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Studies with extensively purified preparations demonstrated that the agent contains a protein that is required for infectivity.
The silver-alumina preparations demonstrated no reflections for bulk, metallic silver until the silver concentration was increased to 65% and calcined to 900°C.
Specifically, BNO 1095 extract preparations demonstrated specific binding to the dopamine D2 receptor [27, 28], which would thereby inhibit prolactin release from the pituitary gland and down-regulate a systemic hormonal cascade ultimately responsible for a wide range of menstrual symptoms in women suffering from PMS.
Western blot analysis of these preparations demonstrated the co-purification of Ozz and its direct interacting partner Elo C with the thin-thick filaments, indicating an association of the entire Ozz-E3 complex with fully assembled myosin (Fig. 5A).
Electron microscopy analyses of MVs preparations demonstrated the presence of vesicles with a diameter ranging from 100 nm to 1 µm, a size compatible with that described for MVs purified from other cells [23].
Immunoblots and quantitative analyses of these preparations demonstrated that ozz−/− and heterozygous pups had a significantly higher proportion of MyHCemb in the insoluble myosin fraction than their corresponding wild-type littermates (Fig. 6C and D).
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Improved drug deposition from liposomal preparations demonstrates its potential for dermal delivery.
Results with three herbal preparations demonstrate the utility of this novel approach to identify potential hazards and establish safe human use levels for botanicals in a cost efficient and informative manner that minimizes animal use.
Interestingly, after normalization for HIV-1 p24 content, no difference in infectivity was seen between these two viral preparations, demonstrating that the NA-mediated infectivity increase in influenza HA pseudoparticles is the consequence of NA activity on a substrate that is expressed at the surface of virions, rather that at the surface of target cells.
Cytospin preparations demonstrate distinct inflammatory cell morphology.
The localization of KDM2 enzymes to unmethylated DNA regions is consistent with mass spectrometry studies using nucleosome preparations, demonstrating enrichment at H3K9me3/unmethylated DNA nucleosomes [ 95].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com