Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes.
Ontology highlight
ABSTRACT: The importance of fluorescence light microscopy for understanding cellular and sub-cellular structures and functions is undeniable. However, the resolution is limited by light diffraction (~200-250 nm laterally, ~500-700 nm axially). Meanwhile, super-resolution microscopy, such as structured illumination microscopy (SIM), is being applied more and more to overcome this restriction. Instead, super-resolution by stimulated emission depletion (STED) microscopy achieving a resolution of ~50 nm laterally and ~130 nm axially has not yet frequently been applied in plant cell research due to the required specific sample preparation and stable dye staining. Single-molecule localization microscopy (SMLM) including photoactivated localization microscopy (PALM) has not yet been widely used, although t
SUBMITTER: Kubalova I
PROVIDER: S-EPMC7917581 | biostudies-literature | 2021 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA