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In the preparation of the solution for electrospinning, we used a solution that contained PVP mixed with Mg(NO3 2 · 6H2O and Fe(NO3 3 · 9H2O.
The assembled unmodified and 2′-F A/C modified 3WJs (1 μM) were mixed with MG (2 μM) in binding buffer containing 100 mM KCl, 5 mM MgCl2, and 10 mM HEPES (pH 7.4) and incubated at room temperature for 30 min. The fluorescence was measured using a fluorospectrometer (Horiba Jobin Yvon; SPEX Fluolog-3), excited at 615 nm, and scanning from 625 to 800 nm for emission.
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This uniform composite was then mixed with magnesium (Mg, 99%) powder and mixed in a Fritsch planetary mill (Fritsch, Idar-Oberstein, Germany; 500 rpm) for 10 min.
Laboratory co-formulated tablets were prepared as follows; accurately weighed 5 mg CTZ, 25 mg PPA and 100 mg NMS are mixed with 15 mg lactose, 10 mg magnesium stearate, 15 mg maize starch and 20 mg talc.
In the present work, small amounts (up to 1 wt%) of WS2 nanotubes are mixed with Mg-alloy (AZ31) using melt-stirring process above 700 °C.
Portion of ten mg of the prepared ion associate complexes were thoroughly mixed with 190 mg PVC powder, 350 mg of DBS or DOP or NPOE and 5 ml THF in glass Petri dishes (5°Cm diameter).
For example, 10 mg of 10% GMO mixed with 90 mg of 0% GMO resulted in 100 mg of 1% GMO.
A total of 2 mg samples were mixed with 200 mg of KBr and then pressed into discs, respectively.
This enzyme binds to NTA-Ni column chromatography confirming the functionality of the histidine tag. 5 mg of eggPC mixed with 0.12 mg DOGS-NTA-Ni lipids were used to formulate 1 ml lipid suspension.
Column experiments were performed under various ionic strengths (0.0 0.9 mM) using 10 mg L− 1 of Cd2 + without kaolinite colloids and 10 mg L− 1 Cd2 + mixed with 100 mg L− 1 kaolinite colloids.
β-Carotene (2 mg) was dissolved in 10 mL of chloroform and mixed with 20 mg of linoleic acid and 200 mg of Tween 80 followed by chloroform removal under nitrogen.
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