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To verify this, rectangular and sinusoidal nanostructures were fabricated and analyzed using force-distance curve measurements using atomic force microscopy and centrifugal detachment testing.
The process began with changing the surface properties on bacterial cells, as indicated in surface roughness measurements using atomic force microscopy, and holes then formed at the apical terminus of the cells.
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In this way, we simulate typical non-ideal conditions observed at nanoparticle measurement using atomic force microscopy.
These experiments involved the measurement, using atomic force microscopy, of interaction forces generated between Shewanella oneidensis MR-1 cells and single crystal growth faces of iron oxide minerals.
BPb was measured using atomic absorption spectrometry.
Here we describe force measurements, made using atomic force microscopy (AFM) and S. oneidensis MR-1 cells immobilized onto tip-less silicon nitride cantilever apices, to a series of flat single crystal iron oxide faces.
Additional measurements were performed using atomic force microscopy.
A multiscale approach was employed, combining tensile shear strength measurements, optical microscopy, and adhesion measurements at the nanoscale using atomic force microscopy.
The film thickness and microstructure was evaluated by surface imaging and RMS roughness measurements using an atomic force microscope (AFM) Asylum Research - MFP-3D in tapping mode.
The suspension was carefully collected for the measurement of Zn2+ concentration using atomic absorption spectrometry.
The measurement of cells elasticity using atomic force microscopy (AFM) indentation revealed that HS68 cells are significantly stiffer (p < 0.0001) than MCF10A and MDA-MB-231 cells.
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