English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

In conventional scanning electron microscopy (SEM), granulocytes are difficult to distinguish from monocytes and lymphocytes. Therefore, we tried a new method of chilled SEM. Chilled SEM, a low-vacuum SEM with a cooling stage, provides images through back-scatter electrons. In comparison with specimens for conventional SEM, specimens for chilled SEM are not completely dehydrated in ethanol and require no criticalpoint drying and no metal coating. Chilled SEM images provide information beneath the surfaces of uncoated specimens. Thus, chilled SEM appears able to distinguish different leukocytes. Granules are observed in neutrophils, eosinophils, and basophils. Lymphocytes have no granules. Monocytes have well-developed ridge-like ruffles that other leukocytes do not.

The Surface Morphology of Normal Human Leukocytes by Chilled Scanning Electron Microscopy