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Root samples were collected down to 1-m depth with the core method during 2005 and 2006, 40 and 114 days after sowing, in order to quantify their mass, length and diameter.
At the end of the experiment, cores were collected down to 1 m using a hydraulic corer.
Tumor and mucosa tissue samples were collected down to the serosa level at primary operation, snap frozen in liquid nitrogen and stored in-80°C until analysis.
The turves were collected down to the mineral horizon (depth of the soil organic horizon was 71 mm (3 142) and 54 mm (15 98), mean, minimum and maximum, at Thiisbukta and Solvatnet, respectively).
Mean ± SEM T = tumor tissue NM = Normal colon tissue Approx. TNM; A = T1, N0, M0; B = T2/T3, N0, M0; C = T2/T3/T4, N1/N2, M0; D = T2/T3/T4, N1/N2, M1 Tumor and normal colon tissue samples were collected down to the serosa layer during surgery and kept fresh frozen in liquid nitrogen and stored in -80°C until analysis.
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A 2.5-μm sharp-cut cyclone was attached upstream of the nephelometer, and PM2.5 for EC and OC was collected down-stream at a flow rate of 4 L/min.
Prior to implantation cells of five wells were collected, spun down at 300g for 30 seconds and supernatant was removed.
For preparation of total cell lysates, cells were collected, spun down and resuspended in sodium dodecyl sulfate-lysis buffer.
Fractions were collected, dried down under nitrogen stream and 4-MDDT resuspended in DMSO at 50 m M using its molecular mass as 413, as measured by GC-MS analysis (see below).
Per survival assay, 10 cells were collected, spun down, resuspended in 10 ml of selective medium (YP + 4% glucose + ethanol) and subjected to ethanol shock for 16 h (18 to 22% (v/ v)).
The stories that are best known today were collected and set down by enthusiasts like the Brothers Grimm, ETA Hoffman and Hans Christian Andersen.
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