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Using classical and confocal microscopy, we were able to compare the expression level of μ-opiate receptors and the influence of β-endorphin on transforming growth factor β type II receptor in organ culture.
Through phase-contrast microscopy, we were able to find elongated spermatids (data not shown).
Using transgenic animals and confocal microscopy, we were also able to study in detail various cellular aspects of regeneration.
Second, using fluorescence microscopy we were able to observe the translocation of two transcription factors to the nucleus during calcium and DTT treatment, in agreement with the T-profiler predictions.
Under fluorescent microscopy, we were able to confirm that the peptides were also present within the MI (Figure 2c), verifying that conjugating the peptide to the Ab allowed us to successfully target the peptide to the MI.
In this study, using fluorescence microscopy, scanning electron microscopy, and atomic force microscopy, we were able to compare and correlate microtubules and microfilaments with silica structure formed in diversely structured diatom species.
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As we continue to collect additional data on these receptors from orthogonal approaches, including nuclear magnetic resonance and electron microscopy, we are beginning to understand how these receptors interact with their ligands at the molecular level and how improving the pharmacology of GPCR signal transduction requires us to study these receptors using multiple biophysical techniques.
However, using both immunofluorescence and transmission electron microscopy (TEM), we were unable to find a junctional structure that correlated with spindle position.
Owing to sub-micron spatial resolution and the high sensitivity of the CARS microscopy technique we were able to resolve individual myofibrils.
By expressing a fluorescent TSPO fusion protein and using confocal microscopy, however, we were not able to detect the TSPO-containing fusion protein in the plasma membrane of MCs.
Using a combination of size-exclusion chromatography (SEC) and atomic force microscopy (AFM), we were able to determine the molecular mass and z-height of the AβO preferentially targeted by NU4.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com