syndrome.  |  Valent, P. 2008. Eur J Clin Invest. 38: 539-40. PMID: 18717823

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    STK32A Antibody (5H10)

    sc-135571
    100 µg/ml
    $333.00