Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Figure 1. Western blot analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human SW579 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-Caspase 3/CASP3 (p17) antigen affinity purified monoclonal antibody (M00334-7) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for Caspase 3/CASP3 (p17) at approximately 35 kDa,(cleaved)20/17/12 kDa. The expected band size for Caspase 3/CASP3 (p17) is at 32 kDa.
Figure 2. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. Flow Cytometry analysis of HepG2 cells using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Overlay histogram showing HepG2 cells stained with M00334-7 (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 mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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.
Figure 5. IF analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in an immunocytochemical section of MCF-7 cells. The section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 1. Western blot analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human SW579 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-Caspase 3/CASP3 (p17) antigen affinity purified monoclonal antibody (M00334-7) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for Caspase 3/CASP3 (p17) at approximately 35 kDa,(cleaved)20/17/12 kDa. The expected band size for Caspase 3/CASP3 (p17) is at 32 kDa.
Figure 2. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. Flow Cytometry analysis of HepG2 cells using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Overlay histogram showing HepG2 cells stained with M00334-7 (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 mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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.
Figure 5. IF analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (M00334-7).
Caspase 3/CASP3 (p17) was detected in an immunocytochemical section of MCF-7 cells. The section was incubated with mouse anti-Caspase 3/CASP3 (p17) Antibody (M00334-7) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).