The labelled cells were viewed using fluorescence microscopy, with appropriate filters.
Samples were viewed using the fluorescence microscope (Zeiss Axio-iM1ger M1) with the appropriate excitation/detection filters.
Slides were viewed using an Olympus AX70 fluorescence microscope equipped with appropriate filters (Olympus Optical Co., Hamburg, Germany).
Sections were viewed using an Olympus BX61 microscope equipped with the appropriate fluorescence filters and documented using the SIS software (SIS Olympus, Münster, Germany).
Specimens were viewed using a Leica microscope equipped with epifluorescence illumination and appropriate fluorescence filters for DAPI, Alexa Fluor 488/GFP and Alexa Fluor 546.
Slides were viewed using an Axiovert 200 (Zeiss, Germany) with filter sets appropriate for FITC, Rhodamine, and DAPI.
The parasites were viewed using a Zeiss Axioplan2 microscope equipped with a Plan-APOCHROMAT 100×/oil immersion lens and appropriate filters.
Slides were viewed using an Olympus BX-61 epifluorescence microscope equipped with a cooled CCD camera and appropriate filters.
Samples were viewed using a Cambridge S360.
Phylograms were viewed using TreeView 1.6.6 [61.6.6
