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Scanning electron microscope analysis demonstrated that the surface roughness and growth rate of the coatings increase with the decrease of the Ar/C2H2 ratio.
Scanning electron microscope analysis demonstrated that the unique design of PPy/GH-PSS morphology is not only to control micro/nanostructure of PPy wrapped GH, but also to develop the nanostructure morphology of PPy matrix.
A transmission electron microscope analysis demonstrated that S. galbus MBR-5 entered the leaves of Rhododendron sp. seedlings through stomatal openings [91].
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Multivariate analysis demonstrated similar findings.
Her analysis demonstrated the opposite effect.
The analysis demonstrates inter-individual variation in cell population maps.
Our analysis demonstrates this is possible.
Nevertheless, soft-agar plate assays and confocal microscope analysis of static biofilms clearly demonstrate that CheR1 activity is not only essential for flagella-mediated chemotaxis but that it is also involved in the formation of structured biofilms.
These products were characterized by scanning electron microscope (SEM) analysis which demonstrated that highly aligned fiber strands were formed without beads when coated onto a mandrel rotating at 1800 rpm.
For electron microscope analysis, heart tissues were fixed with 2.5% glutaraldehyde solution (Wako: 072-02262).
For microscope analysis, the slides will be examined under microscope at 400× magnification.
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