Measuring cell viability is an incredibly important step across all applied cell biology, including cell line development for biotherapeutics and cell immunotherapy. However, traditional tools such as flow cytometry and hemocytometry struggle to differentiate between live cells and cell debris and other contaminants due to their workflows.

In this webinar, Dr. Bernardo Cordovez will show how high-throughput, backgrounded membrane imaging and fluorescence membrane microscopy enables the measurement of cell viability and foreign particle impurities quickly and accurately, in a single workflow. In addition, he details how these techniques can be used to find residual particulate contaminants such as expansion beads, cellular aggregates, and others in concentrated cell therapy solutions. Lastly, Dr. Cordovez will look at how these techniques can be deployed in cell line development of therapeutic proteins to identify protein and cell aggregation quickly and accurately.

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