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Fig1:Western blot analysis of p16 ARC on different lysates with Rabbit anti-p16 ARC antibody at 1/5,000 dilution.
Lane 1: HeLa cell lysate (15 µg/Lane),
Lane 2: MCF7 cell lysate (15 µg/Lane),
Lane 3: HepG2 cell lysate (15 µg/Lane),
Lane 4: Human brain tissue lysate (20 µg/Lane),
Lane 5: Mouse brain tissue lysate (20 µg/Lane),
Lane 6: Rat brain tissue lysate (20 µg/Lane),
Exposure time: 3 minutes;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.
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Fig2: ICC staining p16 ARC in N2A 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: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-p16 ARC antibody. Counter stained with hematoxylin.
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Fig4: Immunohistochemical analysis of paraffin-embedded mouse lung tissue using anti-p16 ARC antibody. Counter stained with hematoxylin.
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Fig5: Immunohistochemical analysis of paraffin-embedded rat spleen tissue with Rabbit anti-ARPC5 / p16 ARC antibody at 1/1,000 dilution.
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Fig6: Flow cytometric analysis of SH-SY-5Y cells with p16 ARC 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.