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Anti-HER2 immunoliposomes bound efficiently to and internalized in HER2-overexpressing cells in vitro as determined by fluorescence microscopy, electron microscopy, and quantitative analysis of fluorescent probe delivery.
Qualitative (scanning electron microscopy) and quantitative (surface roughness test) measurements by Gupta et al. [22] also showed that the enamel after stripping with diamond disks and different polishing methods was significantly rougher than untreated control teeth.
Real-time bright-field microscopy and quantitative PMT detection indicated that that gram positive, gram negative and archaeal cells were effectively lyzed in a few seconds using the microfluidic chip protocol developed.
Many feebly magnetic phases like wustite, fayalite and clinoferrosilite appeared at higher temperature and reductant to feed ratios, which was confirmed by XRD, reflected light microscopy and quantitative mineralogical analysis.
They are well suited to live-cell microscopy and quantitative analysis, and they can be used in multiple imaging modes, including one- or two-photon fluorescence intensity or lifetime microscopy.
In this work, we address this problem by comparing diffusion parameters of a recently introduced model for water diffusion in brain matter to light microscopy and quantitative electron microscopy.
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The biological characteristics and changes of human DFCSs under the effect of TDM were studied with scanning electron microscopy, transmission electron microscopy, immunofluorescence microscopy, immunohistochemistry and quantitative real-time PCR.
The influence of the organoclay on the morphology of the hybrid was deeply investigated by means of wide-angle X-ray diffractometry, transmission and scanning electron microscopies and quantitative extraction experiments.
The SNARF-1-NP localization in endo/lysosomal compartments was confirmed by transmission electron microscopy (TEM) and quantitative co-localization analysis with fluorescent endolysosomal marker Rab-proteins by confocal laser scanning microscopy (CLSM).
Of 6 teeth of each group serial sections were cut and investigated with polarization light microscopy (PLM) and quantitative energy dispersive X-ray analysis (EDX).
Using negative stain transmission electron microscopy (TEM) and quantitative flow cytometry, we further demonstrate that mutations on key protein interfaces halt Snf7 assembly and block ESCRT function in vivo.
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