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Fig1: Western blot analysis of Stat-1α/β on different cell lysates using anti-Stat-1α/β antibody at 1/500 dilution. Positive control:
Lane 1: Hela
Lane 2: NIH/3T3
Lane 3: MCF-7
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Fig2: ICC staining Stat-1α/β in HepG2 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig3: ICC staining Stat-1α/β in MCF-7 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig4: ICC staining Stat-1α/β in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig5: Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-Stat-1α/β antibody. Counter stained with hematoxylin.
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Fig6: Immunohistochemical analysis of paraffin-embedded mouse skeletal human kidney tissue using anti-Stat-1α/β antibody. Counter stained with hematoxylin.
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Fig7: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-Stat-1α/β antibody. Counter stained with hematoxylin.
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Fig8: Flow cytometric analysis of Hela cells with Stat-1α/β antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti rabbit IgG (FITC) was used as the secondary antibody.