STORM & Photonics Read the Story Request Info Please fill out the form and a product expert will reach out to you shortly. First Name * Last Name * Email * Organization * Phone (optional) -- Select an option -- -- Select an option --N/A ...
必应词典为您提供super-resolutionmicroscopy的释义,网络释义: 显微成像技术;超解析显微技术;超高解析度显微影像技术;
Self-inspired learning for denoising live-cell super-resolution microscopy SN2N, a Self-inspired Noise2Noise module, offers a versatile solution for volumetric time-lapse super-resolution imaging of live cells. SN2N uses self-supervised data generation and self-constrained learning for training with...
Structured illumination microscopy (SIMSuperresolutionFluorescence microscopy is a valuable toolbox to study cellular structures and dynamics spanning scales from the single molecule to the live animal. The spatial resolution that can be achieved with any light-based microscopy is however limited to about...
Super-resolution Microscopy in Plant Cell Imaging. Although the development of super-resolution microscopy methods dates back to 1994, relevant applications in plant cell imaging only started to emerge in 2010. Since then, the principal super-resolution methods, including structured-illu... G Komis,...
Super-resolution microscopy (SRM) bypasses the diffraction limit, a physical barrier that restricts the optical resolution to roughly 250 nm and was previously thought to be impenetrable. SRM techniques allow the visualization of subcellular organization with unprecedented detail, but also confront ...
Super-resolution microscopy (SRM) refers to any optical technique that is used for the purposes of resolving structures beyond the diffraction-limited resolution of conventional light microscopes.
Find out more about Leica super-resolution microscopy solutions and how they can empower you to visualize in fine detail subcellular structures and dynamics.
Super-resolution microscopy (SRM) describes a number of microscopy techniques that enable imaging of cellular structures at resolutions beyond the Abbe diffraction limit. Nano-Boosters, Nano-Labels, and Nano-Secondaries, which consist of Nanobodies conju
The limits of conventional light microscopy (“Abbe-Limit“) depend critically on the numerical aperture (NA) of the objective lens. Imaging at large working distances or a large field-of-view typically requires low NA objectives, thereby reducing the optical resolution to the multi micrometer ran...