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Specimens for the analysis of stomach contents were injected with 37% formaldehyde solution into the stomach and were subsequently preserved in 10% formaldehyde solution.
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Consequently, tissue integrity was broken and damaged cells including their former content were injected into the peritoneal cavity.
The syringe content was injected into the SPE cartridge, and the procedure was repeated to transfer the entire sample.
To assess the flow cytometry assay under a wider range of tumour oxygen contents, mice were injected with hydralazine to reduce tumour blood flow, or allowed to breathe various gas mixtures during the 90 min exposure to pimonidazole.
But they do this at a lukewarm temperature, whereas the researchers wanted them to shrink specifically at 37C — body temperature — so that they'd squeeze their contents as soon as they were injected into the body.
The contents of the sample loop were injected automatically into an alumina capillary column (30 m × 0.550 mm).
Mice in group two were injected i.m. with 0.5 µg (based on HA content) HA and NA VLP in total 200 µl PBS for both prime and boost.
Samples were injected directly into the cuvette and excess sample was removed by repeatedly diluting the cuvette content in buffer.
Mice were injected Aβ25-35 Aβ25-35
Mice were injected intraperitoneally (i.p).
Sclerae were injected.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com