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Cells were observed under the inverted microscope at indicated magnifications.
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Four areas around the femoral vein were determined at ×1 magnification under microscope as indicated in Figure 1.
Microscope analyses indicated that in vitro culturing of Kim53ΔnlpD at 28°C leads to formation of unsegmented chains containing an average of 7.2±5.6 cells/chain as opposed to the more common aggregative morphology of Kimberley53 (Figures 7B and 7A, respectively).
Microscope focusing indicated r-GV associated with and/or were within J774A.1 macrophages at 12 h post application and clearly internalized at later times (see Figures 2 and 3).
Scanning electron microscope studies indicated that lignin crosslinking is the primary reason for binding of the lodgepole pine grind at high-moisture content.
Examination of transformed cells at growing phase using an epifluorescence microscope indicated that the fluorescence localized at the most peripheral part of the cells as well as intracellular dots.
Photographs were taken after 24 h incubation at 37 °C under × 100 magnification using a light microscope indicated over 90% viability with monocytes at 2, 4, 6 and 24 h of co-culture (24 h photos shown).
Scanning Electrical Microscope (SEM) analysis indicated that rupture initiates at the notch root in the notched specimen and at the inner in the smooth specimen.
Although we did not identify the type of palatal cells at the molecular level, morphological features of the isolated cells under the microscope indicated distinct dominance of fibroblast-like cells.
After 1 h incubation, samples were washed and mounted in microscope slides as indicated above.
Several lines of evidence, including microscope observations, indicate that the gas released at high temperature is also from the fluid inclusion reservoir.
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