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    LCK antibody

    Catalog Number: orb338912

    DispatchUsually dispatched within 5-10 working days
    $ 413.00
    Catalog Numberorb338912
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to LCK
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human LCK. 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
    TargetLCK
    Entrez313050, 3932, 16818
    UniProt IDP06240, Q01621, P06239
    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 Tyrosine-protein kinase Lck antibody, anti Le
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    LCK antibody

    Western blot analysis of LCK expression in Hela (A), Jurkat (B), mouse kidney (C), rat liver (D) whole cell lysates. (Predicted band size: 58 kD; Observed band size: 56 kD)

    LCK antibody

    Immunohistochemical analysis of LCK staining in human lymph node 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.

    LCK antibody

    Immunofluorescent analysis of LCK 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. DAPI was used to stain the cell nuclei (blue).

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