STAU1 antibody

Cat.#: 115699

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Product Information

  • Product Name
    STAU1 antibody
  • Documents
  • Description
    STAU1 Rabbit Polyclonal antibody. Positive IP detected in mouse brain tissue. Positive WB detected in human brain tissue, K-562 cells, mouse brain tissue. Observed molecular weight by Western-blot: 55 kDa
  • Tested applications
    ELISA, WB, IP
  • Species reactivity
    Human,Mouse,Rat; other species not tested.
  • Alternative names
    FLJ25010 antibody; STAU antibody; STAU1 antibody
  • Isotype
    Rabbit IgG
  • Preparation
    This antibody was obtained by immunization of STAU1 recombinant protein (Accession Number: NM_001322930). Purification method: Antigen affinity purified.
  • Clonality
    Polyclonal
  • Formulation
    PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
  • Storage instructions
    Store at -20℃. DO NOT ALIQUOT
  • Applications

    Recommended Dilution:

    WB: 1:500-1:5000

    IP: 1:200-1:2000

  • Validations

    human brain tissue were subjected to SDS PAGE followed by western blot with Catalog No:115699(STAU1 antibody) at dilution of 1:300

    human brain tissue were subjected to SDS PAGE followed by western blot with Catalog No:115699(STAU1 antibody) at dilution of 1:300

    IP Result of anti-STAU1 (IP:Catalog No:115699, 4ug; Detection:Catalog No:115699 1:500) with mouse brain tissue lysate 3440ug.

    IP Result of anti-STAU1 (IP:Catalog No:115699, 4ug; Detection:Catalog No:115699 1:500) with mouse brain tissue lysate 3440ug.

  • Background
    Staufen1 (STAU1)-mediated mRNA decay (SMD) degrades translationally active mRNAs that bind the double-stranded (ds)RNA binding protein STAU1 within their 3'-untranslated regions (3'UTRs) [PMID:21307942]. STAU1 can binds to stem structures and protect Dvl2 mRNA from degradation by associating with the secondary structure in the U1 region which is located at 5′ position of second U stretch in the U2 region [PMID:17510634]. It has a role in specific positioning of mRNAs at given sites in the cell by cross-linking cytoskeletal and RNA components, and in stimulating their translation at the site.
  • References
    • Sugimoto Y, Vigilante A, Darbo E. hiCLIP reveals the in vivo atlas of mRNA secondary structures recognized by Staufen 1. Nature. 519(7544):491-4. 2015.
    • Alami NH, Smith RB, Carrasco MA. Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron. 81(3):536-43. 2014.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"