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Fine powder was diluted in methanol to a methanolic concentration of 70% to give highest ion density inside the electrospray, without eliminating those neutrals which are highly water soluble.
Honey samples were dissolved in methanol to a final concentration of 0.03 g/mL.
Stock solutions of EDCs and NSAIDs dissolved in 50% methanol to a concentration of 100 mM were used as standards.
The stock solution of IS was dissolved in methanol to a final concentration of 1 µg/mL.
The standards for HPLC with diode-array detection (HPLC DAD) were dissolved in methanol to a concentration of 100 μg/ml and were stored at − 20 °C.
Then, the cells were harvested by centrifugation, suspended in 30 mL BMMY medium and induced for the expression of recombinant xylanase by adding methanol to a final concentration of 1.0% at 24 h intervals at 30 °C for 72 h.
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The QD methanol supernatant was diluted with methanol to an absorbance of about 0.2 (~0.01 g ml−1) at the 1S absorption peak (typically 850 nm), and used to prepare QD-sensitized mp-TiO2 films.
For each extract 1 g was weighed and dissolved in 5 ml of methanol to produce a solution with a concentration of 200 μg/μl.
They were dissolved in methanol to form a mixed solution with a designed doping ion concentration.
Individual trials were conducted using deionized water to represent an aqueous solvent and methanol to represent a polar organic solvent.
Mix the material in a test tube with about 2 mL of methanol to form a slurry.
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