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At this peak of expression, a much brighter staining was assigned to ACTH-producing cells (Figure S1A, arrows).
Both reagents performed similarly, although once again the dextramer gave much brighter staining than the corresponding tetramer.
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Low staining intensity indicates normal fiber diameter, and bright staining intensity correlates with increased fiber diameter.
Staining patterns for this protein were much brighter in central regions than in the periphery.
Although JC-1 also produces green staining in regions in which it is less concentrated than in healthy mitochondria, the staining of dead cells by Sytox green was much brighter at the concentrations used.
In addition, the staining obtained with the IgM anti-p-p38 mAb was much brighter than that obtained with IgG monoclonal antibodies to p-p38 (data not shown), presumably because of the pentavalency of the IgM molecule.
The general pattern of results found in each series was very similar, showing very weak staining in the controls (A), slightly brighter staining in the I/R (B) and I/R+IPC (C) groups, and much stronger staining in the IPC group (D).
When the cocultures were stained for β1 integrin (Fig. 1B), the trophoblast cells showed a diffuse, punctate fluorescence that was much brighter than trophoblasts cultured in the absence of endothelial cells.
Now things are much brighter.
But this year looks much brighter.
The picture is much brighter today.
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