April 23rd, 2021
•The presented method enables visualization of fluorescently labeled cellular proteins with expansion microscopy leading to a resolution of 70 nm on a conventional microscope.
Videos relacionados
Method to Visualize and Analyze Membrane Interacting Proteins by Transmission Electron Microscopy
In Vitro Polymerization of F-actin on Early Endosomes
Imaging Amyloid Tissues Stained with Luminescent Conjugated Oligothiophenes by Hyperspectral Confocal Microscopy and Fluorescence Lifetime Imaging
Probing The Structure And Dynamics Of Nucleosomes Using Atomic Force Microscopy Imaging
Imaging of Extracellular Vesicles by Atomic Force Microscopy
Mitochondria and Endoplasmic Reticulum Imaging by Correlative Light and Volume Electron Microscopy
Production of Dynein and Kinesin Motor Ensembles on DNA Origami Nanostructures for Single Molecule Observation
Characterizing Cellular Proteins with In-cell Fast Photochemical Oxidation of Proteins
Transverse Sectioning of Mature Rice (Oryza sativa L.) Kernels for Scanning Electron Microscopy Imaging Using Pipette Tips as Immobilization Support
Analyzing the Interaction of Fluorescent-Labeled Proteins with Artificial Phospholipid Microvesicles using Quantitative Flow Cytometry
ACERCA DE JoVE
Copyright © 2024 MyJoVE Corporation. Todos los derechos reservados