Sentence examples for cytoplasmic particles from inspiring English sources

THE separation of cytoplasmic particles into fractions by differential centrifugation has been extensively used for the study of the distribution of intracellular cell constituents.

Instead, the regulated mRNAs are present in numerous very small cytoplasmic particles.

All antibodies gave similar results, with the exception of 2G, which also stains cytoplasmic particles previously described as possible artifacts [34].

Since our focus was to witness HSV1-APP interactions in out-going cytoplasmic particles through immuno-staining and dynamic imaging, we concluded that reliance on gD expression or human serum to block re-infection was inadequate.

While producing some artifacts, these methods have been profoundly successful, filling our textbooks with information about the structure and positions of cell walls, internal membranes, cytoskeletal filaments, and even large cytoplasmic particles like ribosomes.

By contrast, Tud and GFP-Vas were found to essentially co-localize in the nuage at distinct developmental stages (Fig. 5A C) whereas Tud remained undetected in the cytoplasmic particles containing Vas (Fig. 5A, lower panels).

We reasoned therefore that any particular cytoplasmic particle, even at later time points, in a cell with >30 particles in the cytoplasm has >90% chance of being out-going when cells are infected during a one-hour time window according to this synchronous infection protocol.

Cytoplasmic viral particles and electron-dense intracytoplasmic particles (dense bodies) were also clearly visible at 3 dpi in TB40/E-infected HCECs (figure 4C, D).

In contrast, cells transfected with APP-specific siRNA displayed no detectable staining of cytoplasmic viral particles despite an abundance of gE, which often co-localizedd with VP26-GFP particles (Figure 7B).

Cytoplasmic viral particles labeled with VP26-GFP did co-localize with APP in the nuclear area, while few viral particles were found in the peripheral cytoplasm.

Cytoplasmic aggregate particles were purified using a fluorescence‐activated cell sorter (FACS) by monitoring EGFP fluorescence, whereas nuclear aggregates were purified by using the detergent insoluble nature of aggregates.