Cargando…
Overview of Single-Molecule Speckle (SiMS) Microscopy and Its Electroporation-Based Version with Efficient Labeling and Improved Spatiotemporal Resolution
Live-cell single-molecule imaging was introduced more than a decade ago, and has provided critical information on remodeling of the actin cytoskeleton, the motion of plasma membrane proteins, and dynamics of molecular motor proteins. Actin remodeling has been the best target for this approach becaus...
Autores principales: | Yamashiro, Sawako, Watanabe, Naoki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539652/ https://www.ncbi.nlm.nih.gov/pubmed/28684722 http://dx.doi.org/10.3390/s17071585 |
Ejemplares similares
-
An Infrared Actin Probe for Deep-Cell Electroporation-Based Single-Molecule Speckle (eSiMS) Microscopy
por: Yamashiro, Sawako, et al.
Publicado: (2017) -
Method for assessing the spatiotemporal resolution of structured illumination microscopy (SIM)
por: Boualam, Abderrahim, et al.
Publicado: (2021) -
New single-molecule speckle microscopy reveals modification of the retrograde actin flow by focal adhesions at nanometer scales
por: Yamashiro, Sawako, et al.
Publicado: (2014) -
siMS Score: Simple Method for Quantifying Metabolic Syndrome
por: Soldatovic, Ivan, et al.
Publicado: (2016) -
Compressive three-dimensional super-resolution microscopy with speckle-saturated fluorescence excitation
por: Pascucci, M., et al.
Publicado: (2019)