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The chromatogram was produced using a UV Detector at 214 nm.
Gradient elution was performed using solvent A (1% aqueous acetic acid, v/v) and solvent B (100% acetonitrite); the gradient flow was as follows: 0 15 min with 14.5% B, 15 35 min with 14.6% B, 35 45 min with 100% B, and 45 60 min with 14.5% B. The flow rate was 1 mL/min, and HPLC chromatograms were obtained using a UV detector at 190 400 nm.
Detection was performed using a UV detector at 208 nm.
Docetaxel peaks were seen between 7 – 8 minutes using a UV detector set to 227 nm.
The data were acquired using a UV detector set at 325 nm.
The column effluent was detected using a UV detector at λmax of 227 nm.
Similar(36)
Detection of compounds was performed by using an UV detector at 210 nm for acetate and a refraction index (RI) detector for glucose.
Peak detection was performed using an UV detector set at 276 nm.
Glucose and cellobiose were detected using a Shodex RI-101 refractive index detector (Showa Denko, New York, NY, USA), while citric acid was detected using an UV detector at 210 nm (Dionex, Sunnyvale, CA, USA).
The peaks corresponding to glucose, xylose and arabinose were detected using a refractive index detector, whereas acetic acid and formic acid were detected using an UV detector set at 210 nm.
Ethanol, xylitol, glycerol, and acetic acid were detected with a refractive index detector Shodex RI-101 (Showa Denko, New York, NY, USA) while HMF and furfural were detected using an UV detector at 210 nm (Dionex).
More suggestions(15)
using a combination detector
using a point detector
using a frequency detector
using a prototype detector
using a conductivity detector
using a uv lift-off
using a decorrelating detector
using a uv lamp
using a uv imager
using a uv polymerization
using a repetition detector
using a uv transilluminator
using a uv assay
using a fluorescence detector
using a face detector
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