Figure 1. Staining of cleaved (active) caspase 9 in HeLa cells treated with vehicle (0.1% DMSO in media) or with 1 ?M staurosporine for 4 hours. Cells were stained according to the kit protocol and
imaged using a Cellomics ArrayScan HCS Reader. Cells treated with stautosporine results in caspase 9 activation and an increase in staining.
The kit reagents have been optimized for use with the ArrayScan? HCS Reader and the Target Activation BioApplication Software Module, but they also can be used with other Cellomics BioApplication Modules. Thus, automated plate-handling, focusing, cell image acquisition/processing, and data analysis and management have been combined into a high-content screening (HCS) system to assay for test compounds affecting the activation of caspase 9. In addition to HCS instruments, cells labeled by the reagents in this kit can be viewed and analyzed by other fluorescence microscopes.
These kits allow direct in-cell measurements using a fixed end-point assay based on immunofluorescence detection in cells grown on standard high-density microplates. The primary antibody is
specific for human cleaved caspase 9 and does not cross-react with total caspase 9 or other caspases. The secondary antibody is conjugated to DyLight 549 Fluor (orange).
Product Detail
The Caspase 9 Activation Reagent Kits contain optimized reagents for the detection and quantitation of caspase 9 activation in cells.
The Caspase 9 Activation Reagent Kits contain optimized reagents for the detection and quantitation of caspase |
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