Agilent provides xCELLigence impedance-based, label-free, real time cell analysis system and NovoCyte flow cytometers.
Automated microscopy and Spatial Proteomics
Automated microscopy and image analysis
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Quantitative measurements of apoptosis using the ACEA NovoCyte Flow Cytometer
Feb 23, 2016
In order to demonstrate the flexibility and verstality of the NovoCyte system for assessment of apoptotic events, we show three di fferent assays that can measure apoptosis in response to staurosporine, a broad kinase inhibitor known to induce apoptosis in many cell types.
The fi rst assay uses Annexin V to bind exposed PS on cell membranes for labeling early apoptotic cells and the DNA binding dye, 7-AAD, for labeling late apoptotic cells.
The second assay makes use of the fl uorescent dye JC-1, to measure the loss of mitochondrial membrane potential in early apoptotic cells. JC-1 is cell permeable and aggregates inside mitochondria when membrane potential is maintained, emitting fluorescence in the PE channel.
The third assay quantifi es caspase activity. Probe molecules containing a cleavage site speci c for caspase 3 & 7 are added to cells. When cleaved by these activated caspases in early apoptotic cells, the probe molecules enter the nucleus, bind to DNA, and fluoresce. This enables the direct readout of activated caspases in cells.
Read the application note.
Related technologies: Conventional flow cytometry
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