Exact(1)
On the other hand, the collision of the electron beams with the Mg substance on the top of the anode releases some magnesium ions to ablate which leads to reaction with the nitrogen ions triggered in each shot, then forms magnesium nitride which is deposited on the substrate.
Similar(59)
This means that after 8 days, you will have 20mg/2, or 10 mg of substance; after 16 days, you will have 10 mg/2 or 4 mg left of the substance; after 24 days, you will have 5 mg/2, or 2.5 mg left of the substance, and after 32 days, you will have 2.5 mg/2, or 1.25 mg left of the substance.
It requires approximately 5 mg of substance.
The standard drug (ciprofloxacin, 1 mg/mL of sterile distilled water), compounds 4a o (500 μg/mL in 10 % DMSO, prepared by dissolving 2.5 mg of substance in 5 mL of 10 % DMSO solution in water), and control sample (a 10%% solution of DMSO in water) were added to the respectively labelled 6 mm diameter wells.
After the net gas evolution in the test sample has come to an end (i.e. the degradation kinetic of the test sample and the control are more or less identical), a 2nd addition of another 200 – 800 mg active substance per liter is made to the test sample.
After the net gas evolution in the test sample has come to an end (i.e. the degradation kinetic of the test sample and the control are more or less identical), a second addition of another 200 to 800 mg active substance is made directly to the test system with gentle mixing.
In most cases, between 10 and 50 mg of substance was weighed out.
For the quinolones, 5 mg of each substance were dissolved into 10 mL of methanol.
The quantity of antimicrobial administered was converted to mg of active substance per kg of live weight.
About 5 mg of dried substance was placed in a TG furnace, and the analysis was conducted from 20 to 800 °C at a heating rate of 10 °C per min, under nitrogen.
In brief, fluorescein-isothiocyanate-inulin (Inulin-FITC; F3272-1; Sigma-Aldrich; St. Louis, MO, USA) and PAH (p-Aminohippuric acid sodium salt; A3759-25G; Sigma-Aldrich; St. Louis, MO, USA) (1 mg of each substance solved in 0.25 ml 0.9% NaCl) were applied (75 μl i.v ., followed by constant infusion of both substances (2 mg/ml inulin, 5 mg/ml PAH) with a rate of 3.7 μl/h/300 g BW.
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