Date published: 2026-8-18

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NHN1 Antibody (F-2): sc-514364

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Datasheets
  • NHN1 Antibody (F-2) is a mouse monoclonal IgM κ NHN1 antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 341-358 within an internal region of NHN1 of human origin
  • recommended for detection of NHN1 of mouse, rat 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 NHN1 Antibody (F-2). This work is in progress.
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    NHN1 Antibody (F-2) is a mouse monoclonal IgM kappa antibody that detects NHN1 protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). NHN1 (F-2) antibody is available as the non-conjugated form. NHN1 protein, also known as ZC3H18 (zinc finger CCCH domain-containing protein 18), is a crucial nuclear protein composed of 953 amino acids, featuring one C3H1-type zinc finger and existing in two alternatively spliced isoforms. NHN1 plays a significant role in RNA metabolism and regulation, which is vital for maintaining cellular homeostasis and responding to stress. NHN1 gene is located on human chromosome 16q24.2, a region associated with various genetic disorders, including giant axonal neuropathy, Rubinstein-Taybi syndrome, and Crohn′s disease, due to mutations in neighboring genes. Chromosome 16 encompasses over 900 genes and approximately 90 million base pairs, representing nearly 3% of the human genome. NHN1′s intricate interactions with other proteins involved in RNA processing underscore its importance in cellular function and disease mechanisms, making anti-NHN1 antibody (F-2) an essential tool for researchers studying gene expression and regulation in various biological contexts.

    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

    NHN1 Antibody (F-2) References:

    1. The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.  |  Bomont, P., et al. 2000. Nat Genet. 26: 370-4. PMID: 11062483
    2. Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene.  |  Kuhlenbäumer, G., et al. 2002. Neurology. 58: 1273-6. PMID: 11971098
    3. Genetics of inflammatory bowel disease: progress and prospects.  |  Mathew, CG. and Lewis, CM. 2004. Hum Mol Genet. 13 Spec No 1: R161-8. PMID: 14764625
    4. Advances in the genetics of inflammatory bowel disease.  |  Cho, JH. 2004. Curr Gastroenterol Rep. 6: 467-73. PMID: 15527676
    5. The Rubinstein-Taybi syndrome: occurrence in two sets of identical twins.  |  Baraitser, M. and Preece, MA. 1983. Clin Genet. 23: 318-20. PMID: 6682729
    6. Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.  |  Breuning, MH., et al. 1993. Am J Hum Genet. 52: 249-54. PMID: 8430691
    7. An unusual form of chronic neutropenia in a father and daughter with hypogammaglobulinaemia.  |  Mentzer, WC., et al. 1977. Br J Haematol. 36: 313-22. PMID: 889707

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    NHN1 Antibody (F-2)

    sc-514364
    200 µg/ml
    $322.00

    NHN1 (F-2) Neutralizing Peptide

    sc-514364 P
    100 µg/0.5 ml
    $69.00