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    KMT2E antibody

    Catalog Number: orb412434

    DispatchUsually dispatched within 5-10 working days
    $ 413.00
    Catalog Numberorb412434
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to KMT2E
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, IP, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenRecombinant full length protein of human MLL5
    Dilution rangeWB: 1:500-2000, IF/ICC: 1:50-200, IP: 1:50-100
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetKMT2E
    Entrez55904, 69188
    UniProt IDQ3UG20, Q8IZD2
    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-MLL5 antibody, anti-Histone-lysine N-methyltr
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    KMT2E antibody

    Western blot analysis of MLL5 expression in MCF7 (A), Hela (B), mouse lung (C), mouse brain (D) whole cell lysates. (Predicted band size: 68; 98; 131; 180-204 kD; Observed band size: 100 kD)

    KMT2E antibody

    Immunohistochemical analysis of MLL5 staining in rat ovary 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.

    KMT2E antibody

    Immunofluorescent analysis of MLL5 staining in U2OS 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 humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.

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