Sentence examples for mg were immersed from inspiring English sources

Firstly, the GCs (about 500 mg) were immersed into 5.65 mol/L hydrofluoric acid for 20 h to get rid off silicate glass host.

Cut pieces (6 mg) were immersed in a 2-ml solution (1 ml of 4% disodium hydrogen orthophosphate (w/v) and 1 ml of 0.5% TNBS (v/v)) and incubated at 40°C for 2 h.

The weighted samples of the polymeric matrices (about 35 mg) were immersed in PBS (phosphate buffer saline; pH 7.4).

A liver tissue sample (≈25 mg) were immersed in 1 mL cold Hank's balanced saline solution and disrupted with a tissue homogenizer for 30 sec on ice.

For RNA isolation, aliquots of approximately 100 mg were immersed in RNAlater® solution (Applied Biosystems, Foster City, CA) and stored at -20°C until use.

To obtain whole DNA from human brain tissue, tissue samples (50 250 mg) were immersed in 5 mL homogenization medium (0.32 M sucrose, 1 mM EDTA, 10 mM Tris HCl, pH 7.8) and disrupted with a glass Dounce-type homogenizer.

Pure Mg was immersed in saturated Mg(OH 2 solution, forming an Mg(OH 2 coated Mg surface.

The PVA nanofiber mat (0.5 mg) was immersed within the degassed aqueous solution of ferrous and ferric ions and stood for 1 h.

Carbon powder (Vulcan XC, 200 mg) was immersed in 1 M di-ammonium hydrogen phosphate solution and it was sonicated for an hour before stirring the same for 24 h at room temperature.

Nylon 6 nanofibers mat (1.5 mg) was immersed into 50 mL estrogen solution of a desired concentration in 100-mL glass conical flasks with cover, the solution was standing for 6 h to establish adsorption equilibrium kinetic experiments (0 to 6 h) and adsorption isotherm (initial concentration 0.1 to 2.0 mg/L), and thermodynamic studies (273 to 323 K) on adsorption were studied.

After weighing accurately by a digital balance with sensitivity of ±0.1 mg, the specimens were immersed in solution containing 1.0 M HCl solution with and without various concentrations of inhibitors.