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Stimuli were flashed for 33 ms using an intertrial interval of 5 s and a design that carefully balanced targets and distractors in a pseudo-random sequence.
Six electric pulses with the fixed pulse duration of 50 msec/pulse, were delivered at an interval of 200 ms using an electric pulse generator.
Series of images were captured at 250 frames per second with pixel number of 800 × 800 (exposure time is 3.97 ms) using an ORCA-Flash4.0 V2 C11440-22CU camera from Hamamatsu.
Purified proteins were analyzed by Matrix Assisted Laser Desorption Ionization (MALDI) Time of Flight (TOF) Mass Spectrometry (MS) using an Ettan MALDI-TOF Pro system (Amersham Biosciences).
Briefly, oligosaccharides in the hydrolysates were analysed by MALDI-TOF MS using an Autoflex III MALDI-TOF/TOF spectrometer (Bruker Daltonics, Bremen, Germany).
Analytes were then optically detected prior to MS using an ACQUITY FLR detector with excitation and emission wavelengths of 250 and 428 nm, respectively.
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Gold concentrations were quantified by inductively coupled plasma mass spectrometry (ICP-MS) using an Agilent 7500c system (Agilent. Tokyo, Japan).
The supernatant was then decanted and analyzed for total arsenic by ICP-MS using an X Series II ICP-MS (Thermo Scientific Inc., Waltham, MA, USA).
IMPROVE and MOUDI samples were analyzed using Panalytical XRF instruments using the IMPROVE protocol, then analyzed using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) using an Agilent 7500i.
Thus, ethylene polymerization was conducted in the presence of p-methylstyrene (p-MS) using an OMMT (organically modified MMT -intercalated MMT -intercalatedyst (Et[Ind]2ZrCl2 in cometalloceneith MAO), resulting in p-MS-catalystng PEt[MMT nanocomposInd]2ZrCl2
ESI-MS were measured on Ultimate 3000 LC-MS using an electrospray ionization method with negative mode.
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