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The confocal microscopy data suggest that, once internalized, the mannosylated and deglycosylated recombinant OVA proteins traffic into MHC class II-containing compartments.
In the present study, electron microscopy data suggest that, during exposure of the ventricular myocyte to 0.64T hypotonic solution (which gives a 40% increase in cell volume), membrane reserves come from both suface sarcolemma (open caveolae) and intracellular membrane (closed caveolae).
Whereas our immunoprecipitation and confocal laser scan microscopy data suggest that the phosphorylation of STAT3 is more prominent at Ser727 than at Tyr705, we cannot quantify the ratio of serine over tyrosine phosphorylated mitochondrial STAT3.
Crystal structures of independent sGC domains and homologues have been determined, and recent low-resolution electron microscopy data suggest how these domains might assemble in the full-length enzyme.
Fluorescence microscopy data suggest that because of the localisation of PpIX in the mitochondria, the primary cause of cell death after PDT is mitochondrial phototoxicity (Iinuma et al, 1994).
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Scanning electron microscopy data suggested that zinc oxide bacteria direct interactions may have damaging and breakdown of bacterial cell membranes [4].
Transmission electron microscopy data suggested that the synthesized graphene films are polycrystalline and its atomic arrangement is in short-range order.
Preliminary fluorescence microscopy data suggests that strain H16/pER2 (with expression of phaZ2 in trans) displayed a lower granule count than the wild type and the other overexpressing strains (data not shown).
Although the confocal microscopy data suggested that ESV cargo was released into the cytosol as a result of Bax expression, the fate of these organelles remained unclear.
Moreover, this distribution is in harmony with previous electron microscopy data suggesting that in Plasmodium the BB forms de novo after gametocyte activation (Sinden et al., 1976; 1978).
Taken together with the results from super-resolution fluorescence microscopy, these data suggest that by combining fluorescence microscopy modalities it may be possible to monitor Aβ on-cell aggregation on the single molecule level in real time.
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