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These were 1 μm fluorescent beads (Fig. 2a) and a mouse intestine section (Fig. 2b).
These were 1μm fluorescent beads (Duke Scientific G0100) containing green fluorescing firefly dye and a fixed sample containing a mouse intestine section (Invitrogen fluo cells slide #4 F-24631).
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Figure 1 shows an example of these differences, using a fluorescently stained section of mouse intestine.
A 16 μm cryostat section of mouse intestine (specifically, the filamentous actin prevalent in the brush border) was stained with Alexa Fluor 568 phalloidin (FluoCells prepared slide #4 (F-24631), Invitrogen) and 50 μM gallium corrole solution [ 20].
To determine protein and gene expression in the intestine, section of the colon and small intestine from 8-week-old mice were rinsed with PBS and opened at the mesenteric border, and the epithelium was stripped of muscle using a glass slide.
In contrast to the mouse intestine, Drosophila ISCs failed to repopulate the gut after partial depletion.
A color-enhanced image of a mouse intestine showing ILC2-dependent mucus production.
Overlapping gene expression in fetal mouse intestine development and human colorectal cancer.
In addition, inactivation of a single Hmga2 allele in the mouse intestine epithelium significantly represses tumorigenesis driven by Lin28b.
Haramis, A.P. et al. De novo crypt formation and juvenile polyposis on BMP inhibition in mouse intestine.
Bando, J.K., Liang, H.E. & Locksley, R.M. Identification and distribution of developing innate lymphoid cells in the fetal mouse intestine.
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