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The basic scheme for the kinetic experiment is depicted in Figure 2 A. In these assays, a protein solution is mixed with a DNA solution containing the probe DNA (final concentration, 2.5 nM), nonspecific competitor DNA L, and quasi-specific competitor DNA LW, LS, or LT.
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The basic scheme for samples in reactions allows the addition of the amount of the substances in g (alternatively in mg or µg), in ml (or µl) or the definition of the used compound in mol (mmol) equivalents.
Thus, the basic scheme for selective elimination of meiosis-specific mRNAs in fission yeast seems to have many similarities to this bacterial system, except that the bacterial system represents a general degradation mechanism involving most mRNAs with no apparent strong sequence specificity for the mRNA target.
Figure 2 A basic scheme for NR-P-based assessment of blur.
Figure 4 A basic scheme for NR-P-based assessment of ringing.
Figure 7 A basic scheme for NR-P-based assessment of multiple artifacts.
Figure 5 A basic scheme for NR-P-based assessment of noise.
Figure 6 A basic scheme for NR-P-based assessment of temporal artifacts.
Figure 3 A basic scheme for NR-P-based assessment of blocking.
Figure 8 A basic scheme for NR-P-based assessment of visual quality using measures of various features.
Figure 10 A basic scheme for quality assessment methods based on hybrid of NR-P and NR-B-based approaches.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com