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Labelled with fluorescein or peroxidase to permit visualization under light or fluorescence microscopy, were synthesized.
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The PEGylation reaction is shown in Scheme 1 B. First, oleylamine-coated USPIOs (5.5 ± 0.6 nm diameter by transmission electron microscopy (TEM)) were synthesized following a published method.
Gold and iron-containing nanoparticles were synthesized and characterized by scanning probe microscopy and transmission electron microscopy techniques.
ɑ-MoO3 micro-belts were synthesized via hydrothermal technique and characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), atomic force microscopy (AFM), energy dispersive X-ray analysis (EDX) and particle size analyzer.
The HD-PtNDs@AuNRs were synthesized by a seed-mediated growth approach and confirmed by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and UV vis spectroscopy.
These FA-CSNPs were synthesized using ionotropic gelation method and observed through field emission scanning electron microscopy (FESEM) and fluorescent microscopy.
For this purpose, spherical gold nanoparticles were synthesized and characterized with UV vis spectroscopy and transmission electron microscopy (TEM) analyses.
SWNT PNA SWNT conjugates were synthesized using carbodiimide coupling chemistry and characterized by host of techniques like scanning electron microscopy, atomic force microscopy and Fourier transform infrared spectroscopy.
Fe3O4@L-arginine nanoparticles were synthesized and characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and vibrating sample magnetometer.
The PLGA-based nanoparticles presented in this study were synthesized by emulsion evaporation method and characterized by transmission electron microscopy, dynamic light scattering, and energy dispersive spectroscopy.
The magnetic Fe3O4 nanoparticles were synthesized using co-sedimentation method, and their morphology was observed by scanning electron microscopy (SEM).
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