Date published: 2025-11-21

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KIAA1191 Antibody (G-4): sc-398723

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Datasheets
  • KIAA1191 Antibody (G-4) is a mouse monoclonal IgM κ KIAA1191 antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 209-246 within an internal region of KIAA1191 of human origin
  • recommended for detection of KIAA1191 of human origin, 4833439L19Rik of mouse origin and the corresponding rat homolog by WB, IP, IF and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for KIAA1191 Antibody (G-4). This work is in progress.

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    KIAA1191 Antibody (G-4) is a mouse monoclonal IgM antibody that detects KIAA1191 in human, mouse, and rat samples through applications such as western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-KIAA1191 antibody (G-4) is available as a non-conjugated format. KIAA1191 is a 305 amino acid protein that belongs to the UPF0498 family and exists in three alternatively spliced isoforms, which may have distinct functions and regulatory mechanisms. The gene encoding KIAA1191 spans approximately 15,908 bases and is located on human chromosome 5q35.2, a region comprising nearly 6% of the human genome and associated with various genetic disorders. KIAA1191 plays a crucial role in cellular processes, including RNA metabolism and gene expression regulation, which are vital for maintaining cellular homeostasis and responding to environmental changes. Understanding KIAA1191 function is important, as dysregulation may contribute to the development of diseases, including certain cancers and genetic syndromes. KIAA1191′s interactions with other cellular proteins further underscore significance in complex biological pathways, making KIAA1191 (G-4) monoclonal antibody an essential tool for researchers investigating these critical processes.

    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

    KIAA1191 Antibody (G-4) References:

    1. Familial adenomatous polyposis and mental retardation caused by a de novo chromosomal deletion at 5q15-q22: report of a case.  |  Finch, R., et al. 2005. Dis Colon Rectum. 48: 2148-52. PMID: 16228830
    2. Damage-induced ubiquitylation of human RNA polymerase II by the ubiquitin ligase Nedd4, but not Cockayne syndrome proteins or BRCA1.  |  Anindya, R., et al. 2007. Mol Cell. 28: 386-97. PMID: 17996703
    3. Haematological & molecular profile of acute myelogenous leukaemia in India.  |  Sazawal, S., et al. 2009. Indian J Med Res. 129: 256-61. PMID: 19491417
    4. Superior outcome with hypomethylating therapy in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome and chromosome 5 and 7 abnormalities.  |  Ravandi, F., et al. 2009. Cancer. 115: 5746-51. PMID: 19795507
    5. Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes.  |  Vera-Carbonell, A., et al. 2009. Am J Med Genet A. 149A: 2513-21. PMID: 19842199
    6. Characterizing the novel protein p33MONOX.  |  Mishra, M., et al. 2011. Mol Cell Biochem. 350: 127-34. PMID: 21153684
    7. Brain-Derived Neurotrophic Factor in Neonatal Seizures.  |  Sullivan, BJ. and Kadam, SD. 2021. Pediatr Neurol. 118: 35-39. PMID: 33773288
    8. The role of KIAA1191 in the necroptotic pathway of multiple myeloma.  |  Xu, Z., et al. 2022. Ann Hematol. 101: 359-367. PMID: 34989828
    9. Serum biomarkers in patients with drug-resistant epilepsy: a proteomics-based analysis.  |  Ma, M., et al. 2024. Front Neurol. 15: 1383023. PMID: 38585359
    10. The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.  |  Edwards, SJ., et al. 1997. Am J Hum Genet. 60: 515-24. PMID: 9042910
    11. Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins syndrome.  |  Crawford, MJ., et al. 1997. Mamm Genome. 8: 841-5. PMID: 9337397
    12. Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybrids.  |  McDaniel, LD., et al. 1997. Hum Mutat. 10: 317-21. PMID: 9338586

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    KIAA1191 Antibody (G-4)

    sc-398723
    200 µg/ml
    $316.00

    KIAA1191 (G-4) Neutralizing Peptide

    sc-398723 P
    100 µg/0.5 ml
    $68.00

    What application is the blocking peptide sc-398723 P appropriate for?

    Asked by: TinTin
    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 Nice Western Blot data of KIAA1191 expressionNice Western Blot data of KIAA1191 expression in non-transfected 293T, human KIAA1191 transfected 293T, H4, HeLa and K-562 whole cell lysates. -SCBT QC
    Date published: 2015-02-02
    Rated 5 out of 5 by from Satisfactory Western Blot data of KIAA1191Satisfactory Western Blot data of KIAA1191 expression in non-transfected and human KIAA1191 transfected 293T whole cell lysates. -SCBT QC
    Date published: 2014-10-24
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    KIAA1191 Antibody (G-4) is rated 5.0 out of 5 by 2.
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