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Immunogold labelling of cytoskeletons and handling of the probes for electron microscopy were done as described in detail elsewhere [37].
Membrane fractionation on 20 35% sucrose gradients and indirect immunofluorescence microscopy were done as described previously [22].
Higher magnification microscopy were done using AxioImager 21 microscope (Zeiss, Germany) as DIC, or in epifluorescence mode using excitation laser and filter cubes (Chroma Technology Corporation, USA) designed for either GFP (for green fluorescence sytox green) or Cy3 (for red fluorescence propidium iodide and Syto 59).
Scanning electron microscopy and transmission electron microscopy were done to describe the drug entrapped nanocapsules.
Bright-field, phase-contrast and dark-field microscopy were done on a Leitz DMRB (Leica, Solms, Germany) or an Axiovert 25 (Zeiss) microscope.
Table 4 summarizes the performance for culture methods in relation to smear microscopy.> -wrap-foot> Mycobacteridentificationsions on LJ were done basing on morphological features and Ziehl-Neelsen microscopy were done on doubtful colonies [ 15].
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Microscopy was done using an optical microscope (PUDA, China).
L.X., C.M.K. conducted the experiment with the assistance of Y.Z.C. Confocal microscopy was done by Y.W.W.
Scanning electron microscopy was done to understand the morphological and elemental information of silver nanoparticles.
Transmission electron microscopy was done using Philips EM028 transmission electron microscope.
Scanning electron microscopy was done to confirm the size and shape of silver nanoparticles.
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microscopy were plated
microscopy were confirmed
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microscopy were compared
microscopy were performed
microscopy were viewed
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