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Very large micron-sized ME objects with a diameter of a few microns were observed at small magnification (data not shown).
Root sections were visualized using the microscope under 20× magnification (data not shown), while the vascular bundles (stellar region) were observed at 70× magnification.
Primary muscle cell cultures were assessed for differentiation and purity by light microscopy at 4× and 10× magnification (Data not shown).
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However annexin I expression was undetectable in each of these B-cell lymphomas even at higher magnifications (data not shown).
No parasites could be seen at higher magnification (1000x, data not shown).
We analysed a large number of randomly recorded low-magnification EM data sets of HTLV-1-infected (Figure 1A) and uninfected (Figure 1B) CD4+ T cells.
For reference, the iris thickness in adult humans has been measured to be approximately 0.5 mm and from high-magnification histology data, the thickness of the ciliary body is approximately 0.2 mm [ 27, 28].
The inset represents a magnification of the data points obtained at low H2O2 concentrations.
The samples were processed to monitor FGF-2 production by immunohistochemical analysis (magnification ×20; representative data) with corresponding histomorphometric assessments as described in the Methods.
The samples were processed to evaluate the cell densities on H&E-stained histological sections (magnification ×20; representative data) with corresponding histomorphometric assessments and to monitor the DNA contents as described in the Methods.
The samples were processed to monitor matrix mineralization (alizarin red staining) and the expression of type-I and type-X collagen (immunodetection) (all at magnification ×20; representative data) with corresponding histomorphometric assessments and to estimate the type-I and -X collagen contents as described in the Methods.
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