Date published: 2025-10-16

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AMDHD1 Antibody (F-3): sc-515501

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Datasheets
  • AMDHD1 Antibody (F-3) is a mouse monoclonal IgM κ AMDHD1 antibody provided at 200 µg/ml
  • raised against amino acids 133-359 mapping within an internal region of AMDHD1 of human origin
  • recommended for detection of AMDHD1 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 AMDHD1 Antibody (F-3). This work is in progress.

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    AMDHD1 Antibody (F-3) is a mouse monoclonal IgM antibody that detects AMDHD1 of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-AMDHD1 antibody (F-3) is available as the non-conjugated monoclonal isotype antibody. AMDHD1, also known as probable imidazolonepropionase, consists of 426 amino acids and belongs to the hutI family, playing a crucial role in hydrolase activity that acts on carbon-nitrogen bonds, excluding peptide bonds, particularly in cyclic amides. AMDHD1 is essential for imidazolonepropionase activity and is involved in metal ion binding, specifically binding one iron or zinc ion per subunit, which is vital for enzymatic function. AMDHD1 is located on human chromosome 12, a region associated with various skeletal deformities and developmental disorders, including Noonan syndrome, which is characterized by heart and facial developmental defects. AMDHD1′s significance extends beyond enzymatic activity, as AMDHD1 is implicated in critical biological processes that can influence cellular function and development, making AMDHD1 a valuable target for research in both basic and clinical settings.

    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

    AMDHD1 Antibody (F-3) References:

    1. The genomic context of natural killer receptor extended gene families.  |  Trowsdale, J., et al. 2001. Immunol Rev. 181: 20-38. PMID: 11513141
    2. The phenotypic spectrum of COL2A1 mutations.  |  Nishimura, G., et al. 2005. Hum Mutat. 26: 36-43. PMID: 15895462
    3. Comparative genomics of natural killer cell receptor gene clusters.  |  Kelley, J., et al. 2005. PLoS Genet. 1: 129-39. PMID: 16132082
    4. Noonan syndrome.  |  van der Burgt, I. 2007. Orphanet J Rare Dis. 2: 4. PMID: 17222357
    5. [Mutation analysis of PTPN11 gene in Noonan syndrome].  |  Yang, T., et al. 2010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 27: 554-8. PMID: 20931536
    6. Low basal transcripts of the COL2A1 collagen gene from lymphoblasts show alternative splicing of exon 12 in the Kniest form of spondyloepiphyseal dysplasia.  |  Yang, W. and Cole, WG. 1998. Hum Mutat. Suppl 1: S1-2. PMID: 9452022

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    AMDHD1 Antibody (F-3)

    sc-515501
    200 µg/ml
    $316.00

    I need to use an antibody to detect the protein in samples of canine origin. Do you know if AMDHD1 (F-3): sc-515501 mouse monoclonal antibody will work?

    Asked by: cjMara
    Thank you for your inquiry. Please contact our Technical Service Department and we would be happy to perform sequence analysis and review our data to answer any questions you may have about additional species reactivity. We are available by phone, e-mail or chat.
    Answered by: Technical Support
    Date published: 2017-02-28
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    Rated 5 out of 5 by from Good for detecting AMDHD1 by Western BlotAntibody works well in human cell lines HepG2 and A549. -SCBT QC
    Date published: 2023-09-14
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    AMDHD1 Antibody (F-3) is rated 5.0 out of 5 by 1.
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