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FAHD2A Antibody (H-11): sc-515367

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Datasheets
  • FAHD2A Antibody (H-11) is a mouse monoclonal IgG3 κ FAHD2A antibody provided at 200 µg/ml
  • raised against amino acids 160-279 mapping within an internal region of FAHD2A of human origin
  • recommended for detection of FAHD2A of mouse, rat and human origin by WB, IP, IF and ELISA
  • m-IgG3 BP-HRP is the preferred secondary detection reagent for FAHD2A Antibody (H-11) for WB applications. This reagent is now offered in a bundle with FAHD2A Antibody (H-11) (see ordering information below).
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    FAHD2A Antibody (H-11) is a mouse monoclonal IgG3 kappa light chain antibody that detects FAHD2A protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-FAHD2A antibody (H-11) is available as the non-conjugated form. FAHD2A protein, also known as CGI-105, is a 314 amino acid protein that possesses hydrolase activity and belongs to the fumarylacetoacetate hydrolase family. FAHD2A plays a crucial role in various metabolic processes, particularly in the breakdown of certain amino acids, which is essential for maintaining cellular homeostasis and preventing toxic metabolite accumulation. FAHD2A activity depends on calcium and magnesium ions as cofactors, highlighting these minerals′ importance in enzymatic reactions. FAHD2A is encoded by a gene located on human chromosome 2, a region housing over 1,400 genes and associated with various genetic disorders. Chromosome 2 has been implicated in conditions such as Harlequin ichthyosis and Alström syndrome, underscoring the importance of understanding chromosome 2-encoded proteins in human health and disease.

    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

    FAHD2A Antibody (H-11) References:

    1. An ATP-binding cassette gene (ABCG5) from the ABCG (White) gene subfamily maps to human chromosome 2p21 in the region of the Sitosterolemia locus.  |  Shulenin, S., et al. 2001. Cytogenet Cell Genet. 92: 204-8. PMID: 11435688
    2. Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.  |  Hearn, T., et al. 2002. Nat Genet. 31: 79-83. PMID: 11941370
    3. X-ray structure of fumarylacetoacetate hydrolase family member Homo sapiens FLJ36880.  |  Manjasetty, BA., et al. 2004. Biol Chem. 385: 935-42. PMID: 15551868
    4. Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.  |  Kelsell, DP., et al. 2005. Am J Hum Genet. 76: 794-803. PMID: 15756637
    5. Differential expression of murine CGI-105 gene in 3T3-L1 cells by adrenocorticotropic hormones.  |  Choi, H., et al. 2005. Cell Biol Int. 29: 177-9. PMID: 15774318
    6. Punctuated duplication seeding events during the evolution of human chromosome 2p11.  |  Horvath, JE., et al. 2005. Genome Res. 15: 914-27. PMID: 15965031
    7. Rescue of lethal hepatic failure by hepatized lymph nodes in mice.  |  Hoppo, T., et al. 2011. Gastroenterology. 140: 656-666.e2. PMID: 21070777
    8. Identification of FAH domain-containing protein 1 (FAHD1) as oxaloacetate decarboxylase.  |  Pircher, H., et al. 2015. J Biol Chem. 290: 6755-62. PMID: 25575590
    9. Structural and functional comparison of fumarylacetoacetate domain containing protein 1 in human and mouse.  |  Weiss, AKH., et al. 2020. Biosci Rep. 40: PMID: 32068790
    10. Investigating the causal association between obesity and risk of hepatocellular carcinoma and underlying mechanisms.  |  Chen, Z., et al. 2024. Sci Rep. 14: 15717. PMID: 38977823
    11. An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13.  |  Baldini, A., et al. 1993. Hum Genet. 90: 577-83. PMID: 8444464
    12. Mapping a gene involved in regulating dietary cholesterol absorption. The sitosterolemia locus is found at chromosome 2p21.  |  Patel, SB., et al. 1998. J Clin Invest. 102: 1041-4. PMID: 9727073

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    FAHD2A Antibody (H-11)

    sc-515367
    200 µg/ml
    $322.00

    FAHD2A Antibody (H-11): m-IgG3 BP-HRP Bundle

    sc-550624
    200 µg Ab; 40 µg BP
    $361.00

    I need to use an antibody to detect the protein in samples of canine origin. Do you know if FAHD2A (H-11): sc-515367 mouse monoclonal antibody will work?

    Asked by: Trav11
    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 Specific for FAHD2A in Western BlotThis antibody detects over-expressed mouse FAHD2A in transfected lysate sc-126823 and endogenous FAHD2A in human cell line Jurkat. Shown with Cruz Marker molecular weight standards, sc-2035. -SCBT QC
    Date published: 2023-09-14
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    FAHD2A Antibody (H-11) is rated 5.0 out of 5 by 1.
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