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Labview 6

Manufactured by National Instruments
Sourced in United States

LabView 6.1 is a graphical programming environment for test, measurement, and control systems. It provides a platform for designing and executing virtual instruments, which are software programs that emulate the functionality of physical instruments.

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39 protocols using labview 6

1

Confocal Imaging and Mechanical Loading of Bone

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Confocal time-lapse images were synchronized with a rest-inserted mechanical loading protocol to eliminate out-of-focus motion artifacts resulting from deformation of the bone sample, with images being acquired every 5 seconds for 900 seconds total [28 ]. Five baseline images were acquired before mechanical loading was initiated via a trigger from the FluoView software to a 16-bit data acquisition (DAQ) card (NI USB-6210) and LabVIEW VI (National Instruments, Austin, TX, USA). Samples were maintained in supplemented cell culture media while cyclic mechanical loads were applied along the long axis of the whole bone using a custom-designed system [28 ]. A pre-load of 2 N was maintained, followed by cyclic axial loading of 1 Hz triangle waveforms with 4 s rest-insertion after each cycle to allow for confocal image acquisition. Two loading conditions were applied to samples from each treatment group: 24 tibiae (8 per treatment group) were mechanically stimulated at a load magnitude of 10 N, while another 24 were stimulated at load magnitudes to match an anteromedial cortical bone strain of 2000 με between treatment groups as determined by strain gauging experiments (see later strain measurement section).
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2

Phosphorus Removal in SBR System

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The EBPR system was a sequenced batch reactor (SBR) with 8 L volume, operated at hydraulic retention time (HRT) of 18 h and SRTs of 8, 3.5 and 3 days (operational conditions are summarized in Table 1). The initial operation sequence was 2 hours of anaerobic phase, 3 hours of aerobic phase and 1 hour of settling and idle phase. The reactor was fed during the first 2 minutes of the anaerobic phase. The SBR was fed with pre-clarified wastewater from Lundtofte WWTP (Kgs. Lyngby, DK) and spiked with synthetic wastewater supplemented with propionate and ortho-phosphate. 200 mg-COD/ml of propionate were dosed to avoid organic carbon limitation, simulating propionate dosing strategies based on primary sludge fermentation (Chanona et al., 2006) . It should be noted that Lundtofte WWTP relies on chemical precipitation for phosphorus III -6 removal due to the low influent content on organic carbon. Phosphate was dosed to ensure that incoming phosphorus levels ranged between 6-10 mg-P/L. Oxygen was supplied from a pressurized air-line and was manually controlled via needle valve manipulation. The system was inoculated with biomass from a full-scale wastewater treatment plant (Lynetten WWTP, Copenhagen, DK). The SBR operation was controlled using LabView VI (National Instruments, Austin, USA).
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3

Lateral Movement on Oversized Treadmill

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All walking occurred on an oversized treadmill—belt width 1.39 m (Tuff Tread, Willis, TX)–providing space to comfortably side-step left or right (Fig 1a). Subjects wore a trunk harness attached to a passive overhead safety support (Aretech, Ashburn, VA). The safety system provided no bodyweight support and was adjusted to allow unrestricted travel across the treadmill.
A 60-inch monitor mounted 1.8 m in front of the treadmill provided real-time visual feedback of subjects’ lateral position. A single black visual feedback marker displayed on the monitor was calculated as the midpoint of a line drawn directly between reflective markers placed over each greater trochanter (Fig 1a).
39 reflective markers were placed on the pelvis and bilaterally on the lower limbs using a 6-DOF cluster marker setup. A 10-camera motion capture system (Qualysis, Gothenburg Sweden) recorded the 3D marker coordinates at 100 Hz and streamed data in real-time to a custom LabVIEW VI (National Instruments, Austin, TX) that created the visual display. As subjects moved left or right, the visual feedback marker moved simultaneously using 1:1 scaling. Only lateral position information was displayed to limit the cognitive demand on the subjects.
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4

Wearable Foot Pressure Monitoring System

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The Laboratory Virtual Instrument Engineering Workbench (LabVIEW VI, manufacturer National Instruments, Austin, TX, USA) is used as a system-design platform and development environment to display the collected data in a numerical and graphical representation (Figure 2d). The application of LabVIEW VI software v.2015 is primarily dedicated to monitoring the real-time signals from sensors via Bluetooth communication. Figure 2a shows testing socks and three SF sensors with CNF piezoelectric material. Testing socks are coupled with an electronic controller (ESP 32, manufacturer Espressif Systems, Shanghai, China) that is the low-power system on a chip microcontroller (Figure 2b,c) used to sense the foot pressure through the analog to digital conversion (ADC) port. The sensors were stitched on socks in 3 locations shown in Figure 2a (the toe, midsection and heel), using stainless steel conductive thread. The conductive thread helps to transfer the current and does not affect the human skin. Figure 2c,d shows that the microcontroller was covered up with the 3D-printed case for safety purposes. The volunteer testing with the developed sensors and sensing data collection through Lab view software is presented in Figure 2e [Video S1: movement analyses].
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5

Raman Spectroscopy of Thin Films

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Raman signals were obtained using a Horiba Jobin-Yvon HR800 UV Raman spectrometer fitted with a Horiba Jobin-Yvon Synapse CCD. The system used a Quantum Laser Torus 532 nm laser with an air corrected Leica 50×/0.55NA objective and 1 mm spectrometer entrance pinhole. When measurements were made through a 1 mm thick quartz substrate, this resulted in an effective size of the detection area of around 14 μm diameter (determined by mapping features of known sizes) and approximately 5 mW intensity at the sample. A 600 g per inch grating was used and centred around 1300 cm -1 . Labspec 5 software was used in all cases to set up the Raman spectrometer. However, Raman signals were directly readout from the CCD using a custom Labview VI (National Instruments Corp., UK) programme that was developed to synchronise the operation of the CCD and the pressure control system (MFCS-1000, Fluigent, Villejuif, France).
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6

Osteocyte Mechanotransduction under Cyclic Loading

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Samples were maintained in supplemented cell culture media while cyclic mechanical loads were applied along the long axis of the whole bone using a custom-designed system (22 (link)). A pre-load of 2 N was maintained to stabilize the bone sample, followed by 175 loading cycles of 1 Hz triangle waveforms with 4 s rest-insertion after each cycle to allow for confocal image acquisition. Load magnitudes of 10.2 N and 8.3 N were applied to the 5-month-old and 22-month-old tibiae respectively, corresponding to a surface strain of 1500 μƐ on the anteromedial cortical bone surface (25 (link)) where the osteocytes are being imaged. Confocal time-lapse images were synchronized with the rest-inserted mechanical loading protocol to eliminate out-of-focus motion artifacts resulting from deformation of the bone sample, with images being acquired every 5 seconds for 900 seconds total (22 (link)). After the acquisition of static five baseline images, mechanical loading was initiated via a trigger from the FluoView software to a 16-bit data acquisition (DAQ) card (NI USB-6210) and LabView VI (National Instruments, Austin, TX, USA) and subsequent images were acquired immediately following the completion of a load cycle.
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7

Leg Strength Assessment Protocol

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The assessment of maximal voluntary and explosive strength was carried out on both legs separately in the leg-press position using a customized apparatus featuring a force plate. The knee angle was fixed at an angle of 100°. Signals were amplified by a DMCplus device (HBM, Darmstadt, Germany) and recorded with LabVIEW 6.1 software (National Instruments, Austin, USA). Maximum voluntary strength (Fmax) was determined as the maximum value of force distribution and explosive strength (Fexpl) as maximum force increase.
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8

Exposure System for GSM-Modulated RF-EMF

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The exposure system was kindly loaned to us by Prof. Laura Calzà (University of Bologna). The exposure system and the dosimetry were previously described in great detail [75 (link),76 (link)]. Briefly, the system is composed of two twin “Transverse Electro Magnetic (TEM) cells” with two independent power supply chains (two GSM signal generators and two EMF amplifiers) to obtain sham and exposed samples at the same time, and it was positioned inside a Heraeus incubator (B-5060, Heraeus, Hanau, Germany) (37 °C, 5% CO2). Each TEM cell has a squared cross-section (14 cm wide) and can contain 6 4-multiwell plates (66 mm × 66 mm external size). The RF-EMF (900 MHz; GSM basic with pulsed modulation at 217 Hz) is uniformly absorbed in the two wells of the two symmetric plates closer to the inner copper septum of the TEM cell, resulting in a SAR of 1 W/Kg. Therefore, only the septum-adjacent wells were used in the experiments in accordance with Del Vecchio et al. [75 (link),76 (link)]. The system was controlled by LabVIEW 6.1 software (National Instruments, Austin, TX, USA). Experiments were conducted in blind modality. In each assay, cells were plated and allowed to adhere overnight and then exposed to 900 MHz GSM-modulated RF-EMF at SAR of 1 W/kg or to sham. After 48 h of exposure, DNA was extracted from each sample.
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9

Characterization of Functionalized Nanopores

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The unmodified and modified pores were characterized by measuring the currentvoltage (I-V) curves before and after functionalization. The electrolyte solutions were prepared in 10 mM tris-buffer. The measurement of I-V curve was performed using a picoammeter/voltage source (Keithley 6487, Keithley Instruments, Cleveland, Ohio, USA) and the LabVIEW 6.1 software (National Instruments). For this purpose, the single-pore as-prepared membrane was fixed between the two compartments of the conductivity cell. An aqueous electrolyte was filled in both halves of the cell. The electrodes consisting of a Ag wire coated with AgCl were inserted into each half-cell solution to establish a transmembrane potential difference (voltage V) and the ionic current I through the pore was then measured. In the present case, the ground was placed on the big opening side and the electrodes facing the tip side of the conical nanopore. Then a scanning triangle voltage signal was applied from 1 to +1 V across the membrane to record the I-V curves.
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10

Telemetric Core Temperature Measurement

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Telemetric measurement of core temperature was accomplished using a commercial system from Data Sciences International (Saint Paul, MN) that consists of a Data-Exchange Matrix, Physio-Tel Receiver (Model RPC-1), Dataquest ART 4.2 software, and an implantable battery-powered temperature sensor (model TA-F40) implanted in the rat’s peritoneal cavity. The antenna system used in each direct calorimeter consists of two radio ferrite coils oriented perpendicularly to each other and epoxied underneath a Plexiglas platform that holds them 2 mm above the floor of the direct calorimeter. The antennae wires exited the calorimeter through a gas-tight port and were connected to the RPC-1 receiver base. The antenna wires located in the thermal gradient are exteriorized through a sealed port in the copper shell and are connected to the RPC-1 receiver base by adding second wire wrappings to the receiver base’s two ferrite coils so that the external wire antenna can conduct its radio signal to the receiver. All other instrument control and data acquisition were performed using custom programs written in LabVIEW 6.8 (National Instruments, Austin, Texas).
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