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The present study used high-resolution scanning electron microscopy to analyse the interaction of two small leucine-rich proteoglycans and several glycosaminoglycan chains with type I collagen fibrils obtained in vitro in a controlled, cell-free environment.
Ash suitability was evaluated using a number of conventional characterisation tools including XRF, calorimetric and microscopy to analyse solid phase distribution in relation to compositional differences derived from ternary diagram analogues.
We have two organic chemists who use gas chromatography-mass spectrometry and Fourier transform infrared microscopy to analyse the binding medium (such as linseed oil or egg yolk) that holds the pigment particles together to make a paint.
Therefore, we used this experimental system combined with confocal microscopy to analyse the localisation of Arabidopsis U1 snRNP- specific proteins, U1-70K, U1andnd U1C.
Here, we present a combined application of one-chromophore fluorescence lifetime microscopy and wavelength-selective fluorescence microscopy to analyse the function of a GFP fusion of the Brassinosteroid Insensitive 1 Receptor (BRI1-GFP) with high spatial and temporal resolution in living Arabidopsis cells in their tissue environment.
Four days later, we fixed the cells and used confocal microscopy to analyse spine number and size (Fig. 7b).
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We individually co-expressed the GFP-endophilin isoforms with mCherry-Lpd in HeLa cells and used TIRF microscopy to selectively analyse whether Lpd colocalizes with endophilin at the plasma membrane.
Electron probe microanalysis, scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction and optical microscopy were used to analyse deposited clads in terms of elemental composition, microstructure and flow characteristics in the deposition melt pool.
Surface 3D microscopy was used to analyse the resulting structure, to demonstrate a significant improvement in device flatness.
Analytical scanning electron microscopy was used to analyse residues in 111 features of 3 4000 micron conchoidal detachment diameter (Dco), examined on 23 solar cells.
X-ray diffraction and scanning electron microscopy were used to analyse the microstructure and identify the structural elements of the coatings.
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