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Immunoelectron microscopy of granule cells provided evidence that Unc51.1 indeed associates with membrane vesicles.
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In addition, we reported confocal microscopy of lytic granules on actin filaments detected by STED.
Scanning electron microscopy of isolated PHB granules of Synechocystis sp. PCC 6714 cultivated under nitrogen and phosphorus limitations showed an average diameter of 0.7 µm.
The organization of the semi-crystalline shells has been widely studied by scanning electron microscopy of thin sections of granules [ 16, 17], nevertheless, detailed knowledge regarding the structure, organization and arrangement of lamellae is still limited.
Brightfield microscopy showed a wide range of granule sizes in wild-type starch, and neither knockdown of GBSS nor overexpression of SBEII had any obvious effect on the size range distribution of the granules.
Transmission electron microscopy of enzyme-isolated, spray-dried granules revealed a retention of the surface shell throughout the reaction with conversion of the core to a porous lamellar texture.
As depicted in Figures 10 and 11, electron microscopy revealed three types of granules in the mast cells of the colonic mucosa, intact, PMD and AND.
Remarkably, the estimate of granule size from the NMR diffusion measurements is in excellent agreement with the overall particle size that was measured by SEM and optical microscopy.
Time-lapse microscopy of P bodies (DCP1a-GFP) and stress granules (G3BP2-GFP) in arsenate-stressed HeLa cells.
Scanning electron microscopy of the almond nuts showed that the starch granules were embedded in tissues.
Electron microscopy of the pancreatic β cells also revealed that cell size, total number of granules per section and mean granule diameter were similar in WT and KO β cells (Fig. 2C F).
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