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Using Fluorescence Methods to Improve Cell and Nuclei Counting Accuracy
Overview
This webinar will include a live demonstration and technical discussion of fluorescence methods for cell counting. Multiple sample types, including primary cells and isolated nuclei will be analyzed during the presentation.
Attendees will learn:
- How to select the optimum method for counting tissue culture, primary cells, and isolated nuclei
- The differences between brightfield and fluorescence imaging methods for cell counting and viability assessment
- How the CellDrop Automated Cell Counter removes plastic slides from the cell counting workflow
Duration:
The presentation will last approximately 30 minutes. Presenters and moderators will address questions during the demonstration. Additional time will be allotted for further questions when the presentation concludes.
Speaker Bio:
Dan Schieffer
Scientific Director
Scientific Director Dan Schieffer joined DeNovix in 2013. Dan holds a bachelor of science degree in biotechnology from the University of Delaware and a master’s degree in immunology from Villanova University. At Villanova, he developed a novel flow cytometry-based FRET system to study T-cell activation. Prior to joining DeNovix, Dan also held product development roles at NanoDrop technologies and was a research assistant at the University of Pennsylvania. At Penn, Dan’s investigations included high-throughput RNAi studies of viral pathogenesis in insects.
Dr. Carol Ajjan
GSS Equipment & Instruments Category Manager
Dr. Carol Ajjan is the Equipment and Instruments Category Manager at GSS. She received her BS in Chemistry and her Ph.D in Analytical Chemistry from George Mason University. During her doctoral research, Carol studied the binding of ciprofloxacin with surfactants, SDS and PFOS, using fluorescence spectroscopy.