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Chiastocheta larvae are specific to Trollius fruits, and cannot be reared on artificial medium under controlled laboratory conditions.
After sterilization with 50% (w/v) commercial bleach for 30 min with gentle shaking, rice seeds were germinated on a Murashige Skoog medium under controlled conditions (28 °C/25 °C day/night, 8-h photoperiod, and 78% relative humidity).
The seedlings were exposed to 0, 20, 50, 100, 200, 400 and 500 mg/L of CuONPs in semi-solid half strength Murashige and Skoog medium under controlled growth chamber conditions for 14 days.
Rice (Oryza sativa) seeds with T-DNA insertion in DXR gene, 1B-14224, and wild type segregants from this FST line germinated on Murashige Skoog (MS) medium under controlled conditions of 28 °C day/25 °C night temperatures, 8-h light/16-h dark cycle, and 78 % relative humidity after sterilization with 50%% (w/v) commercial bleach for 30 min with gentle shaking.
VCM, emulsifiers, and catalysts are metered into polymerization vessels wherein PVC is produced through a chemical reaction in an aqueous medium under controlled conditions of temperature and pressure.
One hundred milligrams of intact tissue was exposed to physiological concentrations of different H3-labeled compounds (Sigma-Aldrich), to explore the capability of these cells to metabolize these substances, in serum-free buffering medium under controlled temperature and atmosphere.
Similar(53)
The stock culture was maintained in Bristol medium (Starr and Zeikus 1987) under controlled laboratory conditions at a photon flux density of 40 µmol m−2 s−1 (photosynthetically active radiation), a photoperiod of 16:8 h (light:dark) and a temperature of 20 ± 2 °C.
C3H10T1/2 cells were cultured in adipogenic medium under control (non-mechanically stimulated) conditions and under oscillatory surface stretch with 10% amplitude and 0.01 Hz frequency for 6 h per day for up to 5 days.
The study of the reaction between Ca(OH 2 and SO2 has been performed in the medium temperature range (300 450°C) under controlled dehydration conditions.
Plants were grown on MS agar medium or on soil under controlled environmental conditions at 16 h light/8 h dark cycles.
The grafts were grown on 1.5% (w/v) agar plates with half-strength MS medium for nine days under controlled short day conditions.
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