Sentence examples for microscopy samples are from inspiring English sources

For most FRET measurements via fluorescence microscopy samples are fixed and mounted on cover slides.

For scanning electron microscopy, samples were critical-point dried (Hitachi HCP-2) and observed under a scanning electron microscope (Hitachi S-3000N).

In the case of the scanning microscopy, samples were filtered through 0.2 μm-pore-size acetone-resistant membranes (Millipore), fixed with 5% glutaraldehyde in 0.05 M cacodylate buffer (pH 7.2) for 60 min at room temperature and dehydrated in a graded series of ethanol and acetone.

For confocal microscopy, samples were analyzed using a Leica TCS SP2 confocal microscope.

For electron microscopy, samples were prepared as described in [58], and images were acquired on a FEI Morgagni 268 microscope.

For electron microscopy, samples were adsorbed to carbon-coated copper and negatively stained with 1% uranyl acetate.

For light microscopy, samples were fixed and embedded in Technovit 7100 resin (Kulzer, Wehrheim, Germany) as described [134].

For routine transmission electron microscopy, samples were fixed in 2.5% glutaraldehyde (v/v) and 5 mM CaCl2 in 0.1 M cacodylate buffer (pH 7.2).

Electron microscopy samples were prepared from exponential phase cultures by adding 2.1% final concentration of glutaraldehyde to 5 ml of culture in a Parafilm M foil-secured 14 ml Falcon polypropylene test tube (Becton Dickinson).

Histopathology and immunohistochemistry to detect CDV antigens in tissues were performed by published methods.[5] For electron microscopy, samples were selected from formalin-fixed paraffin-embedded small intestines that had evidence of hemoparasites occluding the small intestinal capillaries by light microscopy.

For transmission electron microscopy, samples were prepared as previously described [37].