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The benefits and limitations of each labeling process and specifically designed plastic label films are described.
Each labeling was measured at three different times, making three chromatographic separations.
The order of cell regions in each image is randomly generated for each labeling by each person.
Meanwhile, to remove any unbound antibody or QDs in above each labeling step, the cells were washed twice through employing FBS/PBS, in which the size of Ab or streptavidin-conjugated QD was about 25 nm, and the size of CD4 or CD8 or CD25 was about 1 5 nm, respectively.
Each labeling requirement has different specific wine making regulations and in order to label your wine as "Bordeaux," for instance, you have to abide by certain rules that go beyond which varietals are in the wine.
The ratios represent accumulated cell proliferation during each labeling period.
Tissues were washed in PBST (three times, 10 min per wash) between each labeling step.
This process yielded 8 12 final clusters for each labeling set.
Approximately 400 µg total RNA was used in each labeling reaction.
Sections were washed in PBS (three times, 10 min per wash) between each labeling step.
For each labeling set, fixed cells were labeled for 4 adhesion components (in addition to the stable expression of β3-integrin-GFP) as described in Table 1.
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CEO of Professional Science Editing for Scientists @ prosciediting.com