By high-resolution transmission electron microscopy, we found that the Ag NPs were fully encapsulated by PAH polymer with the complete core-shell structure.
In addition, by time-lapse microscopy, we found that the Y217F and Y217D mutants had significantly decreased ability to track microtubule plus ends (Fig. 1F and 1G).
Through scanning electron microscopy, we found the dimensional difference of uniformly distributed microridges on the inner galeae walls of Apis mellifera ligustica workers and drones.
Using transmission electron microscopy, we found the retained austenite was decomposed into ε-carbide and ferrite in the steels tempered at 300 °C for 9 h.
Through scanning electron microscopy, we found that the failure mode of the composite changed from adhesive failure to partial cohesive failure after the oxygen/argon plasma treatment.
By analyzing the spatially resolved photoresponse using scanning photocurrent microscopy, we found that the potential steps are formed in the vicinity of the electrodes/MoTe2 interface due to the doping of the MoTe2 by the metal contacts.
Using light microscopy, we found that there was no significant change in the livers of mice exposed to low dose (i.p. for 14 days, 5 mg/kg) nano-TiO2 (Fig. 4a, b).
By immunofluorescence and electron microscopy we found higher densities of mitochondria in queen larval fat body, a finding further confirmed by a citrate synthase assay quantifying mitochondrial functional units.
Using confocal microscopy, we found that long-chain (C16) fluorescent PIP2 analogs used as tracers (0.1% of total lipids) show a uniform distribution in the membrane whereas PIP2 antibodies show PIP2 clustering.
Through transmission electron microscopy, we found that the C60 incorporation efficiency reached its maximum at diameters of 1 2 nm, while the efficiency of C60 release from SWCNTs in toluene was maximized at 3 5 nm.
By confocal microscopy, we found that parasitized AA RBCs had a relatively homogeneous distribution of PfEMP-1 (Fig. 3a).
