Sentence examples for ml of experimental from inspiring English sources

Eggs were transferred to corresponding hatching baskets on the 18th day of incubation and received 0.5 ml of experimental solutions specific to each treatment.

mL−1 (for Sr2+) were exposed to 75 mM of CsCl or SrCl2 in 50 mL of experimental medium (LPM) at pH 7.5 and the soluble Cs+ or Sr2+ concentrations were assayed after specified time intervals.

Volumes of 200 μl to 2 ml of experimental blood samples (for laboratory assessment) were used for total DNA extraction.

Twenty-four hours after the culture, the medium was removed by aspiration and replaced with 1.5 ml of experimental medium containing 0, 10 100 100, 200, 400, and 600  μmol/l ATM.

Briefly, the second stage suspension cultures (25 mL) of all experimental organisms were added with racemic Carvedilol solution in methanol (0.01 mg/mL culture).

Experiments were carried out in 50 mL sterile polypropylene centrifuge tubes, into each of which was introduced 50 mL of sterile experimental growth medium and 100 μL of inoculant.

In this part of the study, 25 mL of the experimental solutions were placed in three polyethylene bags (Nasco WHIRL-PAK 2 OZ ., which were previously tested to be UV transparent.

Spawned sperms (200 μl) were added to 2 ml of the experimental medium each containing AgNPs at different concentrations (1, 2, 3, 4, and 5 nM) and kept for 30 min; 500 μl of this treated sperms from each concentration was pipetted into 2 ml of filtered seawater containing untreated eggs (50 eggs), mixed, and observed at intervals of 10 min under microscope.

Wells were incubated for 4 h at room temperature with 0.2 ml of either experimental samples (1 mg/ml total protein) or β3-Ig-6His standard, purified as described below, and diluted into DMEM with 10% FCS.

The medium was then removed, wells were washed once with phosphate buffered saline (PBS), and then 2 mL of fresh experimental medium (prepared as described above) was applied to begin the experiment.

OCSCs were dissociated and seeded into ultra-low attachment 6-well plates (Corning Incorporated, Corning, NY) containing 2 mL of fresh experimental stem cell medium (prepared as described above) at a density of 3×10 cells/well with a well surface area of 6.9 cm.