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Single-molecule experiments have been carried out in our laboratory using imaging buffers containing glucose oxidase and catalase at the concentrations specified above, while the buffering agent, buffer strength, initial pH, flow chamber design, etc. are often varied to satisfy the needs of a specific experiment.
In addition to the buffer strength, the type of buffering agent, in particular its p Ka, and the desired solution pH are often varied in practice and may also play roles in modulating the acidification kinetics.
Cu release in acetate buffer could be further reduced by lowering the buffer strength to 10 mM (Figure 3B).
In contrast, the buffer strength depends on the amount of unopposed strong anion entering in the patient's circulation.
Optimal pH conditions were determined using a design of experiments method interrogating buffer strength, CO2% and device preparation conditions.
On the other hand, if the buffer strength is low, local alkalinity would lead to formation of bicarbonates and its direct reduction to formate.
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A solubility study at pH 7.4 and two buffer strengths (60 and 200 mM) was conducted on an indomethacin/saccharin cocrystal and compared to the γ-form of indomethacin.
The response curves are independent of buffer ionic strength.
In their research work, they efficiently improved the sensitivity of the SiNWs-FET sensor by optimization of qualities like gate voltage, probe concentration, and buffer ionic strength.
The extent of interaction can be modulated, in terms of size of the complexes, by choice of background buffer, ionic strength and polynucleotide length.
pH was measured immediately after sample collection at 25°C, using a Metrohm 704 pH-meter and a combination electrode (Metrohm) standardised against 2-amino-2-hydroxymethyl-1,3-propanediol 2-amino-2-hydroxymethyl-1,3-propanediol 2-amino-2-hydroxymethyl-1,3-propanediol 2-amino-2-hydroxymethyl-1,3-propanediol 2-amino-2-hydroxymethyl-1,3-propanediol 2-amino-2-hydroxymethyl-1,3-propanediol
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