Cleaved+pro Caspase-3 Recombinant Rabbit Monoclonal Antibody [PSH29-36]
cat.: HA752148
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse, Rat |
| Applications: | WB, IHC-P, FC(Intra) |
| Clonality: | Monoclonal |
| Clone number: | PSH29-36 |
| Form: | Liquid |
| Storage condition: | Store at 2-8℃. Avoid freeze. |
| Storage buffer: | PBS (pH7.4). |
| Concentration: | 0.5ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 32 kDa |
| Isotype: | IgG |
| Immunogen: | Recombinant protein within rat Caspase-3 aa 1-277. |
| Positive control: | HeLa (Human cervical adenocarcinoma cell) cell lysate, HeLa treated with 1μM staurosporine for 3 hours cell lysate, Jurkat (Human T-lymphoblastic cells) cell lysate, Jurkat treated with 1μM staurosporine for 3 hours cell lysate, C6 (Rat glioma cell) cell lysate, C6 treated with 1μM staurosporine for 3 hours cell lysate, NIH/3T3 (Mouse fibroblast) cell lysate, NIH/3T3 treated with 1μM staurosporine for 3 hours cell lysate, C2C12 (Mouse myoblast) cell lysate, C2C12 treated with 1μM staurosporine for 3 hours cell lysate. |
| Subcellular location: | Cytoplasm. |
| Uniprot #: | SwissProt: P42574 Human | P70677 Mouse | P55213 Rat |
| Alternative names: | Caspase3 A830040C14Rik Apopain CASP 3 CASP-3 CASP3 CASP3_HUMAN Casp3a Caspase 3 Caspase 3, apoptosis-related cysteine peptidase Caspase 3, apoptosis-related cysteine protease Caspase 3, apoptosis-related cysteine protease a Caspase-3 subunit p12 Caspase3 CC3 CPP 32 CPP-32 CPP32 CPP32B Cysteine protease CPP32 EC 3.4.22.56 ICE3 LICE mldy OTTHUMP00000165052 OTTHUMP00000165053 OTTHUMP00000165054 PARP cleavage protease Procaspase3 Protein Yama SCA 1 SCA-1 SCA1 SREBP cleavage activity 1 Yama Yama protein |
Images
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Fig1:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Western blot analysis of Cleaved+pro Caspase-3 on different lysates with Rabbit anti-Cleaved+pro Caspase-3 antibody (HA752148) at 1/2,000 dilution. Lane 1: HeLa (Human cervical adenocarcinoma cell) cell lysate Lane 2: HeLa treated with 1μM staurosporine for 3 hours cell lysate Lane 3: Jurkat (Human T-lymphoblastic cells) cell lysate Lane 4: Jurkat treated with 1μM staurosporine for 3 hours cell lysate Lane 5: C6 (Rat glioma cell) cell lysate Lane 6: C6 treated with 1μM staurosporine for 3 hours cell lysate Lysates/proteins at 15 µg/Lane. Exposure time: 10 seconds; ECL: K1801 Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: HA752148, 1/2,000 in primary antibody dilution buffer (K1803), overnight at 4 °C Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 32 kDa Observed band size: 32/17 kDa |
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Fig2:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Western blot analysis of Cleaved+pro Caspase-3 on different lysates with Rabbit anti-Cleaved+pro Caspase-3 antibody (HA752148) at 1/2,000 dilution. Lane 1: NIH/3T3 (Mouse fibroblast) cell lysate Lane 2: NIH/3T3 treated with 1μM staurosporine for 3 hours cell lysate Lane 3: C2C12 (Mouse myoblast) cell lysate Lane 4: C2C12 treated with 1μM staurosporine for 3 hours cell lysate Lysates/proteins at 15 µg/Lane. Exposure time: 25 seconds ; ECL: K1801 Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: HA752148, 1/2,000 in primary antibody dilution buffer (K1803), overnight at 4 °C Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 32 kDa Observed band size: 32/17 kDa |
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Fig3:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Application: Immunohistochemistry (IHC-P) Species: Mouse Tissue: Spleen Sample: Paraffin-embedded section Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C. Wash buffer: 1× TBST Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature. Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature. Primary antibody: HA752148, 1/10,000, 1 hour at room temperature. Secondary antibody: HA1119, 20 minutes at room temperature. |
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Fig4:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Application: Immunohistochemistry (IHC-P) Species: Mouse Tissue: Lymph node Sample: Paraffin-embedded section Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C. Wash buffer: 1× TBST Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature. Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature. Primary antibody: HA752148, 1/10,000, 1 hour at room temperature. Secondary antibody: HA1119, 20 minutes at room temperature. |
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Fig5:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Application: Immunohistochemistry (IHC-P) Species: Rat Tissue: Spleen Sample: Paraffin-embedded section Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C. Wash buffer: 1× TBST Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature. Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature. Primary antibody: HA752148, 1/10,000, 1 hour at room temperature. Secondary antibody: HA1119, 20 minutes at room temperature. |
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Fig6:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Application: Immunohistochemistry (IHC-P) Species: Rat Tissue: Lymph node Sample: Paraffin-embedded section Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C. Wash buffer: 1× TBST Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature. Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature. Primary antibody: HA752148, 1/10,000, 1 hour at room temperature. Secondary antibody: HA1119, 20 minutes at room temperature. |
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Fig7:
This data was developed using HA752148, the same antibody clone in a different buffer formulation. Application: Flow Cytometry (Intra) Species: Rat Sample: C6 (Rat glioma cell) Fixation: 4% Paraformaldehyde, 15 minutes at room temperature. Permeabilization: 0.1% Tween-20, 15 minutes at room temperature. Blocking: 1% BSA + 10% normal goat serum, 15 minutes at room temperature. Antibody dilution buffer: 1x PBS. Primary antibody: HA752148 (1/500, Red) compared with Rabbit IgG Isotype Control (HA722127, Green), 15 minutes at room temperature. Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 15 minutes at room temperature. |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.