Sentence examples for ml were grown from inspiring English sources

For ubiquitination reactions, cultures of 50 ml were grown in LB medium, IPTG induction was for 2 h at 37 °C and the GST-fusion proteins were left on the glutathione-sepharose beads.

Axenic cultures (100 mL) were grown at 32°C with slow bubbling at 3.5% CO2 in air.

BY4247 and Δgcn5 cells (100 ml) were grown in YPD to OD600 = 1.0 and treated with Zymolase and pelleted.

Cultures of MRSA252 (100 ml) were grown to late exponential phase (OD600 = 3.0) and exposed to 0.1 mM linoleic acid or 0.1 mM hexadecenoic acid as described above.

Mating cultures (enough for 5.0 10.0 mL) were grown for at least 2.5 hours at 37°C in the presence of 50 µg/mL kanamycin until a density of 1.5×108 cells/mL was reached, as determined using a Petroff-Hausser counter.

Cultures (400 mL) were grown in 1 L Erlenmeyer flasks (Nalgene) in a 14∶10 light:dark cycle (ca. 250 µmol quanta m−2 s−1 photosynthetically active radiation) at 19°C, and the viruses amplified as outlined in Tai et al. (2003).

The multiple quantum wells with GaAs coverage of 10 ML are grown, instead of the fabrication of quantum rings using droplet epitaxy.

The temperature programme was: 150°C for 5 min and then 5°C/min to 300°C over 10 min. The A172 strain (100 ml) was grown in TSB.

For each protein, cell culture (100 ml) was grown overnight at 37°C with 50 mg/l ampicillin.

Thus, an overnight culture of 20 ml was grown at 37°C and diluted into two 1-l cultures to grow at 37°C till OD600 reached 0.6.

For each aspartic protease, an overnight culture (10 ml) was grown from inoculation of a recombinant E. coli BL21 DE3) colony in Luria-Bertani (LB) medium containing 50 μg/ml kanamycin (LBkan) with shaking (225 rpm) overnight at 37°C.