Kinetic viability using PI
Determine the counts of PI-positive cells kinetically at 24, 48 and 72 hours
Determine the counts of PI-positive cells kinetically at 24, 48 and 72 hours
Perform endpoint viability assay on MDA-MB-231 and K562 cells treated with Benzethonium for 24, 48 and 72 hours
Measure Jurkat cell concentration and viability at titrations of concentrations and different mixture of cell viability, which can demonstrate the high-throughput capability of Celigo image cytometer
Drug treatment will increase the percentage of DRAQ7-positive cells over time
Perform endpoint viability assay on MDA-MB-231 and K562 cells treated with Benzethonium for 24, 48 and 72 hours
By measuring the number of Caspase 3/7 positive cells, we can determine the percent of apoptotic cells in the population
To image and count whole well populations of organoids in a rapid manner without having to take multiple, time consuming Z-stacked images
Monitor the effects of a panel of drugs on the apoptosis of U87MG Glioblastoma MCTS using Caspase 3/7 and Hoechst fluorescent staining
Image-based, automated analysis of 3-D tumor spheroids in microwell plates is becoming standard practice for the evaluation of anticancer drug compounds.
Monitor the effects of a panel of drugs on the invasion of U87MG Glioblastoma MCTS into Basement Membrane Extract (BME) Matrigel