The Infona portal uses cookies, i.e. strings of text saved by a browser on the user's device. The portal can access those files and use them to remember the user's data, such as their chosen settings (screen view, interface language, etc.), or their login data. By using the Infona portal the user accepts automatic saving and using this information for portal operation purposes. More information on the subject can be found in the Privacy Policy and Terms of Service. By closing this window the user confirms that they have read the information on cookie usage, and they accept the privacy policy and the way cookies are used by the portal. You can change the cookie settings in your browser.
The optical super-resolution technique DNA-PAINT (Point Accumulation Imaging in Nanoscale Topography) provides a flexible way to achieve imaging of nanoscale structures at ∼10-nanometer resolution. In DNA-PAINT, fluorescently labeled DNA “imager” strands bind transiently and with high specificity to complementary target “docking” strands anchored to the structure of interest. The localization of single...
Super resolution localization microscopy (SRLM) techniques such as STORM and PALM overcome the ∼200nm diffraction limit of conventional light microscopy by randomly activating separate fluorophores over time and computationally aggregating their nanometer resolution detected locations for image reconstruction. However, a basic limitation of current SRLM approaches for live cell imaging is their low...
Super-resolution localization microscopy (SRLM) is a new imaging modality that is capable of resolving cellular structures at nanometer resolution, providing unprecedented insight into biological processes. Each SRLM image is reconstructed from a time series of images of randomly activated fluorophores that are localized at nanometer resolution and represented by clusters of particles of varying spatial...
Localization-based super-resolution techniques are revolutionizing biological research by breaking the diffraction limit of fluorescence microscopy. Each super-resolution image is reconstructed from a time series of images of randomly activated fluorophores. Here, a fundamental question is to determine the minimal imaging length so that the reconstructed image faithfully reflects the biological structures...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.