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Cs2100m

Manufactured by Thorlabs
Sourced in United States

The CS2100M is a compact, high-performance single-channel power meter designed for accurate power measurements of optical signals. It features a high-speed analog-to-digital converter, providing fast response times and precise power readings. The CS2100M is a versatile and reliable tool for a wide range of photonics applications.

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4 protocols using cs2100m

1

Portable NIR-I/II Imaging System

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Based on the first-generation visible NIR-I/NIR-II integrated imaging system, an NIR-II imaging system was developed for better clinical application.16 (link) As shown in Figure 1, it has the merits of portability, light weight (4 kg), and ease of operation. An InGaAs camera (640×512 pixels, TE4-25; Hengxin, Shenyang, China) cooled to −80°C was utilized to capture images in the NIR-II window. According to the experimental requirements, NIR-II fluorescence signals were able to be extracted by various long-pass filters. For example, were a 1,100 nm image needed, we would fit a 1,100 nm long-pass filter (ThorLabs, Newtown, NJ, USA) to the camera, limiting wavelength <1,100 nm to pass through the lens. A silicon camera (1,920×1,080 pixels, CS2100M; ThorLabs, Newtown, NJ, USA) equipped with a 900 nm short-pass filter was used to acquire images in the NIR-I window. In both NIR-I window and NIR-II window fluorescence imaging, a 785 nm laser (Ningbo Yuanming Laser Technology, Zhejiang, China) beam was exploited to provide uniform illumination extended through a lens on the region of interest (ROI), and the excitation wavelength was filtered away by 800 nm long-pass filters. The facular power density was consistently adjusted to 10–15 mW/cm2 during testing.

NIR-I/II fluorescence imaging system used for in vivo NIR fluorescence imaging in porcine limbs.

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2

Intrinsic Optical Imaging of Olfactory Bulb

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Intrinsic optical imaging of the olfactory bulb18 (link) was done using a pair of back-to-back SLR lenses with a 50 mm f/1.4 lens used as objective and a second lens Tamron AF 90 mm f/2.8 Di SP AF/MF 1:1 Macro Lens coupled to an sCMOS camera (CS2100M, Thorlabs). The camera was fitted with a long pass filter with a cut-on wavelength of 500 nm (FELH0500, Thorlabs). This setup resulted in a resolution of 3.3 µm per pixel. White light from a flashlight was used to find the surface of the olfactory bulb. The imaging plane was set between 200 and 250 µm below the vasculature on the surface of the bulb. Single odors and odor mixtures were presented for 9 s randomly interleaved.
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3

Hyperspectral Imaging of Retinal Cross-Section

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We built an HSI system based on an Olympus IX83 microscope. Figure S1 shows the photographs of the system parts. The samples are illuminated by a broadband halogen lamp, and the transmitted light is collected by a 10 objective lens (Olympus, 0.25 NA). The output image is filtered by a liquid crystal tunable filter (KURIOS-VB1, Thorlabs) in narrow bandwidth setting (10 nm FWHM at λ = 550 nm). The spectral range is from 420 to 720 nm, with a wavelength scanning step of 2 nm. We collected the image data using a monochrome sCMOS camera (CS2100M, Thorlabs). In total, 151 spectral images were captured for one FOV. The entire cross-section of the retina ST was scanned with a 1/3 overlap between adjacent FOVs for image stitching. A sample not in imaging was attached to a glass slide without a cover glass and kept in PBS 1× solution. When performing imaging, we placed a cover glass on top of the sample and replenished it with PBS 1× solution to keep the tissue moist. All retinal cross-section samples were kept in PBS 1× solution over 2 weeks and reimaged multiple times. Upon completion of scanning, we stitched all the FOVs at the selected wavelength to a whole strip view of the retina cross-section.
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4

Quantifying Calcium Dynamics in Human Engineered Cardiac Tissues

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Tyrode solution was prepared with the following composition: NaCl 134 mM, KCl 2.68 mM, MgCl2 1.05 mM, CaCl2 1.80 mM, NaH2PO2 400 μM, NaHCO3 12 mM, Glucose 5.56 mM. The pH was adjusted with NaOH to reach 6.5. The chemicals were purchased from Fisher Chemical and Sigma-Aldrich. All solutions were prepared using deionized water (~18 MΩ) either from a water purification system (Ultra Purelab system, ELGA/Siemens) or purchased from Thermo Scientific (AA36645K7). Spontaneous Ca2+ release activity of the hECTs was monitored with Ca2+ sensitive fluorescent dye Fluo-4 (10 mM Fluo-4 AM) diluted in Tyrode solution for 45 min near 32 °C. A scientific CMOS camera recorded spontaneous Ca2+ transients at 15 frames per second (Thorlabs, CS2100M). Custom Matlab script was used to analyze the video’s temporal changes of the fluorescence intensity at different ROIs. The intensity of each frame was normalized to a background baseline recorded without the sample. Ca2+ dynamics were quantified by computing time to peak intensity, time to 90% decay of Ca2+ signal intensity, and full width at halfmaximum of the Ca2+ transient. The calcium transients were recorded from at least three different ROIs per biological replicate and two biological replicates were used for each condition. For the quantitative analysis of the calcium dynamics, a total of 50 transients were used per condition.
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