C9orf86 antibody

Cat.#: 108805

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Product Information

  • Product Name
    C9orf86 antibody
  • Documents
  • Description
    C9orf86 Rabbit Polyclonal antibody. Positive WB detected in MDA-MB-453s cells. Positive IF detected in HeLa cells. Observed molecular weight by Western-blot: 125 kDa
  • Tested applications
    ELISA, WB, IF
  • Species reactivity
    Human; other species not tested.
  • Alternative names
    bA216L13.9 antibody; C9orf86 antibody; FLJ10101 antibody; FLJ13045 antibody; Parf antibody; Partner of ARF antibody; pp8875 antibody; RBEL1 antibody
  • Isotype
    Rabbit IgG
  • Preparation
    This antibody was obtained by immunization of C9orf86 recombinant protein (Accession Number: BC002945). Purification method: Antigen affinity purified.
  • Clonality
    Polyclonal
  • Formulation
    PBS with 0.1% sodium azide and 50% glycerol pH 7.3.
  • Storage instructions
    Store at -20℃. DO NOT ALIQUOT
  • Applications

    Recommended Dilution:

    WB: 1:200-1:2000

    IF: 1:50-1:500

  • Validations

    MDA-MB-453s cells were subjected to SDS PAGE followed by western blot with Catalog No:108805(C9orf86 Antibody) at dilution of 1:600

    MDA-MB-453s cells were subjected to SDS PAGE followed by western blot with Catalog No:108805(C9orf86 Antibody) at dilution of 1:600

    Immunofluorescent analysis of (-20oc Ethanol) fixed HeLa cells using Catalog No:108805(C9orf86 Antibody) at dilution of 1:50 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)

    Immunofluorescent analysis of (-20oc Ethanol) fixed HeLa cells using Catalog No:108805(C9orf86 Antibody) at dilution of 1:50 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)

  • Background
    C9orf86, also known as RBEL1 (Rab-like protein 1), is a novel subfamily of GTPases within the Ras superfamily. It has two splice variants, RBEL1Aand RBEL1B. Unlike known Rabs that aremostly cytosolic, RBEL1B predominantly resides in the nucleus, whereas RBEL1A is localized primarily to the cytosol. C9orf86 is overexpressed in the majority of primary breast tumors, and knockdown of C9orf86 in MCF-7 breast cancer cells resulted in cell growth suppression associated with apoptosis [PMID: 23977139]. Western blot analysis revealed that the endogenous RBEL1 migrated at 110-125 kDa, 80 kDa, maybe due to a number of potential O-linked glycosylation sites.[PMID: 17962191]

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