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Differently from the pre-implant PE, where a clear polymer-associated envelope was observed, in the post implant material this signature was lost due to extensive oxidation.
The Al 2s contribution to the Al 2s/Cu 3s peak envelope was observed at ca. 119.5 eV.
Non-uniform spacing between the E. coli cytoplasmic contents and cell envelope was observed in water-treated, broth-treated, and BY07-L and CB07-L-treated cells.
Moreover, hPRR which is expressed in the envelope was observed at 5 days p.i., but not 4 days p.i. Electron micrographs revealed that purified rBmNPV-hPRR from hemolymph at 5 days p.i. possessed thick envelopes, resulting in low purification efficiency of rBmNPV-hPRR from hemolymph at 5 days p.i.
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Bulging of cytoplasm and an enlarged zona pellucida envelope were observed in a few oocytes treated with the first wash.
Compared with normal bacterial controls (Fig. 5A C), numerous bleb-like structures, membrane ruffling, cytoplasmic retraction, intracellular clumping and indentation of the cell envelope were observed with TEM in β-casein 197 exposed group (Fig. 5a c).
In contrast, minor imperfections in the nuclear envelope were observed in only 2% of nuclei from wild type imaginal discs.
The liver parenchyma and liver envelope were observed by a high-resolution transducer.
In some cells, interconnections of inner acrosomal membrane and nuclear envelope were observed and 5(b)).
The HeN1 isolate was examined by electron microscopy, and spherical viral particles with or without viral envelope were observed.
Additionally, small (diameter of ~ 10 nm) electron-dense, deposited or cellular-based granules bound to the cell envelope were observed.
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