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While the pH of buffer solution was adjusted to 5.0, G4 and C4 are formed and SWCNTs were dispersed.
In order to increase the viscous drag, the viscosity of the buffer solution was adjusted from 40 to 80 cP by adding a proper amount of sucrose.
The pH of the buffer solution was adjusted with 0.1 M NaOH in the range of 1.0 5.0 for further experimentation.
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In the case of nanoliposome suspension prepared using the citric acid buffer, the pH of the solution was adjusted to about 6.5 using 300 mM sodium bicarbonate buffer to make a gradient between the inside and outside of the nanoliposomes.
The pH value of reaction solution was adjusted by buffer solution; add a certain amount of Fe VI) into the reaction solution under the condition of magnetic stirring, take samples at scheduled time, and then add a small amount of 0.1 mol·L−1 sodium thiosulfate to terminate the reaction.
The pH of the solution was adjusted by borax boric acid buffer solution.
The pH of the solution was adjusted to 4 using buffer solution (pH 4) in order to control the surface potential of the graphene and the Li[Ni0.2Li0.2Mn0.6]O2 particles.
The solution was adjusted to 250 ml with distilled water and buffer (the buffer reagent was prepared using 7.56 g Tris-Hydroxymethyl-aminomethane dissolved in 50 ml distilled water, pH = 10.7).
Then the bacterial solution was adjusted by dilution into phosphate buffer to obtain ca. 5 × 105 viable cells/ml.
Bis(hydroxyethyl)aminotris(hydroxymethyl)methane, (BT) buffer (Fluka) was used and the pH of the solution was adjusted to 7.4 by addition of diluted HCl.
The supernatant was discarded and the pellets were resuspended in sterile phosphate buffer saline (PBS, pH 7.4) and the OD of the solution was adjusted to 0.50 0.48 nm.
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