Western Blot, Positive WB detected in: SH-SY5Y whole cell lysate (30ug), U-251MG whole cell lysate (30ug), Jurkat whole cell lysate (30ug), K562 whole cell lysate (30ug), HEK293 whole cell lysate (30ug), HEK293T whole cell lysate (30ug), SW620 whole cell lysate (30ug), All lanes: Parkin antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 52 kDa, Observed band size: 30 kDa, Exposure time: 2min
Immunofluorescence staining of A-549 cell with RAC08261 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
Overlay Peak curve showing 786-O cells stained with RAC08261 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.