Western blot (WB): | 1:500-2000 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Western blot analysis of Calpain 2/CAPN2 using anti-Calpain 2/CAPN2 antibody (BA1575). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: rat kidney tissue lysates,
Lane 5: rat lung tissue lysates,
Lane 6: mouse kidney tissue lysates,
Lane 7: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Calpain 2/CAPN2 antigen affinity purified polyclonal antibody (BA1575) 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 Calpain 2/CAPN2 at approximately 80 kDa. The expected band size for Calpain 2/CAPN2 is at 80 kDa.
IF analysis of Calpain 2/CAPN2 using anti-Calpain 2/CAPN2 antibody (BA1575).
Calpain 2/CAPN2 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-Calpain 2/CAPN2 Antibody (BA1575) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of U2OS cells using anti-Calpain 2/CAPN2 antibody (BA1575).
Overlay histogram showing U2OS cells stained with BA1575 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpain 2/CAPN2 Antibody (BA1575) 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 Calpain 2/CAPN2 using anti-Calpain 2/CAPN2 antibody (BA1575). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: rat kidney tissue lysates,
Lane 5: rat lung tissue lysates,
Lane 6: mouse kidney tissue lysates,
Lane 7: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Calpain 2/CAPN2 antigen affinity purified polyclonal antibody (BA1575) 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 Calpain 2/CAPN2 at approximately 80 kDa. The expected band size for Calpain 2/CAPN2 is at 80 kDa.
IF analysis of Calpain 2/CAPN2 using anti-Calpain 2/CAPN2 antibody (BA1575).
Calpain 2/CAPN2 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-Calpain 2/CAPN2 Antibody (BA1575) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of U2OS cells using anti-Calpain 2/CAPN2 antibody (BA1575).
Overlay histogram showing U2OS cells stained with BA1575 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpain 2/CAPN2 Antibody (BA1575) 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.