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    EIF3L antibody

    Catalog Number: orb256511

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb256511
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to EIF3L
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Porcine, Primate, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human EIF3L. The exact sequence is proprietary.
    Dilution rangeWB: 1:500-1000, IHC-P: 1:100-200, IF/ICC: 1:100-500
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetEIF3L
    Entrez223691, 51386
    UniProt IDQ8QZY1, Q9Y262
    SourceRabbit
    StorageShipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
    Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    Alternative namesanti EIF3EIP antibody, anti EIF3S6IP antibody, ant
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    EIF3L antibody

    Western blot analysis of EIF3L expression in HEK293T (A), Hela (B), HGC27 (C), mouse kidney (D), rat kidney (E), rat testis (F) whole cell lysates. (Predicted band size: 66 kD; Observed band size: 67 kD)

    EIF3L antibody

    Immunohistochemical analysis of EIF3L staining in human Pancreas 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.

    EIF3L antibody

    Immunofluorescent analysis of EIF3L staining in HEK293 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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