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We have preliminary microscopy data using 6-carboxyfluorescein diacetate which supports this notion.
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In both tests, the fluorimetric assay showed high sensitivity and good agreement with previously reported data using microscopy.
In this work, we explore in depth the neural and mesodermal structures of the pygidium of P. dumerilii, with new descriptive data using electron microscopy and a number of molecular markers combined with confocal microscopy.
In the limit of stationary solutions, the numerical results are validated by direct flow visualizations and experimental data using confocal microscopy.
As definitive electron microscopic evidence is needed to precisely determine the subcellular localization of CB2-Rs, our transmission electron micrograph data using immunoelectron microscopy approach shows a high-resolution definition of hippocampal CB2-R localization at the ultrastructural level.
We could confirm our flow cytometry data using confocal microscopy where we could detect membrane-associated S100A8/A9 on PMNs, monocytes and pDCs but not on T cells, mDCs or B cells.
As it is known from previous reports and confirmed by our data using confocal microscopy, PANC-1 and MIA PaCa-2, differentially from CAPAN-2 and BxPC-3, show a more aggressive phenotype, particularly MIA PaCa-2 that have an higher tumorigenic potential [ 29, 26].
Data using live video microscopy suggest that an individual NK cell can make serial contacts with multiple targets and majority of contacts lead to lysis of target cells.
The first level of higher-order compaction is the 30 nm chromatin fiber for which several models have been created based on experimental data using cryogenic-electron microscopy (cryo-EM) and X-ray crystallography.
In our imaging data, using super-resolution microscopy, we confirmed that Crif1 is mainly located in MIM (Supplementary Figure 3); thus, the reduction in Crif1 levels might affect the stability of the OXPHOS system in MIM and the energy production required for cell survival.
Notably, our data using time-lapse microscopy provides only correlative evidence for mechanical coupling; we currently do not have experimental evidence for a signaling event that couples contractions to extension formation and would thus favor a simpler model of mechanical coupling.
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Justyna Jupowicz-Kozak
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