Please cite as: CSH Protocols; 2007; doi:10.1101/pdb.prot4816

This Protocol
Right arrow Full Text
Right arrow Update/discuss this protocolDiscussion icon
Right arrow Alert me when this protocol is cited
Right arrow Alert me when comments are published
Right arrow Alert me if a correction is posted
Services
Right arrow Similar protocols in this database
Right arrow Alert me to new releases of protocols
Right arrow Save to Personal Folders
Right arrow Download to citation manager
Right arrow Printer-friendly versionPrinter-friendly version
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Distel, M.
Right arrow Articles by Köster, R. W.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Distel, M.
Right arrow Articles by Köster, R. W.
Related Collections
Right arrow Zebrafish
Right arrow Developmental Biology
Right arrow Cell Imaging
Right arrow Imaging for Neuroscience
Right arrow Cell Biology, general
Right arrow Visualization
Right arrow Visualization, general
Right arrow Imaging/Microscopy, general
Right arrow Confocal Microscopy
Right arrow Imaging Development
Right arrow In Vivo Imaging
Right arrow In Vivo Imaging, general
Right arrow Light Microscopy
Right arrow Video Imaging / Time Lapse Imaging
Right arrow Laboratory Organisms, general
Right arrowRelated Protocol
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Legend icon

protocolProtocol

In Vivo Time-Lapse Imaging of Zebrafish Embryonic Development

Martin Distel and Reinhard W. Köster1

GSF--National Research Center for Environment and Health, Institute of Developmental Genetics, 85764 Neuherberg-Munich, Germany

1Corresponding author (reinhard.koester{at}gsf.de)


INTRODUCTION

Intravital time-lapse imaging is a powerful technique for investigating continuous developmental processes without missing crucial events. Because of the rapid embryogenesis, external development, and transparency of zebrafish embryos, their developmental processes can be visualized in time-lapse studies in the context of the living organism. The following protocol describes a method for performing intravital time-lapse imaging of zebrafish embryos over several days using confocal or compound stereomicroscopes.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Related Protocol

Construction of a Heated Incubation Chamber around a Microscope Stage for Time-Lapse Imaging
Paul M. Kulesa and Jennifer C. Kasemeier-Kulesa
CSH Protocols 2007: 4792. [Abstract] [Full Text]



This article has been cited by other articles:


Home page
CSHL ProtocolsHome page
K. Volkmann and R. W. Koster
In Vivo Retrograde Labeling of Neurons in the Zebrafish Embryo or Larva with Rhodamine Dextran
CSH Protocols, September 1, 2007; 2007(18): pdb.prot4832 - pdb.prot4832.
[Abstract] [Full Text]