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Fig1: Western blot analysis of GRP78 on different lysates using anti-GRP78 antibody at 1/500 dilution.
Positive control:
Lane1: Mouse liver tissue
Lane2: Rat liver tissue
Lane3: HepG2
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Fig2: ICC staining GRP78 in A431 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 GRP78 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 GRP78 in HUVEC 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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Fig5: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-GRP78 antibody. Counter stained with hematoxylin.
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Fig6: Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-GRP78 antibody. Counter stained with hematoxylin.
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Fig7: Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue using anti-GRP78 antibody. Counter stained with hematoxylin.
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Fig8: Immunohistochemical analysis of paraffin-embedded human placenta tissue using anti-GRP78 antibody. Counter stained with hematoxylin.
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Fig9: Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue using anti-GRP78 antibody. Counter stained with hematoxylin.
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Fig10: Flow cytometric analysis of Jurkat cells with GRP78 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated Goat anti rabbit IgG was used as the secondary antibody.