Date published: 2026-9-19

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GATSL3 Antibody (A-6): sc-377114

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Datasheets
  • GATSL3 Antibody (A-6) is a mouse monoclonal IgM κ GATSL3 antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 127-155 within an internal region of GATSL3 of human origin
  • recommended for detection of GATSL3 of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for GATSL3 Antibody (A-6). This work is in progress.
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    GATSL3 (A-6) is a mouse monoclonal IgM kappa antibody that detects GATSL3 protein of mouse, rat and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), immunohistochemistry with paraffin-embedded sections (IHCP) and enzyme-linked immunosorbent assay (ELISA). Anti-GATSL3 antibody (A-6) is available as the non-conjugated form. GATSL3 (GATS-like protein 3) is a 329 amino acid protein that belongs to the GATS family. The gene encoding GATSL3 maps to human chromosome 22, which contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

    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

    GATSL3 Antibody (A-6) References:

    1. Chromosome 22 workshop report.  |  Schwab, SG. and Wildenauer, DB. 1999. Am J Med Genet. 88: 276-8. PMID: 10374745
    2. Disease genes and chromosomes: disease maps of the human genome. Chromosome 22.  |  Gilbert, F. 1998. Genet Test. 2: 89-97. PMID: 10464604
    3. Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.  |  Tsilchorozidou, T., et al. 2004. J Med Genet. 41: 529-34. PMID: 15235024
    4. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.  |  Paylor, R., et al. 2006. Proc Natl Acad Sci U S A. 103: 7729-34. PMID: 16684884
    5. Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.  |  Arinami, T. 2006. J Hum Genet. 51: 1037-1045. PMID: 16969581
    6. Mutational spectrum of the NF2 gene: a meta-analysis of 12 years of research and diagnostic laboratory findings.  |  Ahronowitz, I., et al. 2007. Hum Mutat. 28: 1-12. PMID: 16983642
    7. BCR and its mutants, the reciprocal t(9;22)-associated ABL/BCR fusion proteins, differentially regulate the cytoskeleton and cell motility.  |  Zheng, X., et al. 2006. BMC Cancer. 6: 262. PMID: 17090304
    8. Deletion 22q11: spectrum of associated disorders.  |  Hay, BN. 2007. Semin Pediatr Neurol. 14: 136-9. PMID: 17980310

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    GATSL3 Antibody (A-6)

    sc-377114
    200 µg/ml
    $322.00

    GATSL3 Antibody (A-6): m-IgGκ BP-HRP Bundle

    sc-551782
    200 µg Ab; 40 µg BP
    $361.00

    GATSL3 (A-6) Neutralizing Peptide

    sc-377114 P
    100 µg/0.5 ml
    $69.00