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T cells were treated with or without CCF52 ganglioside (15μg/ml) for 48hrs. Thereafter, cell lysates were subjected to analysis using the Proteome Profiler human apoptosis antibody array kit from R&D Systems (Minneapolis, MN) according to the manufacturer’s instructions. Arrays were developed with streptavidin-HRP for 30min on a rocking platform shaker. Developed signals were densitized using Image J software, pixel densities were normalized to untreated sample and expressed as mean pixel density. |
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Protocol tips |
T cells were treated with or without CCF52 ganglioside (15μg/ml) for 48hrs. Thereafter, cell lysates were subjected to analysis using the Proteome Profiler human apoptosis antibody array kit from R&D Systems (Minneapolis, MN) according to the manufacturer’s instructions. Arrays were developed with streptavidin-HRP for 30min on a rocking platform shaker. Developed signals were densitized using Image J software, pixel densities were normalized to untreated sample and expressed as mean pixel density. |
Publication protocol
T cells were treated with or without CCF52 ganglioside (15μg/ml) for 48hrs. Thereafter, cell lysates were subjected to analysis using the Proteome Profiler human apoptosis antibody array kit from R&D Systems (Minneapolis, MN) according to the manufacturer’s instructions. Arrays were developed with streptavidin-HRP for 30min on a rocking platform shaker. Developed signals were densitized using Image J software, pixel densities were normalized to untreated sample and expressed as mean pixel density.
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