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Scanning and transmission electron microscopes were used to characterize the intermetallic particles, and scanning Kelvin probe microscopy was utilised in monitoring the surface potential.
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The clinical sensitivity from a NPA has been reported to be low and variable when microscopy is utilised [ 4, 5, 10].
A variety of biochemical markers of PCD, including DNA fragmentation, mitochondrial dysregulation and phosphatidylserine externalisation, as well as morphological studies of Giemsa-stained thin smears and real-time microscopy were utilised to characterise the phenotype.
Transmission electron microscopy (TEM) was utilised to analyse both crack tip oxides and associated deformation mechanisms in the matrix.
Every empty space was utilised.
software was utilised.
The total residual correction mode was utilised.
A multi-element baseline design was utilised.
An exploratory research design was utilised.
Purposive sampling was utilised.
A LMWH curve was utilised.
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