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Pci 6251

Manufactured by National Instruments
Sourced in United States

The PCI-6251 is a high-performance data acquisition (DAQ) device from National Instruments. It features 16-bit analog-to-digital conversion and can acquire data at a maximum rate of 1.25 million samples per second. The device provides multiple analog input and output channels, as well as digital input/output capabilities, making it suitable for a variety of data acquisition and control applications.

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14 protocols using pci 6251

1

Single-Molecule Fluorescence Electrochemistry

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Single-molecule fluorescence experiments were performed on a home-built Nikon Eclipse Ti-U chassis configured for total internal reflection (TIR) fluorescence using a Nikon Plan APO 100× 1.45 NA objective and a 560 nm laser source (MPB Communications). With a typical 1.4 kW/cm2 excitation illumination, the fluorescence images were filtered with an ET605/70m-2p band-pass filter (Chroma Technology Co.), and acquired on an EMCCD (iXon Ultra 897, Andor) operating at 10 frames per second. The voltage function was generated by a potentiostat (CV-27 Voltammograph) and applied on the silica-ITO working electrode with respect to an Ag/AgCl reference electrode (RE). A PCI-6251 (National Instruments) data acquisition card and a BNC-2090 breakup box were used to interface the potentiostat and the PC and to digitize the current–voltage signal.
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2

Vibrotactile Stimuli Transmission Protocol

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Vibrotactile stimuli were transmitted to participants’ hand via a mobile device mockup that they were grasping (Fig 1). The mockup was made of acrylic resin and it was similar in size to a commercial mobile phone (11 × 6 × 1 cm). A small linear vibration actuator (Tactile Labs; Haptuator TL002-14-A; 12.5 g) generated all vibrotactile stimuli that were used in both experiments. This actuator provides stronger output over a broad bandwidth (50–500 Hz, with a weak resonance at 60 Hz) than the miniature actuators that are used in commercial mobile devices. The actuator was attached to the center of the top side of the mockup using adhesive rubber tape (Fig 1, right). A computer controlled the actuator via a 16-bit data acquisition board (National Instruments; model PCI-6251) at a 20-kHz sampling rate and a custom amplifier that supplied sufficient power for the operation of the actuator. To measure the generated vibration amplitude, an accelerometer (Kistler; model 7894A500; 7.5 g) was attached at the center of the wide face of the mockup. The acceleration data were measured at 10 kHz. The total moving mass of the mockup, the actuator, and the accelerometer was 104.5 g.
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3

Electrostatic Speaker Calibration Protocol

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The speaker used in this study was an ES1 Free Field Electrostatic Speaker driven by an ED1 Electrostatic Speaker Driver manufactured by Tucker-Davis Technologies (TDT Inc, USA). The sound pressure level (SPL) of pure tones and white noise was calibrated using a 1/4" pressure prepolarized condenser microphone system (377A01 microphone +426B03 preamplifier +480E09 signal conditioner, PCB Piezotronics Inc, USA). The signals were sampled at 1 MHz by a high-speed DAQ board PCI-6251 from National Instruments and our customized Labview program was use for calibration.
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4

Calibrated Magnetic Speaker Setup for Audiological Studies

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A free-field magnetic speaker (MF1, TDT Inc., USA) was placed 1 cm away from the left ear of the animal. The speaker was driven by a stereo power amplifier (SA1, TDT Inc., USA) and calibrated using a 1/4″ pressure microphone setup with a prepolarized condenser (377A01 microphone + 426B03 preamplifier + 480E09 signal conditioner, Piezotronics Inc., USA). The captured signals were sampled at 1 MHz/s by a high-speed DAQ board (PCI-6251, National Instruments, USA). Customized LabVIEW programs were used for calibration and sound generation.
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5

Nanopore Lifetime Measurements and DNA Biosensing

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For nanopore lifetime measurements, DNA samples were diluted in 4 M LiCl, 1 x TE, pH ∼ 9.4 to make a DNA carrier of a concentration 0.4 nM by mixing the same volume of DNA carrier with 8 M LiCl pH∼ 9.4 - (2 x TE, 410 μL 2 M LiOH), then further diluting in 4 M LiCl pH∼ 9.4 - (1 x TE, 205 μL 2 M LiOH). For concentration measurements, 5 nM of biosensing DNA carrier was mixed with the target strand at the desired concentration in 1x Tris-HCl (pH 8.0) and incubated at room temperature for 3 hours before measurement. For amplifying the biotin-oligo signal, monovalent streptavidin (Howarth et al., 2006 (link)) was also added to a final concentration of 10 nM and incubated for 15 minutes at room temperature.
To measure the sample, the solution was added to the loading chamber. To connect the chip, Ag/AgCl single grounded electrode is placed in the loading chamber, and another electrode was placed in an outer chamber. To drive the DNA carrier through the nanopore, a voltage of 600 mV was applied using an Axopatch 200B amplifier (Molecular Devices), then the ionic current signal was measured. An external Bessel filter (Frequency Devices) was used to filter the signal at 50 kHz and then digitized at 1 MHz sampling rate for measurement with a data card (PCI-6251, National Instruments). LabVIEW algorithms (National Instruments) were used to collect the data and analyze it.
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6

Automated Auditory Stimulus Generation and Calibration

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A customized LabVIEW (2014 edition, National Instruments, USA) program was used for the signal waveform generation and sound calibration. The auditory stimuli were delivered via a free-field magnetic speaker (MF1, TDT Inc., USA), which was driven by a stereo power amplifier (SA1, TDT Inc., USA). A 1/4″ pressure microphone and a prepolarized condenser (377A01 microphone + 426B03 preamplifier +480E09 signal conditioner, Piezotronics Inc., USA) were used for the sound calibration. A high-speed DAQ board (1 MHz/s sampling rate, PCI-6251, National Instruments, USA) was used to record the signals. To obtain the TRF, 568 pure tones (0–70 dB SPL, 10-dB step; 0.5–64 kHz, 0.1 octave step; 35 ms duration; 5 ms sine ramp; 250 ms inter-stimulus interval) were pseudo-randomly delivered and counted as one trial.
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7

In Vivo Muscle Mechanics Imaging

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We anesthetized mice with isoflurane (1%–3%) and kept them warm on a heating pad. We shaved the hind limb, exposed the sciatic nerve and the triceps surae muscle group of the lower limb, isolated the Achilles tendon, and cut the calcaneus. We attached a force transducer (0.3 mN resolution, Aurora Scientific, 300C-LR) to the calcaneus bone piece at the tendon via a lightweight, rigid hook. We positioned the wearable microscope next to the exposed muscle and punctured the belly of the medial gastrocnemius with the microendoscope.
To initiate motor neuron activity, we stimulated contractions via the microendoscope probe while imaging the sarcomeres. The transducer reported the muscle’s contractile dynamics, which we recorded at 10 kHz and converted from analog to digital (PCI-6251, National Instruments). We determined passive muscle tension using the data from each trial prior to electrical stimulation. The force traces of Figure 4 show the total force as a function of time, minus the passive force. To determine the supra-maximal twitch force, we placed a custom-built stimulation cuff around the sciatic nerve and applied electrical stimulation (S48 Stimulator, Grass Technologies). We determined a supra-maximal stimulation level for each mouse by increasing the voltage until the twitch force amplitudes reached a plateau.
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8

Measuring Liquid Entry Pressure of Membranes

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To measure the LEP of membranes, we built a custom-designed apparatus (see Supplementary Fig. 6 and Supplementary Note 5). The tested membrane was mounted inside a filter holder, which connected to a syringe pump. By slowly pumping the salty water into the filter holder (0.1 mL min−1), the hydrostatic pressure applied on the tested membrane gradually increased. The hydrostatic pressure was monitored using a pressure sensor (IPSLU-M12, RS-Pro) and the data was recorded using a data acquisition system (PCI 6251, National Instruments). Once the applied pressure exceeded the capillary pressure of the membrane pores, liquid penetrated the membranes, leading to a pressure drop. The obtained peak value of the pressure measurement gives the LEP of the tested membrane.
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9

Ultrasonic Imaging Experimental Setup

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The measurement platform for the lensing experiment descried in the previous section is essentially a scaled-down version of the 2D scanning stage we have used for kilohertz field-mapping experiments6 (link),26 (link). As shown in Fig. 4, an ultrasonic waveguide was fabricated with laser-cut acrylic plates to confine the transmitted ultrasonic wave in a quasi-two-dimensional space. A pair of Murata ultrasound transducers (part number MA40S4S and MA40S4R) were used as the transmitter and the receiver. Two 3D printed tapered waveguiding adapters with glass tubes (about 1 mm diameter) were used to guide the ultrasonic wave from the transmitter into the waveguide, and guide the received wave from the waveguide to the receiver transducer. A LM358-based operational amplifier was used as the pre-amplification system. The pre-amplified signal was transmitted then to and be digitized by the NI PCI-6251 data-acquisition system. A two-dimensional linear stage was programmed to scan the field along the pre-defined trajectory along the focal curve.

The experimental setup of the ultrasonic imaging experiment.

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10

Microneurography and sEMG Signal Recording

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Microneurography and sEMG signals were recorded at a sampling rate of 10,000 Hz with a 16-bits data acquisition board (National Instruments PCI-6251), installed on a personal computer (PC) running a custom program written in Labview 2012 that handled the recording and the real-time processing assisting the neurologist in seeking the fibers. The pressure sensor was custom-made [24 ] and constituted by an airtight sphere-catheter system connected to a Programmable Interface Controller at its turn connected to the PC by a serial port. The recording of its data was performed at a sampling rate of 10 Hz and controlled by the aforementioned custom program. The sensor readout was shown in the GUI.
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