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Morphology of deposits prepared by potentiostatic depositions was analyzed by scanning electron microscopy, and found to be different at high ultrasonic intensities.
The martensitic microstructures of NiTi shape memory alloys were examined by transmission electron microscopy and found to be self accommodating conglomerates of large primary (or first formed) plates and smaller secondary martensite plate clusters.
The martensitic microstructures of NiTi shape memory alloys were examined by transmission electron microscopy and found to be self accommodating conglomerates of large primary (or first formed) plates and smaller secondary martensite plate clusters.
In the case of SAMs of 3 the nature of this alteration was investigated via scanning tunnelling microscopy and found to presumably be caused by an order-disorder-transition.
The particle size results from unknown samples were compared to results from traditional size analysis by transmission electron microscopy, and found to have less than a 5% deviation in size for unknown product over the size range from 7 to 30 nm.
We performed a phagosome maturation test using confocal microscopy and found that SD treatment partially attenuated the phagosome arrest induced by M.tb infection.
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We study the surface morphology of the electrodes with scanning electron microscopy and atomic force microscopy, and find that the surface curvature and roughness can be reduced by optimizing the etching parameters.
The paper by Abbott et al. (2012) uses light microscopy and finds lower densities of inhibitory synapses than other studies using electron microscopy.
We characterized the surface potential of the TFA-derived perovskite film by Kelvin Probe Force Microscopy (KPFM), and found that the test results consist well with our suggested energy scheme.
The prepared NLCs were examined by differential scanning calorimetry (DSC), X-ray diffraction (XRD), and transmission electron microscopy (TEM) and found to have an imperfect crystalline lattice and a spherical morphology.
We examined the purified hDicer using negative staining transmission electronic microscopy (TEM) and found that the protein were mono-dispersed and homogenous in shape and dimension (Fig. 1D).
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