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In the quantitative approach (DIGE), two protein samples are labeled with fluorescent dyes and when combined and separated on a 2D gel can be visualized by measuring the fluorescence showing whether a protein is up- or down regulated and for how much.
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The interrelations of molecular pathways were visualized by measuring the similarity among annotated gene functions by gene sharing.
Channel localization was visualized by measuring the green fluorescent signal from GFP fused to the N-termini of either WT or Bdel1.
The results were visualized by measuring the wound spaces.
Liver-stages were visualized by measuring luciferase activity of parasites (expressing luciferase under the eef1a promoter) in whole bodies of mice (Ploemen et al., 2009).
The ER Ca2+ content of intact single Wt, Atgl /– and FB1-treated Atgl /– macrophages was visualized by measuring the cytosolic Ca2+ elevation in response to ER Ca2+ release using the sarcoplasmic/ER Ca2+ ATPase (SERCA) inhibitor 2,5-di t-butyl-1,4-benzohydroquinone (BHQ) in Ca2+-free medium.
The model inputs giving rise to a large implausibility measure are then considered as unlikely to be appropriate representations of the physical state of the system, and these regions of the model input space can be visualized by projecting the implausibility measure into subspaces of the model inputs.
The variation in the output measures can be visualized by plotting the intensity of the output measures over two-dimensional slices of the parameter space.
Regional similarities are visualized by plotting a (alpha^{ k)}) measures, employment b and unemployment c on a US county map.
The wounded (denuded) area was visualized by fluorescein staining (Fig. 3A) and measured at regular interval to assess the healing progress.
PBT crystal lamellae were visualized by electron microscopy and the thickness and spacing were measured by X-ray scattering analysis.
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