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Exact(6)
hESC lysate for each time point (6 mg) was digested, followed by stable isotope dimethyl labeling, whereby the non-stimulated hESC (0 min) was labeled with light dimethyl labels, the 5 min time point with intermediate labels, and the 15 min time point with heavy dimethyl labels.
Genomic DNA (0.4 mg) was digested with HindIII (Promega) at 37°C overnight.
A portion of the frozen liver (120 150 mg) was digested in nitric acid.
PIM HS (∼50 mg) was digested using heparin lyase I distributively in a small volume and then separated by a gel filtration column.
A portion of the sample (155 mg) was digested with a mixture of 1 ml of concentrated HNO3, 0.1 ml of H2O2, and 0.25 ml of deionized distilled H2O.
Dry meconium (100 mg) was digested with a mixture of 1 mL 65% (v/v) HNO3 and 1 mL 30% (v/v) H2O2 in a water bath at 100°C for at least 5 h, and adjusted to a final volume of 5 mL with ultra-pure water.
Similar(54)
Samples of parchment (15 mg) were digested in a solution containing 15 mg CNBr dissolved in 1 ml formic acid (70%, w/v) at room temperature for 24 hours [22].
Soil samples (50 mg) were digested using the same protocol.
Samples of skin (100 to 200 mg) and cartilage (10 – 60 mg) were digested by shaking with 0.5 ml Proteinase K solution for 48 h at 55°C.
The cells pallets, homogenized tissues and organs (no more than 500 mg) were digested in a microwave (CEM MarsXpress Microwave Digester with Teflon microwave-safe vessels) before ICP analysis.
Thus, samples (1 mg) were digested with α-amylase (10 UI) and amyloglucosidase (20 UI) in 50 mM sodium acetate buffer (pH 5) at 55°C for 2 hours.
Related(20)
concentration was digested
ng was digested
mg was treated
mg was incorporated
mg was measured
mg was processed
ug was digested
mg was absorbed
patients was digested
concentrations was digested
mg was sandwiched
mg was used
mg was added
mg was started
mg was collected
mg was mixed
mg was isolated
mg was removed
mg was dissolved
mg was given
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