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The core of our experimental setup reproduces a typical fluorescence microscope as illustrated in Fig. 1a.
The underlayer cracks were also observed by optical microscope, as illustrated in Figure 3d.
Penetration of the GNPs was mapped for each NP size using CytoViva HSI dark-field microscope as illustrated in Fig. 6.
Based on these enzymatic approaches, here we synthesized the giant catalytic DNA particles (~1 μm) without other inorganic core particles and successfully visualized the detection of Pb2+ utilizing a fluorescence microscope as illustrated schematically in Fig. 1.
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To measure the original contact angle, water droplets of 15 to 20 μL were placed on the zirconia surface, and a digital 300× microscope (Digimicro, Digital Microscope, Shenzhen King Leader Technology Co., Ltd., China) was used to acquire the profile images, as illustrated in Figure 2.
A probe tip from magnetic force microscope (MFM) scans over the surface of the magnetic medium whose magnetization can be reversed by the magnetic field emanated from the magnetic tip, to accomplish the recording operation, as illustrated in Fig. 6.
Slide it in as illustrated.
An alternative to achieve the magnetization reversal in the absence of the external field is to locally heat the medium using a tunneling current from scanning tunneling microscope (STM) probe to lower its crystalline anisotropy [39 43], as illustrated in Fig. 8.
The optical setup is a coherent microscope based on DH in Mach-Zehnder configuration interferometer as illustrated in Fig. 1.
Looking through the microscope, the microscopist would see a two-dimensional image and, as illustrated in Figure 4, would observe that the cell that was growing downward had grown a shorter distance than the cell that was growing horizontally.
As illustrated in the schematic in Fig. 1, the scanning laser feedback interference microscope consists of a custom-designed interferometer coupled to an inverted microscope (TE2000U, Nikon).
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