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The results of our simulation of closing the locking chamber are shown in Fig. 3.
The picture of the fabricated PDMS microfluidic channels with microchannel networks membrane (MCNM) and an enlarged microscopic image around the center chamber are shown in Fig. 2d.
The results of our simulation of opening the locking chamber are shown in Fig. 5: the graphs of the K@C601+ion displacement and change in the K@C601+ion kinetic energy in the locking chamber under the action of the electric field.
Results of the FDTD simulation are shown on figure 2, where the histogram of the SAR distribution in the whole media and at the bottom of the imaging chamber are shown.
Representative fluorescence micrographs of the cortical chamber are shown.
Data represent means; error bars represent standard deviations; n = 3. (B ) [ PSI + ]Weak HSP104GFP cells (SY2126) treated for 30 min at 40°C and imaged over time in a microfluidics chamber are shown.
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A schematic of the chamber is shown in Fig. 2a.
The layout of grouting boreholes in belt driving chamber is shown in Fig. 11.
The installation of the plastic membrane, containing the methane chamber is shown in Fig. 4.
The configuration of equipment in the chamber is shown in Fig. 6.
In a detonation test, the chamber was shown to contain an explosion equivalent to three grams of trinitrotoluene (TNT) without damage to the chamber.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com