Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
(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 (PB9188). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Jurkat whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: rat thymus tissue lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse NIH/3T3 whole cell lysates,
Lane 6: mouse RAW264.7 whole cell lysates,
Lane 7: mouse ANA-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 3/CASP3 (p17) antigen affinity purified polyclonal antibody (PB9188) 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 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. Western blot analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Jurkat whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 3/CASP3 (p17) antigen affinity purified polyclonal antibody (PB9188) 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 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 3. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-Caspase 3/CASP3 (p17) Antibody (PB9188) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IF analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188).
Caspase 3/CASP3 (p17) was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Caspase 3/CASP3 (p17) Antibody (PB9188) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody.
Figure 1. Western blot analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Jurkat whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: rat thymus tissue lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse NIH/3T3 whole cell lysates,
Lane 6: mouse RAW264.7 whole cell lysates,
Lane 7: mouse ANA-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 3/CASP3 (p17) antigen affinity purified polyclonal antibody (PB9188) 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 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. Western blot analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Jurkat whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 3/CASP3 (p17) antigen affinity purified polyclonal antibody (PB9188) 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 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 3. IHC analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188).
Caspase 3/CASP3 (p17) was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-Caspase 3/CASP3 (p17) Antibody (PB9188) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IF analysis of Caspase 3/CASP3 (p17) using anti-Caspase 3/CASP3 (p17) antibody (PB9188).
Caspase 3/CASP3 (p17) was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Caspase 3/CASP3 (p17) Antibody (PB9188) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody.