Super-resolved microscopy techniques have overcome the diffraction limit to provide image resolutions approaching the scale of fluorescent labels. However, many of these techniques require significant experimental resources and expertise and impose long image data acquisition times, making it difficult to acquire super-resolved data from sufficiently large sample numbers to overcome intrinsic biological variation. We have worked to make stimulated emission depletion (STED) microscopy and single molecule localisation microscopy (SMLM) more straightforward to implement and more practical to image larger numbers of cells. Here we present work in progress developing easySLM STED and easySTORM, including a new modular microscope frame that we believe can make it easier to prototype microscopy techniques and to implement and maintain them in lower resourced settings.
Frederik Görlitz, Jonathan Lightley, Sunil Kumar, Edwin García, Ming Yan, Riccardo Wysoczanski, Yuriy Alexandrov, Jonathan Baker, Peter J Barnes, Ian Munro, Louise Donnelly, Christopher Dunsby, Mark A. A. Neil, Paul M. W. French
Jonathan Lightley, Frederik Görlitz, Somesh Kumar, Ranjan Kalita, Arinbjörn Kolbeinsson, Edwin García, Y.I. Alexandrov, Vicky Bousgouni, Riccardo Wysoczanski, Peter J Barnes, Louise Donnelly, Chris Bakal, Christopher Dunsby, Mark A. A. Neil, Seth Flaxman, Paul M. W. French
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