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    HSP90B1 antibody

    Catalog Number: orb214702

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb214702
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to HSP90B1
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human GRP94. 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
    TargetHSP90B1
    Entrez7184
    UniProt IDP14625
    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 GRP94 antibody, anti TRA1 antibody, anti Endo
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    HSP90B1 antibody

    Western blot analysis of GRP94 expression in K562 (A), A549 (B), SP20 (C), PMVEC (D) whole cell lysates. (Predicted band size: 92 kD; Observed band size: 100 kD)

    HSP90B1 antibody

    Immunohistochemical analysis of GRP94 staining in human brain 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.

    HSP90B1 antibody

    Immunofluorescent analysis of GRP94 staining in NIH3T3 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. DAPI was used to stain the cell nuclei (blue).

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