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Multimode fiber

Manufactured by Thorlabs
Sourced in United States

Multimode fiber is an optical fiber with a larger core diameter that allows the propagation of multiple electromagnetic modes. It is designed to transmit light over short to medium distances, typically used in local area networks, industrial applications, and some telecommunications systems.

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6 protocols using multimode fiber

1

Fiber-Optic Surface Plasmon Resonance Sensing

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The schematic diagram of the sensing system is shown in Fig. 6(a). The white light from the halogen source (Ocean Optics Inc., DH-2000-BAL) firstly transmits into the fiber optic SPR sensor through the transmission fiber (Thorlabs Inc., multi-mode fiber with 600 μm core) and coupler. Then the white light is modulated by external environmental solutions in the sensing region when the sensor is immersed into the target solution. Finally, the modulated light is reflected back by the Ag reflector and collected by a USB 4000 spectrometer (Ocean Optics Inc., 200–1100 nm). After a normalization process (detailed in our previous study22 (link)), the SPR spectrum is obtained. Our normalization process can dynamically detect the lowest point of the SPR dip and effectively eliminate the background noise.
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2

Optical Transmittance and Propagation Loss

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To measure the optical transmittance of the elastomer material, the elastomer was cured in a 1-cm quartz cuvette. The transmittance was measured by using an Evolution 300 spectrophotometer (Thermo Scientific, Waltham, MA, USA). To quantify propagation loss, we coupled light into the elastomer waveguide by using a multimode fiber with a numerical aperture of 0.22 (Thorlabs, Newton, NJ, USA). The fiber was coupled to a diode-pumped solid-state laser delivering light at 445 nm (Civil Laser, Hangzhou, China). The fiber was stripped of the acrylate coating, and 2 to 3 mm of the bare fiber was inserted into the center of one end of an elastomer waveguide. To measure the propagation loss of the waveguides, the cut-back method was used. The transmitted power through the waveguide was measured while the waveguide was suspended in air, or placed on top of strips of scleral tissue dissected from fresh porcine eyeballs. The transmitted power through the waveguide was measured with a double-integrating sphere (IS200-4; Thorlabs) at waveguide lengths of 60, 45, 30, and 15 mm. The experiment was repeated with at least three waveguides for each thickness (0.8, 1.0, and 1.4 mm). The data were adjusted to compensate for material absorption and fit to an exponential decay model (see theory below) to extract the scattering loss coefficients to air and scleral tissue.
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3

Optogenetic Stimulation of Cortex

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We used a laser system with two wavelengths for optogenetic stimulation (473 nm, blue laser) or control (594 nm, yellow laser). Laser light was delivered to cortex through a 100 μm or a 200 μm diameter multimode fiber (Thorlabs). Fiber endings were placed just above the cortical surface in area 21a. The intensity and waveform of the laser were controlled via a custom circuit in TDT, and timing was controlled by the visual stimulus computer using Psychtoolbox-3, a toolbox in MATLAB (MathWorks)108 (link).
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4

Optogenetic Manipulation and Validation

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The viruses (pAAV-CaMKIIα-NpHR3.0-EYFP and/or pAAV-CaMKIIα-EYFP) were obtained from Obio Technology CO., Ltd (Shanghai, China). The virus of more than 1012 TU/ml was used for CA1 injection. The procedure of AAV injection was the same as the injection of lentivirus using the coordinates: 2 mm (anterior-posterior) from bregma, 1.5 mm (medio-lateral), 1.5 mm (dorso-ventral). After the injection, two implantable fiber-optic cannulas made by ceramic ferrule (Φ1.25 mm) with multimode fiber (NA = 0.39, Φ = 200μm, L = 5 mm; Thorlabs, Inc. Newton, NJ, United States) were immediately implanted 0.3 mm above the injection sites. Then the optical fibers were fixed to the skull surface by using cyanoacrylate glue. Afterward, the ceramic ferrules were secured by dental cement. All the behavioral and electrophysiological experiments were conducted after 3 weeks recovery. All mice used in social interaction test were sacrificed to confirm the injection sites and virus trans-infection effect by checking EYFP under fluorescence microscope (600-FN, Nikon, Japan).
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5

Multimode Fiber Implantation for Optogenetics

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Multimode fibers of 200 μm core and 0.39 numerical aperture (Thorlabs) were used for behavior experiments. The fibers were glued to a ceramic ferrule and polished to enhance coupling efficiency. The optical fibers were implanted in the dorsal CA2 area (−2.0 mm AP, +/− 2.2 mm ML and 2.0 mm DV) 2 weeks after viral injection and fixed to the skull with dental cement. Fibers were coupled to an external fiber using standard FC connectors via a mating sleeve connected to a 589-nm laser (Laserglow).
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6

Retrograde Rabies Tracing in Amigo2-Cre Mice

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We delivered 50 nl of a G-deleted rabies helper virus AAV2/8 syn.DIO.TVA.2A.GFP.2A.B19G (UNC vector core) into the dorsal hippocampus of Amigo2-Cre mouse at the following coordinates AP -1.8 mm, ML +2.5 mm, DV -1.7 mm. Following 2 weeks of recovery and AAV expression, a second surgery was performed and 300 nl of rabies SAD.B19.EnvA.∆G.mCherry (SAD-B19 strain, Addgene Cat# 32636 prepared by the Salk institute vector core) was injected at the same coordinates. Mice were killed 7 d later and the brains cut horizontally for entorhinal cortex imaging or coronally for hippocampus imaging.
Optical fiber implantation. Multimode fibers of 200 μm core and 0.39 numerical aperture (Thorlabs) were used for behavior experiments. The fibers were glued to a ceramic ferrule and polished to enhance coupling efficiency. The optical fibers were implanted in the dorsal CA2 area (-2.0 mm AP, +/-2.2 mm ML and 2.0 mm DV) 2 weeks after viral injection and fixed to the skull with dental cement. Fibers were coupled to an external fiber using standard FC connectors via a mating sleeve connected to a 589-nm laser (Laserglow).
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