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The samples (1 mg) were put into pH 5.0 PBS (3 mL).
Samples of mass in the range of 3 to 7 mg were put into aluminium crucibles, at a heating rate, β, of 5, 7, 10 and 12°C·min-1 up to a temperature of 500°C.
In this benzyl alcohol oxidation procedure, 5 ml benzyl alcohol (0.1 M in deionized water) and the catalyst (50 mg) were put in an autoclave reactor under vigorous stirring (around 700 rpm).
Other sieved portions were ground in an agate mortar; aliquots of 250 mg were put in 25 mL deionised water and treated in a Elmasonic S30H ultrasonic bath to extract soluble salts for the IC analysis.
In another article [ 22], herbal samples (approximately 50 mg) were put into 10-ml headspace vials, and the vials were capped with 20-mm magnetic crimp seal caps with PTFE/silicone septa.
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The samples weighed 50-mg were put into closed thermally fused melamine (TFM) digestion vessels whose span is 10 mL.
In a typical procedure, an appropriate amount of anhydrous hexachlorobutadiene (0.01 mol) and Mg (0.03 mol) were put into a glass-lined stainless steel autoclave of 50 ml capacity.
(R) N-[7(Methoxymethoxy chroman-2-yl]methyl 4-hydroxybenzyl aMethoxymethoxy chroman-2-yl]methyland 2–3 Methoxymethoxy chroman-2-yl]methyl
To determine the fraction of 15N and 13C incorporated in plant biomass, approximately 5 and 0.225 mg, respectively, were put into 5 × 8 mm tin cups in duplo.
About 1 mg bacteria were put in 800 μl 7H9 broth in a 2-ml test tube containing two 3 mm glass-beads.
Two replicate samples of approximately 50 mg of particles were put in the baskets.
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