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The mechanical properties, EDS and fracture morphology analyses were performed.
Morphology analyses were undertaken using scanning transmission electron microscopy (STEM, FEI Nova NanoSEM 200).
The size and surface morphology analyses were performed using a field emission scanning electron microscope (SEM, Hitachi SU8010, Japan).
The size and morphology analyses were performed using a field emission scanning electron microscope (SEM, Ultra55, Zeiss).
Endothelial cell morphology analyses were performed using automated measurements with the retracing method using the IMAGEnet® software program (Topcon), the manufacturer's built-in image analysis software [ 31].
Cell viability assays and DNA and chromatin morphology analyses were performed in human breast cancer cell lines to evaluate sensitivity to paclitaxel and the cell cycle response to paclitaxel.
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Chemical characterization and surface morphology analyses are performed by XRD, XPS, AFM, SEM measurements.
The primary dependent measure for the morphology analyses was the coefficient of variation (CV) to quantify the mean gap length between epidermal nerve fibers for each subject.
Full descriptions of Drosophila strains and maintenance, molecular cloning, cell culture, Western blotting, cell imaging, and retina morphology analyses are included in the Supplementary Materials and Methods.
However, the morphology-only analyses were unable to recover some of the well-established superfamilies.
Morphology and composition analyses were carried out using Raman microscopy, XPS, SEM and AFM.
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