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    MSH2 antibody

    Catalog Number: orb318988

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb318988
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to MSH2
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Primate, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human MSH2. The exact sequence is proprietary.
    Dilution rangeWB: 1:500-1:1000, IHC-P: 1:100-1:200, IF/ICC: 1:100-1:500
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetMSH2
    Entrez17685, 81709, 4436
    UniProt IDP54275, P43246, P43247
    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 DNA mismatch repair protein Msh2 antibody, an
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    MSH2 antibody

    Western blot analysis of MSH2 expression in Hela (A), A431 (B), NIH3T3 (C) whole cell lysates. (Predicted band size: 104 kD; Observed band size: 100 kD)

    MSH2 antibody

    Immunohistochemical analysis of MSH2 staining in human breast cancer 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.

    MSH2 antibody

    Immunofluorescent analysis of MSH2 staining in Hela 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.

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