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Rat livers were weighed in a clean beaker.
After the black solution cooling down to room temperature naturally, 50 μL of OA, 50 μL of OAm, and absolute ethanol were added into the mixture to a total volume of 80 mL in a clean beaker.
The above-prepared UiO-66 powders (0.2 g) were placed into a clean beaker, which contained 200 mL of deionized water and mixed with appropriate amount of H2PdCl4 solution, and were vigorously stirred for another 1 h to disperse them completely.
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For measuring pH, 100 ml of the sample taken in a clean dry beaker stirred well until reached the stable value.
The plant water extracts were digested with 5 mL of concentrated HNO3 (Suprapure, Merck) and 2 mL of H2O2 (Suprapure, Merck) in a clean glass beaker and heated on a hot plate and diluted to 10 mL with double deionized water (Milli-Q Millipore 18.2 MW/cm resistivity).
The rats' livers were then removed and transferred to clean beaker and weighed.
Room temperature and hot water bath samples were placed in clean beakers with 100 and 250 ml milliQ water (i.e., 18 megaohms), respectively.
Third, the obtained homogeneous mixture was sonicated for 30 min after transferring them into a clean 10-ml beaker with the frequency of 20 kHz using ultrasonication bath.
After the heat shock, 30 synchronized larvae (based on the time of molting) from each group were placed into a clean 200 ml beaker with 150 ml distilled water and were fed the same amount of food.
An accurately weighed amount of the gel (0.1 g) was transferred into a clean dry 100 mL beaker and about 80 mL of ethanol was added.
In a typical SiFs preparation, a solution of silver nitrate (0.5 g in 60 ml of deionized water) was put in a clean 100 ml glass beaker.
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