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    Anti-FRAT2 Antibody

    Catalog Number: orb1880749

    DispatchUsually dispatched within 5-10 working days
    $ 413.00
    Catalog Numberorb1880749
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to FRAT2
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the C-terminal region of human FRAT2. The exact sequence is proprietary.
    Dilution rangeWB (1/500 - 1/1000), IH (1/50 - 1/200), IF/IC (1/10 - 1/50)
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    Entrez23401
    UniProt IDO75474
    SourceRabbit
    StorageShipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
    Alternative namesGSK-3-binding protein FRAT2; Frequently rearranged
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    Anti-FRAT2 Antibody

    Western blot analysis of FRAT2 expression in human placenta (A), human heart (B) whole cell lysates. (Predicted band size: 24 kD; Observed band size: 23 kD)

    Anti-FRAT2 Antibody

    Immunohistochemical analysis of FRAT2 staining in human bladder carcinoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

    Anti-FRAT2 Antibody

    Immunofluorescent analysis of Anti-FRAT2 staining in ZR751 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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