December 8th, 2021
•This protocol describes a method for morphometric analysis of neuromuscular junctions by combined confocal and STED microscopy that is used to quantify pathological changes in mouse models of SMA and ColQ-related CMS.
Video correlati
Spectral Confocal Imaging of Fluorescently tagged Nicotinic Receptors in Knock-in Mice with Chronic Nicotine Administration
Super-resolution Imaging of Neuronal Dense-core Vesicles
The Neuromuscular Junction: Measuring Synapse Size, Fragmentation and Changes in Synaptic Protein Density Using Confocal Fluorescence Microscopy
Protocol for Three-dimensional Confocal Morphometric Analysis of Astrocytes
Why Quantification Matters: Characterization of Phenotypes at the Drosophila Larval Neuromuscular Junction
Extracellular Recording of Neuronal Activity Combined with Microiontophoretic Application of Neuroactive Substances in Awake Mice
The Fibular Nerve Injury Method: A Reliable Assay to Identify and Test Factors That Repair Neuromuscular Junctions
Triggering Cell Stress and Death Using Conventional UV Laser Confocal Microscopy
Visualization and Live Imaging of Oligodendrocyte Organelles in Organotypic Brain Slices Using Adeno-associated Virus and Confocal Microscopy
Super-Resolution Imaging to Study Co-Localization of Proteins and Synaptic Markers in Primary Neurons