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For phosphorylation site identification, the purified LRRK2 protein was digested in-gel using various proteases and the resulting proteolytic peptides were analyzed by multiple mass spectrometer methods including MALDI-QqTOF, MALDI-ion trap (LCQ DECA XP), and nano-HPLC/ velos LTQ Orbitrap.
The collection and storage of serum samples and the UPLC and mass spectrometer methods applied have been previously described (Dunn et al., 2008; Zelena et al., 2009).
Apatinib concentrations in plasma were determined using fully validated specific liquid chromatograph/tandem mass spectrometer methods, with a lower limit of quantitation of 1.6 ng/ml.
Real-time PCR and matrix-assisted laser desorption-ionization time-of-flight mass spectrometer methods were employed for identification of presumptive pathogens.
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The mass of recombinant CTGF and NOV were determined with the MALDI-TOF/TOF mass spectrometer method (ultrafleXtreme MALDI-TOF/TOF mass spectrometer, Bruker Daltonics, Bremen, Germany).
These MRM/SRM transitions along with their retention times are exported as a tab-delimited file (tsv) and then used to populate a targeted mass spectrometer method file.
A programmed temperature gas chromatography-mass spectrometer method was designed to detect the released gases from the core at temperature 50 °C-290 °C-290 °C
Plasma DEX concentrations were measured using a gas chromotographic-mass spectrometer method (Oneida Research Services Inc, Whitesboro, NY, USA).
Uncalibrated radiocarbon ages are experimentally determined either by radiometric (often termed classical) or accelerator mass spectrometer (AMS) methods and are referred to as conventional ages.
Even for the same mass spectrometer, experimental methods yielded considerable changes in performance.
Recent improvements in injection techniques and mass spectrometer ionization methods have led to a variety of options to determine PBDEs in environmental samples.
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