| Host species | Rabbit |
|---|---|
| Clonality | Monoclonal |
| Clone number | E22 |
| Isotype | IgG |
| Carrier free | No |
| Reacts with | Human |
| Applications | WB, IHC-P, IP, ICC/IF, Flow Cyt (Intra) applications |
| Immunogen | The exact immunogen used to generate this antibody is proprietary information. |
| Specificity | The antibody should recognize both pro-form and p20 cleaved-form. The antibody does not cross-react with other Caspase family members. |
| Form | Liquid |
| Purification technique | Affinity purification Protein A |
| Storage buffer | pH: 7.2 - 7.4 Preservative: 0.01% Sodium azide Constituents: PBS, 50% Glycerol (glycerin, glycerine), 0.05% BSA |
| Shipped at conditions | Blue Ice |
| Appropriate short-term storage duration | 1-2 weeks |
| Appropriate short-term storage conditions | +4°C |
| Appropriate long-term storage conditions | -20°C |
| Aliquoting information | Upon delivery aliquot |
| Storage information | Avoid freeze / thaw cycle |
Answer:Yes. It recognizes the pro-form and a p20 cleaved form of caspase-7.
Answer:Human samples.
Answer:WB, IHC-P, ICC/IF, IP and intracellular flow cytometry in validated human material.
Anti-Caspase-7 Antibody [E22] is a rabbit monoclonal antibody for studying the executioner caspase-7 in human cell and tissue samples. Caspase-7 is produced as an inactive precursor and can be processed to active fragments during apoptosis. Clone E22 recognizes both the pro-form and a p20 cleaved form, allowing changes in protein processing to be assessed in Western blot experiments. The antibody is also suited to paraffin-section immunohistochemistry, immunofluorescence, immunoprecipitation and intracellular flow cytometry in validated human material. Select the assay format to match the experimental question: Western blot can resolve precursor and cleavage-related bands, while imaging provides cellular localization without reliably distinguishing protein forms by size. Include untreated controls and an apoptosis-induction condition when evaluating activation. Apply suitable fixation, permeabilization and antigen retrieval protocols before staining. Caspase-7 signal should not be conflated with caspase-3 activity, and species outside validated human samples require independent evaluation. Use a consistent analysis window to compare conditions.
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