BacklinksExport to PDFBack to top Share via Share via... Twitter LinkedIn Facebook Pinterest Telegram WhatsApp Yammer Reddit TeamsRecent ChangesSend via e-MailPrintPermalink × Table of Contents Frequently asked Questions Lasers Detectors Microscopy MicroTime 200 Data Analysis all FAQs This is an old revision of the document! Frequently asked Questions Lasers The Intensity Response of my Laser is not linear Detectors The Dark Counts of my SPADs increased. When do I need to take action?Why do I not get the same count rates on both SPAD detectors? Microscopy MicroTime 200 Why do I not get the same count rates on both SPAD detectors? Data Analysis How can I analyze my data using non-PicoQuant software?NovaFLIM Calculated IRFNovaFLIM Licenses all FAQs How can I analyze my data using non-PicoQuant software?NovaFLIM Calculated IRFNovaFLIM LicensesThe Dark Counts of my SPADs increased. When do I need to take action?The Intensity Response of my Laser is not linearUsing Old Dongles for FluoFit and Older Versions of SymPhoTime (SymPhoTime 32) with Windows 10 or 11Why do I not get the same count rates on both SPAD detectors? Using old dongles for FluoFit and older versions of SymPhoTime (SymPhoTime 32) with Windows 10 or 11 faq.1741944875.txt.gz Last modified: 2025/03/14 09:34by doerr