| Cross-sections were cut using an ultramicrotome and stained with safranin and light green. |
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| The sections were cut again using a Reichert ultramicrotome into 70-nm-thick sections. |
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| After resin polymerisation, the samples were cut using an ultramicrotome in 100 nm-thick slices. |
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| The SFTSV-infected Vero cell monolayer was fixed according to described methods and cut on ultramicrotome at 65 nm. |
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| Afterwards, the blocks were shaped as trapezes, having 1 mm on each side and then sliced into sections using an ultramicrotome. |
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| Thin sections were cut with an ultramicrotome and diamond knife and stained with lead citrate. |
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| Slices of 150 nm thicknesses were cut with an ultramicrotome. |
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| Specimens were thick sectioned for the presence of the archegonia and thin-sectioned with a diamond knife on an Ultracut-E ultramicrotome. |
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| Samples for transmission electron microscope analysis were prepared by cryocutting using an ultramicrotome prior to analysis. |
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| Blocks with specific areas were then chosen and sectioned with glass knives on a KBV ultramicrotome. |
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