HIGHLIGHTS
- who: Meggie Hudspith from the Electron microscopy and NanoSIMS Fixed tissue samples were processed and embedded as per Hudspith et_al [54]Semithin sections (, nm) were sectioned perpendicular to the sponge surface and transferred to silicon wafers, stained with uranyl acetate and lead citrate, and imaged with a Zeiss Sigma Field Emission Scanning Electron Microscope (SEM) at , kV at the Electron Microscopy Centre Amsterdam (EMCA). Regions of interest were imaged and digitally mapped for subsequent NanoSIMS analysis. Transmission electron microscope (TEM) and fluorescence images were also taken from a subset of samples (Fig. , have published the paper: Harnessing . . .
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