Anti-SOD1 Antibody

筛选器： All WB FCM

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  Western blot analysis of SOD1 using anti-SOD1 antibody (PB0453). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human Jurkat whole cell lysates,
  Lane 3: rat brain tissue lysates,
  Lane 4: rat spleen tissue lysates,
  Lane 5: mouse brain tissue lysates,
  Lane 6: mouse spleen tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SOD1 antigen affinity purified polyclonal antibody (PB0453) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for SOD1 at approximately 18 kDa. The expected band size for SOD1 is at 16 kDa.

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  Flow Cytometry analysis of A549 cells using anti-SOD1 antibody (PB0453).
  Overlay histogram showing A549 cells stained with PB0453 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SOD1 Antibody (PB0453) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

• 

  Western blot analysis of SOD1 using anti-SOD1 antibody (PB0453). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human Jurkat whole cell lysates,
  Lane 3: rat brain tissue lysates,
  Lane 4: rat spleen tissue lysates,
  Lane 5: mouse brain tissue lysates,
  Lane 6: mouse spleen tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SOD1 antigen affinity purified polyclonal antibody (PB0453) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for SOD1 at approximately 18 kDa. The expected band size for SOD1 is at 16 kDa.

• 

  Flow Cytometry analysis of A549 cells using anti-SOD1 antibody (PB0453).
  Overlay histogram showing A549 cells stained with PB0453 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SOD1 Antibody (PB0453) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.