Images
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Fig1:
This data was developed using HA750395, the same antibody clone in a different buffer formulation. Western blot analysis of MyoD1 on Hela cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA750395, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
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Fig2:
This data was developed using HA750395, the same antibody clone in a different buffer formulation. Flow cytometric analysis of MyoD1 was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (HA750395, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
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