Date published: 2026-6-6

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ZNF862 Antibody (A-6): sc-398768

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Datasheets
  • ZNF862 Antibody (A-6) is a mouse monoclonal IgM κ ZNF862 antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 1068-1096 near the C-terminus of ZNF862 of human origin
  • recommended for detection of ZNF862 of and human origin by WB, IP, IF and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for ZNF862 Antibody (A-6). This work is in progress.
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    ZNF862 Antibody (A-6) is a mouse monoclonal IgM antibody that detects ZNF862 of human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-ZNF862 antibody (A-6) is available as the non-conjugated form. ZNF862, also known as zinc finger protein 862, is a crucial nuclear protein composed of 1,169 amino acids that plays a significant role in transcriptional regulation. ZNF862 belongs to the Krüppel C2H2-type zinc-finger protein family, characterized by thirteen C2H2-type zinc fingers and a KRAB domain, which is believed to interact with KAP1, facilitating the recruitment of histone-modifying proteins that influence chromatin structure and gene expression. Proper functioning of ZNF862 is vital for maintaining normal cellular processes, as dysregulation can lead to various genetic disorders. ZNF862 is encoded on human chromosome 7, a region associated with several genetic conditions, including Osteogenesis imperfecta and Shwachman-Diamond syndrome. Notably, deletions in this chromosome have been linked to Williams-Beuren syndrome, which presents with cognitive challenges and distinctive physical features. ZNF862′s ability to modulate transcriptional activity underscores its importance in cellular homeostasis and highlights the potential implications of its dysfunction in disease states.

    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

    ZNF862 Antibody (A-6) References:

    1. Molecular cloning of six novel Krüppel-like zinc finger genes from hematopoietic cells and identification of a novel transregulatory domain KRNB.  |  Han, ZG., et al. 1999. J Biol Chem. 274: 35741-8. PMID: 10585455
    2. Long-term audiological feature in Pendred syndrome caused by PDS mutation.  |  Iwasaki, S., et al. 2001. Arch Otolaryngol Head Neck Surg. 127: 705-8. PMID: 11405873
    3. Williams-Beuren syndrome diagnosis using fluorescence in situ hybridization.  |  Osborne, LR., et al. 2006. Methods Mol Med. 126: 113-28. PMID: 16930009
    4. Lissencephaly 1 linking to multiple diseases: mental retardation, neurodegeneration, schizophrenia, male sterility, and more.  |  Reiner, O., et al. 2006. Neuromolecular Med. 8: 547-65. PMID: 17028375
    5. [Williams-Beuren syndrome].  |  Gilbert-Dussardier, B. 2006. Rev Prat. 56: 2102-6. PMID: 17416045
    6. Therapy-related leukemia and myelodysplasia: susceptibility and incidence.  |  Leone, G., et al. 2007. Haematologica. 92: 1389-98. PMID: 17768113
    7. Context-dependent DNA recognition code for C2H2 zinc-finger transcription factors.  |  Liu, J. and Stormo, GD. 2008. Bioinformatics. 24: 1850-7. PMID: 18586699
    8. Multiple genes encoding zinc finger domains are expressed in human T cells.  |  Thiesen, HJ. 1990. New Biol. 2: 363-74. PMID: 2288909
    9. Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.  |  Tsipouras, P., et al. 1983. J Clin Invest. 72: 1262-7. PMID: 6313757
    10. Zinc fingers: conserved properties that can distinguish between spurious and actual DNA-binding motifs.  |  Rosenfeld, R. and Margalit, H. 1993. J Biomol Struct Dyn. 11: 557-70. PMID: 8129873
    11. Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19.  |  Rousseau-Merck, MF., et al. 1993. Hum Genet. 92: 583-7. PMID: 8262519
    12. Molecular anatomy of chromosome 7q deletions in myeloid neoplasms: evidence for multiple critical loci.  |  Liang, H., et al. 1998. Proc Natl Acad Sci U S A. 95: 3781-5. PMID: 9520444

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    ZNF862 Antibody (A-6)

    sc-398768
    200 µg/ml
    $322.00

    ZNF862 (A-6) Neutralizing Peptide

    sc-398768 P
    100 µg/0.5 ml
    $69.00

    What application is the blocking peptide sc-398768 P appropriate for?

    Asked by: Trav11
    Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
    Answered by: Technical Support
    Date published: 2017-02-27
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    Rated 5 out of 5 by from Very good Western blot data of ZNF862 expressionVery good Western blot data of ZNF862 expression in A549 whole cell lysate. -SCBT QC
    Date published: 2013-04-28
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    ZNF862 Antibody (A-6) is rated 5.0 out of 5 by 1.
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