Sentence examples for microscopy at low from inspiring English sources
Especially, the TAFII5 N-terminal domain is required for its incorporation within TFIID and immuno-labelling experiments carried out by electron microscopy at low resolution have suggested that this domain might homodimerize, possibly explaining the three-lobed architecture of TFIID.
Field enhancement of the In2O3-coated SWCNTs is confirmed by conductive atomic force microscopy at low electric field (contact mode: 1 V to −1 V) and also field emission (FE) analysis at high electric field (0 4.2 V/μm).
The membrane was mounted and invaded cells were visualized using fluorescence microscopy at low magnification.
From each specimen, two sections were initially examined under light microscopy at low magnification (×100).
Most of these infections were helminths, of which the eggs could be easily found with microscopy at low magnification of an unstained wet mount of the concentrated sample.
To determine the MVD, sections were scanned under light microscopy at low power (× 100), and three most vascular areas (vascular hot spots) were chosen.
The immunostained sections were scanned by light-microscopy at low magnification (40×) and the areas of tissue with the greatest number of distinctly highlighted microvessels ('hot spots') were selected.
Our findings highlight that for transmission electron microscopy performed at low energies (energies <100 keV) thick hybrid pixel detectors provide an advantageous architecture for direct electron imaging.
Sphere micelles were observed by transmission electron microscopy (TEM) at low copolymer concentration (6 × 10−5 g/mL), but the micelle shape became irregular when the copolymer concentration increased to 6 × 10−4 g/mL.
Micrograph comparison of particle-free agarose and PVA slices, observed by scanning electron microscopy (SEM) at low magnification (Figure 1), has shown that both types of the cryogel monoliths had quite similar structures with evenly distributed interconnected pores, with an average pore size within the range 4 to 100 μm.
PD assessment is facilitated in malaria because serial parasite densities are readily assessed by microscopy, and at low densities by quantitative PCR, so that initial therapeutic responses can be quantitated accurately.
