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Previously, the straw-bundled-like nanorods were synthesized in 1,4-butanediol using polyvinylpyrrolidone (PVP) as surfactant via refluxing polyol process for 30 min as reported by Zhang et al. [23].
Figure 6 shows that the slopes of two diagram indicate that the two materials show excellent adsorption rate at about first 30 min, which is desirable since catalyst's residence time in the regenerator of FCC process is very short (about 5 30 min), as reported in [16].
The InSb NWs were grown using the following layer sequence: first, InAs seed layer was grown at 550°C by simultaneously introducing TMIn (2×10−6 mole/min) and AsH3 (2×10−4 mole/min) into the reactor chamber for 2 min, as reported in previous work [10, 11]; then, the growth temperature was reduced to 440°C with only AsH3 flowing.
The optimal time for highest tumor/nontumor ratio is at 28 min as reported by [ 3].
The much larger activation observed with WT AMPK also declined between 10 and 60 min but was still evident at 60 min, as reported previously [18].
Through a midline incision, mild or severe ischaemia was induced by clamping the dissected bilateral renal arteries with non-traumatic microvascular clips (Kang Wei Medical Instrument Co). for 30 or 45 min as reported previously [ 22– 22].
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Most importantly, the kinetic coupling between 4/NHA decay and g 2.36 formation occurs with a strong solvent kinetic isotope effect (sKIE) (Table 4): sKIE(160 K)1 = τ1(D2O)/τ1(H2O) = 84 min/11 min ≈ 7.5 (85% D2O), as reported.
Primary mouse intestinal epithelial cells and adenoma cells were isolated from C57BL/6- Apc Min mice (Apc Min mice) as reported (Zhang et al., 2010).
After mixing, the mitochondria were first concentrated by centrifugation and incubated on ice for 30 min. As reported in the yeast cell-free mitochondrial fusion assay, this step helps to facilitate mitochondrial docking [ 5], thereby enhancing the reaction.
A portion of the Smc1-GFP barrel was photobleached by a 200 ms laser exposure, and fluorescence of the bleached area was measured at 15 s intervals for 8 min. As reported previously, Smc1-GFP fluorescence recovered little, if at all, during this period.
After 24 h, mice underwent 20 min MCAO as reported.
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