Fluorophores accept light at a specific wavelength and re-emit it at a higher wavelength, giving each fluorophore an excitation and emission wavelength. Although there is a peak or maximal emission the range is often several hundred nanometers. This can cause problems where unwanted light enters several detectors giving false positives. Compensation is required to remove this unwanted fluorescence. Careful choice of fluorophores can reduce the amount of compensation needed.
The webinar is recommended to novices and researchers with limited experience of flow cytometry.
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Presented by: Dr Mike Blundell, Product Manager at Bio-Rad Laboratories
Mike Blundell graduated from the University of Edinburgh with a B.Sc. in Immunology. He then moved to University College London where he joined the group of Prof. Adrian Thrasher and obtained his Ph.D. His thesis research was focussed on the primary immunodeficiency Wiskott Aldrich Syndrome. He investigated novel activating mutations and developed lentiviral vectors for use in gene therapy treatments, some of which have now been used in clinical trials. Mike contributed to 50 peer reviewed papers and has now left academia to become a product manager for Flow Cytometry.
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