Eukaryotic cell flattening is valuable for improving microscopic observations, ranging from bright field to total internal reflection fluorescence microscopy. In this talk, we will discuss traditional overlay techniques, and more modern, microfluidic based flattening, which provides a greater level of control. We demonstrate these techniques on the social amoebae Dictyostelium discoideum, comparing the advantages and disadvantages of each method.
*This work was supported by the Deutsche Forschungsgemeinschaft (SPP 1128), the National Institutes for Health, and the Max Planck Gesellschaft.
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Authors
Albert Bae
MPI for Dynamics and Self-Organization, Goettingen and LASSP, Cornell University, Ithaca
LASSP, Cornell University, Ithaca and MPI for Dynamics and Self-Organization, Goettingen
LASSP, Cornell University, Ithaca and MPI for Dynamics and Selforganization, Goettingen
Christian Westendorf
MPI for Dynamics and Selforganization, Goettingen
Christoph Erlenkamper
Saarland University
Edouard Galland
Ecole Polytechnique
Carl Franck
LASSP, Cornell University, Ithaca
Eberhard Bodenschatz
Max Planck Institute for Dynamics and Self-Organization
MPI for Dynamics and Self-Organization, Goettingen and LASSP, Cornell University, Ithaca
LASSP, Cornell University, Ithaca and MPI for Dynamics and Self-Organization, Goettingen
LASSP, Cornell University, Ithaca and MPI for Dynamics and Selforganization, Goettingen
Carsten Beta
Institute for Physics and Astronomy, University of Potsdam and MPI for Dynamics and Selforganization, Goettingen