Flow cytometry and integrated imaging

Authors

  • V. Kachel Max-Planck-Institut für Biochemie
  • J. Wietzorrek Max-Planck-Institut für Biochemie

DOI:

https://doi.org/10.3989/scimar.2000.64n2247

Keywords:

flow cytometry, imaging, flash illumination, nanolite, LED-flash

Abstract


It is a serious problem to relate the results of a flow cytometric analysis of a marine sample to different species. Images of particles selectively triggered by the flow cytometric analysis and picked out from the flowing stream give a valuable additional information on the analyzed organisms. The technical principles and problems of triggered imaging in flow are discussed, as well as the positioning of the particles in the plane of focus, freezing the motion of the quickly moving objects and what kinds of light sources are suitable for pulsed illumination. The images have to be stored either by film or electronically. The features of camera targets and the memory requirements for storing the image data and the conditions for the triggering device are shown. A brief explanation of the features of three realized flow cytometric imaging (FCI) systems is given: the Macro Flow Planktometer built within the EUROMAR MAROPT project, the Imaging Module of the European Plankton Analysis System, supported by the MAST II EurOPA project and the most recently developed FLUVO VI universal flow cytometer including HBO 100- and laser excitation for fluorescence and scatter, Coulter sizing as well as bright field and and phase contrast FCI.

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Published

2000-06-30

How to Cite

1.
Kachel V, Wietzorrek J. Flow cytometry and integrated imaging. scimar [Internet]. 2000Jun.30 [cited 2021Jan.24];64(2):247-54. Available from: http://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/758

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Section

Articles