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Recently, an efficient S-ABA production method was developed so that it could be used on crops, which led to the evaluation of different concentrations applied at or around veraison to colored table grapes.
Computational tests performed for four simple examples of electrochemical systems indicate that the most accurate results (close to the discontinuity) are obtained by combining the decomposition of the concentrations, applied at all discrete time levels, with the decomposition of the current.
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Hence, at the concentrations applied, SAHA and paclitaxel induced comparable cytotoxicity in the three cell lines tested.
Different ACh concentrations were applied at 2 min intervals in a random order and a standard concentration of ACh (∼EC20) was applied every third response in order to allow us to monitor for rundown.
It is also found that the transient response of the cell current is sensitive to oxygen concentration change at cathode/channel interface, whereas the current response is slow when step change of hydrogen concentration is applied at anode/channel interface.
In the arterial lumen, an open boundary condition for drug concentration was applied at the outlets and symmetry boundary conditions were applied at the flow centerline.
The model based on the AOB denitrification pathway can be used under the condition of a constant dissolved oxygen (DO) concentration, applied either at a low DO concentration (<∼0.5 mg O2/L) with any non-inhibitory nitrite (NO2−) concentrations or at higher DO (⩾∼0.5 mg O2/L) with relatively high NO2− (⩾∼1.0 mg N/L) but non-inhibitory concentrations.
Concentrations of Chlorpyrifos applied at different stages of growth of lettuce were examined at different time intervals of 1 h, 24 h and 7 days after pesticide application.
Studied factors included cryoprotectant type and concentration, freezing temperatures applied at different time periods and sublimation time.
To ensure a maximum response and to avoid potential fluctuation of the effective peptide concentration, Bk was applied at 8 µM.
By contrast, this same concentration of inhibitor applied at 2 dpf effectively reduced the cathepsin K activity in ML-II embryos to WT levels without an observed increase in developmental defects.
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