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Using the continuous scan function, the field of view, magnified to 20 times its true size, was moved until a suitable particle was located, and then the magnification was increased by 4 or 8-fold depending on the size of the particle.
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Every other scan was analysed using Sedfit Version 9.2, (20) using the continuous size distribution (c(s)) method entering no prior knowledge.
All the samples were measured in the continuous scan mode in the 2θ range of 10 90°, using a scan rate of 0.02 deg/s.
Data was collected in the continuous scan mode from 5° to 90° 2 θ.
primarily used the continuous mode.
Use the Continuous Shooting mode.
Data were collected at room temperature from 4° to 80° 2-theta; using a continuous scan with an equivalent step size of 0.02°; and a count time of 80 s per step in theta theta geometry.
Raman spectra were performed using a Renishaw microspectrometer (Renishaw Inc. Hoffman Estates, IL) in the continuous scanning mode in the range of 40−4000 cm−1.
Conclusions: Although the above quantitative results were obtained using a specific prototype system under the experimental conditions reported in this paper, the presented evaluation methodologies can provide valuable guidelines for optimizing operational parameters in cytogenetic imaging using the high throughput continuous scanning microscopes in clinical practice.
Very large samples can be imaged using continuous scanning, with examples including paintings, ancient manuscripts, and large fossils.
Measurements are performed on a Rigaku SmartLab system (Shibuya-ku, Japan) operating with Cu Kα1,2 radiation at 30 mA and 40 kV, in the 2θ range from 15° to 100° (using continuous scan of 0.7°/s).
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