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Fig1: Western blot analysis of ALP on different cell lysates using anti-ALP antibody at 1/1,000 dilution. Positive control:
Lane 1: Hela
Lane 2: HepG2
Lane 3: MG-63
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Fig2: ICC staining ALP in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig3: ICC staining ALP in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig4: ICC staining ALP in SW480 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 liver tissue using anti-ALP antibody. Counter stained with hematoxylin.
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Fig6: Immunohistochemical analysis of paraffin-embedded human liver cancer tissue using anti-ALP antibody. Counter stained with hematoxylin.
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Fig7: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ALP antibody. Counter stained with hematoxylin.
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Fig8: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-ALP antibody. Counter stained with hematoxylin.
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Fig9: Immunohistochemical analysis of paraffin-embedded mouse small intestine tissue using anti-ALP antibody. Counter stained with hematoxylin.
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Fig10: Flow cytometric analysis of Hela cells with ALP antibody at 1/50 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody