PUBLICATION

Time-lapse imaging beyond the diffraction limit

Authors
Chitnis, A., Nogare, D.D.
ID
ZDB-PUB-180730-3
Date
2018
Source
Methods (San Diego, Calif.)   150: 32-41 (Other)
Registered Authors
Chitnis, Ajay
Keywords
none
MeSH Terms
  • Animals
  • Animals, Genetically Modified/growth & development
  • Embryonic Development*
  • Intravital Microscopy/instrumentation
  • Intravital Microscopy/methods*
  • Microscopy, Fluorescence/instrumentation
  • Microscopy, Fluorescence/methods
  • Models, Animal
  • Time-Lapse Imaging/instrumentation
  • Time-Lapse Imaging/methods*
  • Zebrafish/growth & development*
PubMed
30056120 Full text @ Methods
Abstract
The zebrafish, with its rapid external development, optical transparency, and the relative ease with which transgenic lines can be created, is rapidly becoming the model of choice for examining developmental processes via time-lapse microscopy. The recent proliferation of techniques for super-resolution imaging now allows for an unprecedented view of embryonic development at high spatial and temporal resolution in live tissues. This review examines both the theoretical basis and practical application of a number of established and emerging super-resolution microscopy techniques, focusing on their application in time-lapse imaging of live zebrafish embryos.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping