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Slides were viewed using a Leica LEITZ DMRX epifluorecence microscope.
Samples were viewed using a field-emission scanning electron microscope (FE-SEM) (Carl Zeiss Auriga, Germany).
The bioluminescence color images were viewed using the living image software overlay (Xenogen).
The specimens were viewed using a Tecnai G2 transmission electron microscopy at 75 keV.
Cells were viewed using a 100× objective.
Samples were viewed using a Cambridge S360.
Phylograms were viewed using TreeView 1.6.6 [61.6.6
The resulting trees were viewed using TREEVIEW [20].
Cilia were viewed using an inverted microscope (Diphot; Nikon, UK).
Cells were viewed using a microscope (Axioscope, Carl Zeiss Inc).
Trees were viewed using Dendroscope [26] or ITOL [27].
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