WB
Western blot analysis of Calpain 1/CAPN1 using anti-Calpain 1/CAPN1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Jurkat whole cell lysates,
Lane 2: Hela whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: PC-3 whole cell lysates,
Lane 5: T47D whole cell lysates,
Lane 6: A549 whole cell lysates,
Lane 7: rat testis tissue lysates,
Lane 8: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Calpain 1/CAPN1 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate
IHC
IHC analysis of Calpain 1/CAPN1 using anti-Calpain 1/CAPN1 antibody.
Calpain 1/CAPN1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Calpain 1/CAPN1 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
ICC/IF
ICC/IF analysis of Calpain 1/CAPN1 using anti-Calpain 1/CAPN1 antibody.
Calpain 1/CAPN1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Calpain 1/CAPN1 Antibody at a dilution of 1:100. Fluoro594-conjugated Anti-rabbit IgG Secondary Antibody (red) was used as secondary antibody. The section was counterstained with DAPI (Blue).
FC
Flow cytometry analysis of PC-3 cell(1:100) Fluoro 488 conjugated goat anti-rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG Fluoro 488. Unlabelled sample (Red line).