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The FOL compounds were distributed into a 96 well plate with each well containing 7 10 individual compounds of dissimilar shape and dissolved in 20 µl of methanol at a concentration of 6 mM.
The compounds were distributed into 384-well source plates (BD Falcon Microtest™ from BD Biosciences, Le Pont De Claix, France), 20 μL per well at 100 μM final concentration diluted in print buffer (PB) (150 mM phosphate, 0.005% CHAPS pH 8.5).
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The compounds were distributed in sterile 96-microwell plates with a Sciclone ALH 3000 workstation (Caliper Life Sciences, Hopkinton, MA).
The compound was distributed into tissues rapidly and extensively after intravenous administration and was mainly distributed into the liver, heart and kidneys.
During the production of worldwide mostly used explosive compound – 2,4,6-trinitrotoluene its isomers were distributed into the environment.
The glands producing the compounds are distributed on various parts of the body.
Then the bacterial cells were diluted 10-fold in Mueller-Hinton broth and were distributed into 96-well microtiter plates, which were supplemented with compounds (12, 14 18, 24 26, 33, 35, 36) ranging from 128 to 0.25 μg mL−1.
Cells were distributed into 96-well plates, then dosed immediately with test chemicals in compound screening medium at 0.01, 0.1, 1, and 10 mg/l (n = 3) diluted from a 2A-DNT stock solution in dimethyl sulfoxide.
Aliquots of 2.5×10 cells were distributed into a 96-well plate in the presence of 100 10 μM of the different compounds for 4 h.
Forty-four male rats were distributed into 11 groups of four.
Four hundred eighty fingerlings were distributed into eight experimental groups.
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