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Fig1:Western blot analysis of UBC9 on different lysates with Rabbit anti-UBC9 antibody at 1/1,000 dilution.
Lane 1: HUVEC cell lysate,
Lane 2: HepG2 cell lysate,
Lane 3: HeLa cell lysate,
Lane 4: SH-SY5Y cell lysate,
Lane 5: U-937 cell lysate,
Lane 6: Jurkat cell lysate,
Lane 7: NIH/3T3 cell lysate,
Lane 8: PC-12 cell lysate,
Lysates/proteins at 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 1/1,000 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 UBC9 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 UBC9 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: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-UBC9 antibody. Counter stained with hematoxylin.
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Fig5: Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-UBC9 antibody. Counter stained with hematoxylin.