Sentence examples for pms control from inspiring English sources

8 μm pore-size tanswell filters(Costar, Corning Incorporated, U.S.A) were put in 24-well plate and the upper chambers were covered with BD Matrigel Matrix BD,U.S.A), then cells were seeded onto the filters at a concentration of 1 × 10 cells/well in 100 μL of FBS free medium with solvent without PMS (Control) or with different concentration of PMS or Catechin.

Plates were washed to remove floating cells and debris and then incubated with medium with solvent without PMS (Control) or with 200 μg/mL PMS or Catechin.

The fifth day after inoculation, mice were treated daily with solvent without PMS (Control) (n = 6) or with PMS (n = 6) at 200 mg/kg body weight by oral delivery.

For the colony formation assay, properly resuspend cells were randomly plated in 6-well plate at a density of 1 × 10 cells/well with solvent without PMS (Control) or with 100 μg/mL PMS or Catechin.

Cells were randomly plated in 6-well plate at a density of 2 × 10 cells/well with solvent without PMS (Control) or with 125 and 250 μg/mL PMS or with 100 and 200 μg/mL Catechin.

The study was designed as a 2 × 2 × 2 factorial arrangement of treatments: VW (low vs. high), PM (control vs. PP) and PI (0.75 vs. 0.85).

MSCR and HWTD results using the bio-additives with non-polymer modified binder show no improvements but when with a polymer modified (PM) binder, all additives show statistical improvements in resistance to rutting and stripping compared to a PM control.

The objectives of this study were to evaluate the effects of volume weight (VW; g/L), processing method (PM; control vs. precision processing [PP]), and processing index (PI; VW after rolling/VW before rolling) of barley grain on in situ ruminal kinetics and in vitro intestinal digestion.

For RNA interference, PIR cells were transfected with 50 pM control or MDM2 siRNA oligonucleotides (Dharmacon, ON-TARGETplus SMARTpool), with Dharmafect 2 (Dharmacon) according to the manufacturer's protocol.

Fifteen micrograms of fragmented cRNA was then added to a hybridisation cocktail (0.05 µg/µL fragmented cRNA, 50 pM control oligonucleotide B2, BioB, BioC, BioD, and cre hybridisation controls, 0.1 mg/mL herring sperm DNA, 0.5 mg/mL acetylated BSA, 100 mM MES, 1 M NaCl, 20 mM EDTA, 0.01% Tween 20) and cRNA was hybridised to chips.

A model carbon black particulate sample (M120) was selected for the negative PM control.