Sentence examples for mm were incubated from inspiring English sources

White prehierarchical follicles (1 8 mm) and fragments of theca and granulosa layers of the 3 largest yellow preovulatory follicles F3-F1 (22–35 mm) were incubated in a medium supplemented with T3 (0.10.1, 10 100 100, or 1000 ng/mL) or ovine luteinizing hormone (LH) (10 ng/mL) in combination with doses of T3 (10 10, and 100 ng/mL).

Peptides at the concentration of 10 mM were incubated with trypsin or chymotrypsin at 37 °C.

Peptides at the concentration of 10 mM were incubated with trypsin or chymotrypsin (0.2 mg/ml) at 37 °C.

Taurine, GABA, Glu, and Asp (5.0 mM) were incubated with MDA (5.0 mM) in 0.2 mM PBS (pH 7.4) at 37°C for 24 h.

For the transformation assays the respective compounds (initial reactant concentration: 0.1 mM) were incubated in a final volume of 50 ml in 500-ml flasks.

The mixture was separated at acidic pH through HPLC and fluorescence after amino acids (5.0 mM) were incubated with MDA (5.0 mM) in 0.2 M PBS, pH 7.4, at 37°C for 48 h.

Purified procaspase-3/9-His6 athehe final concentration of 3 mM was incubated with 800 µL ultracentrifuged cell-free preparation from immature oocytes for 30 min at room temperature.

Taurine or GABA (5.0 mM) was incubated with MDA (5.0 mM) in 0.2 mM PBS (pH 7.4) at 37°C for 24 h.

Each substrate (1 mM) was incubated with the enzyme (1 µM) in 10 mM phosphate buffer (pH 7.0) at 37°C for 24 h.

Each substrate (1 mM) was incubated with or without the enzyme (1 µM) in 10 mM phosphate buffer (pH 7.0) at 37°C for 24 h.

The tri(Asp) substrate (1 mM) was incubated with 1 µM or 200 nM PahZ1KP-2 at 37°C in 10 mM phosphate buffer (pH 7.0) For di(Asp s [(β-l-Asp - l-Asp) and (β-l-Asp - l-Asp)], the dimers (1 mM) were hydrolyzed at 10 µM PahZ1KP-2.