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The microscopy data showed that the temperature of first nuclei detection was independent of the agitation speed.
Electron microscopy data showed them to have clear core-shell structures, with the FA encapsulated inside a CA shell.
Moreover, μ-CT, biomechanics, FTIR-ATR spectroscopy, and polarized light microscopy data showed regeneration using keratose was similar to an Infuse control.
Transmission electron microscopy data showed two-phase composite nanostructures consisting of a cobalt ferrite core surrounded by a barium titanate shell-like coating.
However, preliminary flow cytometry and confocal microscopy data showed that the SL siRNA formulation increased uptake of siRNA into vesicular compartments of HeLa-cells in a concentration-dependent manner that could be augmented by exogenuos sPLA2.
Here our fluorescence microscopy data showed that CdSe/ZnS quantum dots (QDs) with primary size of 12 nm were readily phagocytized into the food vacuoles of Tetrahymena thermophila in a time- and dose-dependent manner.
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Transmission electron microscopy data show that the particles diameter is 4 6 nm.
X-ray diffraction and electron microscopy data show that the nanocomposite powder microstructure is retained in the coating with no decomposition of the metastable quasicrystalline dispersoids to equilibrium crystalline phases.
Taken together, the immunofluorescence and immunoelectron microscopy data show that PLEKHA7 is localized at the AJ belt of epithelial cells.
Moreover, cryo-electron microscopy data show that Pab87 adopts the same octameric structure in solution (Figure 2D).
Twelve clones were selected for expression of the YPF-TetR protein using fluorescence microscopy (data shown only for clone 3 in Figure 3A).
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