Exact(12)
Indeed, our first experiments showed that living Hbt. salinarum cells can be stained in their growth medium using three MitoTracker dyes (MitoTracker Orange CMTMRos, MitoTracker Red-CMXRos, and MitoTracker Deep Red FM), as described in Materials and Methods and observed using a confocal fluorescence microscope (see Fig. 1).
Firstly we show the Drosophila can be stained in wholemount and this could aid rapid identification of drivers that are specific to the CNS or the PNS.
E.coli were stained using Syto9 to stain the nuclei and propidium iodide to detect damaged DNA, causing healthy cell to be stained in green whereas dying bacteria appear yellow (Fig. 4).
MSSA were stained using Syto9 to stain the nuclei and propidium iodide to detect damaged DNA, causing healthy cell to be stained in green whereas dying bacteria appear yellow (Fig. 1).
Alternatively, a recombinant protein or purified protein (or fragment thereof) may be stained in WB.
During the observation of the slides, the nucleus must be stained in pink or orange and the cytoplasm in blue [ 36].
Similar(47)
Cells in the superficial layer are stained red, while cells in the deep sublayer are stained in cyan (greenish-blue).
Cells in the superficial layer are stained red, while cells in the deep sublayer are stained in cyan (greenish-blue)(Credit: Nathan Danielson/Columbia's Zuckerman Institute).
The pneumococcal cultures were stained and examined under the microscope: living cells were stained in green, whereas dead cells were stained in red.
The cells' nuclei are stained in blue.
Viruses are stained in green; nuclei in blue (DAPI).
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