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Transmission electron microscopy experiments demonstrated nanoparticle aggregates and single particles in the cytoplasm.
Results from confocal laser scanning microscopy experiments demonstrated that this chemosensor was cell permeable and can be used as a fluorescent probe for monitoring Hg2+ in living cells.
Field emission scanning electron microscopy and tapping mode atomic force microscopy experiments demonstrated that relatively large micro-scale domain structures were exclusively found in the melt-polymerized polyurethanes.
Fluorescence microscopy experiments demonstrated that sensor 1 can be used as a fluorescent probe for the detection of Fe3+ in human liver cells (L-02) and rat neuronal cells (PC12).
Moreover, cell fractionation experiments and confocal fluorescence microscopy experiments demonstrated Bid cleavage and translocation of tBid from the cytosolic fraction to the mitochondria, which was blocked by treatment with a caspase-8 inhibitor.
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Supplementing crystalloid fluids with albumin also did not alter circulating neutrophil, monocyte, or lymphocyte counts, which suggests that systemic leukocyte recruitment is unaffected by albumin, and is consistent with the data from our intravital microscopy experiments demonstrating minimal effects of albumin on hepatic leukocyte recruitment.
Recent friction force microscopy (FFM) experiments demonstrated that it can be done mechanically by applying vibration to accessible elements of the system.
Importantly, fluorescence microscopy experiments further demonstrated that RBPY can be utilized as a fluorescent probe for the detection of Fe3+ in human liver (L-02) cells.
Both contain a number of tandem repeating homologous fibronectin type III (fnIII) domains, and atomic force microscopy experiments have demonstrated that the mechanical strength of these domains can vary significantly.
However, recent intravital microscopy experiments have demonstrated that the presence of Tregs in the lymph node (LN) decreases the frequency of stable contacts between self-reactive T cells and dendritic cells (DCs) that supposedly present the cognate antigen [9], [10].
Recently, multiphoton microscopy experiments have demonstrated that there are three stages in the process of in-vivo T cell activation and commitment to proliferation.
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