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16 protocols using hf2li lock in amplifier

1

Multimodal AFM Imaging Techniques

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The multimode imaging experiments, including SIM, PFM, and C-AFM, were performed in an AFM platform (XE-70) from Park Systems. Customized electronics were used for impedance imaging at frequencies above 50 MHz. The HF2LI lock-in amplifier from Zurich Instruments was configured to perform SIM at frequencies below 50 MHz. The DLPCA-200 current amplifier from FEMTO Inc. was used for the C-AFM imaging. The microfabricated shielded probes are commercially available from PrimeNano Inc. Finite element modeling was performed by using the commercial software COMSOL 4.4.
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2

Dielectrophoretic Trapping of Particles

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Measurement of the current and phase was performed in a solution of 10% PBS and 90% deionized water by applying an AC signal between 1 and 10 V amplitude to the trapping electrodes at a frequency of 100 kHz using an HF2TA current amplifier connected to a HF2LI Lock-In amplifier (Zurich Instruments).
The PDMS chip was primed with Pierce™ Protein-Free (PBS) Blocking Buffer during 1 h to prevent cells from adhering to the surfaces. The cells or beads were placed in a chromatography vial connected to the punched PDMS by a 360 μm outer diameter PEEK tubing (Idex). Pressure was applied to the vials using Fluigent Flow-EZ pressure controllers. The chip was mounted on and electrically connected to a custom PCB placed on the stage of a Leica DMI3000 B inverted microscope and observed using a uEye (IDS) camera. All the electric signals needed to control the positions of the particles are sent through a home made PCB creating the multiplication of an AC signal at 100 kHz and different DC signals whose amplitudes are controlled by the computer with an adapted C++ program through an analog output generator (Mccdaq USB-3100).
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3

Photocurrent Spectroscopy for Measuring EQE

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EQEPV was measured by photocurrent spectroscopy, excited by light from a 150 W quartz-tungsten-halogen lamp passing a LOT-QD MSH-D300 double monochromator and additional optical long-pass filters to reduce stray light. The incoming light was mechanically chopped at a frequency of 419 Hz and a small part was directed to a Hamamatsu K1718-B two-color photodiode for reference. The solar cell photocurrents were pre-amplified by a variable Zurich Instruments HF2TA current–voltage amplifier and the resulting voltages were again amplified and detected by a Zurich Instruments HF2LI lock-in amplifier.
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4

Quartz Crystal Sensor Functionalization

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AT cut 10
MHz quartz crystal sensors coated with a 50 nm layer of SiO2 (QSense QS-QSX303) were functionalized with polymer brushes following
the polymerization procedure, as described previously, with the exception
that the sensors were plasma cleaned in O2 (0.3 mbar, 50
mA) for 4 min instead of piranha cleaning. The sensors were clamped
in a 200 μL openQCM Q–1 cell connected to
an HF2LI Lock-in Amplifier (Zurich Instruments) controlled via OpenLAB
(Agilent). The cell was connected to a switch that could select a
dry N2 line or a line containing an acetone bubbler (330
mL/min). Before the measurements, the fundamental resonance frequency
and third overtone were locked under dry N2. A typical
measurement would start with 5 min of dry N2, 5 min of
acetone vapor, and this would be repeated once, finishing with 5 min
of dry N2. To rule out pressure effects, a blank sample
was also measured.
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5

Single-Molecule Ion Channel Signal Analysis

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The current data were recorded with a combination of HF2LI Lock‐in Amplifier (Zurich Instruments) and DL1211 preamplifier at a sampling rate of 28.8 or 7.2 kHz. The raw data with high bandwidth (10 kHz) were then used to reduce the signal noise of the circuit by a low‐pass Butterworth filter at a frequency of 2 kHz. The additional filtered processes were carried out by MATLAB 2016b. QuB or a step finding algorithm was then used to idealize the filtered data based on the hidden Markov model.[37, 39] The dwell time of each signal event and the number of total events were extracted after the idealization. The extracted data were then analyzed with Origin 9.0. The dwell time was then fitted to a single‐exponential decay function and the average dwell time was generated. Data are presented as mean ± SD. For statistical test, One‐way ANOVA testing followed by a Tukey post‐hoc test was carried out across groups. Significance was defined as p ≤ 0.05. Statistical analysis was carried out using Origin 9.0.
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6

Microfabrication Workflow for Biosensing

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Phosphate buffered saline (PBS 1X, pH = 7.2), and (3-Aminopropyl)triethoxysilane was purchased through Sigma Aldrich (St. Louis, MO, USA). SU-8 photodeveloper, SU-8 2025 photoresist, and Microposit s1813 photoresist was purchased through Kayakuam (Tokyo, JPN). Sylgard 184 elastomer base and curing agent was purchased through Dow (Midland, MI, USA). 4” borosilicate and silicon wafers were purchased through University Wafer (South Boston, MA, USA). Silver conductive epoxy was purchased through Digi-Key Electronics (Thief River Falls, MN, USA). Custom printed circuit boards (PCB) were designed and purchased through Sunstone Circuits (Mulino, OR, USA). A NE-300 syringe pump was purchased from Southpoint Surgical Supply (Coral Springs, FL, USA). A HF2LI lock-in amplifier and HF2TA current amplifier was purchased through Zurich Instruments (Zurich, SUI). MATLAB 2021b was purchased via MathWorks (Natick, USA). LabView software and a PCIe-6361 (16 bit, 2 MS/s) data acquisition card were purchased through National Instruments (Austin, USA).
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7

Amplitude-Modulation SKPM in N2 Glovebox

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The amplitude-modulation SKPM was operated combined with a Cypher S atomic force microscopy (AFM; Asylum Research, Oxford Instruments) and a HF2LI Lock-in amplifier (Zurich Instruments) in N2-filled glovebox. The resonance frequency ω0 and spring constant of AFM conducting tips are ~127 kHz and 5.0 Nm−1, respectively.
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8

Integrated Microfluidic Blood Separation

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Phosphate buffered saline (PBS, 1X and 10X), Ficoll-Paque density gradient, (3-Amino-propyl)triethoxysilane (APTES), and Roswell Park Memorial Institute medium 1640 (RPMI) were purchased through Sigma Aldrich (St. Louis, MO, USA). A NE-300 syringe pump was purchased from Southpoint Surgical Supply (Coral Springs, FL, USA). A HF2LI lock-in amplifier and HF2TA current amplifier was purchased through Zurich Instruments (Zurich, SUI). Silver conductive epoxy was purchased from Digi-Key (Thief River Falls, MN, USA). Unidentifiable human blood was obtained from Robert Wood Johnson Medical Hospital (New Brunswick, NJ, USA) through an institutional review board (IRB) study. LabView software was purchased and installed through National Instruments (Austin, TX, USA). MATLAB version 2020B was purchased and installed through Mathworks (Natick, MA, USA).
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9

Separating CARS Signal from TPFE Interference

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The TPFE signal partially overlaps spectrally with the CARS signal. The majority of the TPFE can be collected using a spectral filter but the minor overlapping part presents a substantial background to the smaller CARS signal. To separate the contribution of the TPFE from the CARS signal, homodyne detection is used, in which the Stokes beam in the CARS process is modulated (on/off). As a result, the CARS signal, which depends on the presence of the Stokes, is modulated as well whereas the TPFE that is generated predominantly by the pump beam remains constant. By detecting only the modulated part of the signal around the CARS wavelength, we separate the CARS portion. We separately verified that the Stokes beam alone does not generate any significant TPFE. The Stokes beam is modulated by an acoustic optical modulator, with a square wave at 1 MHz generated by an SFG-2110 function generator (GW Instek, Taiwan). The resulting signal from the PMT is demodulated on a HF2LI Lock-in amplifier (Zurich Instruments, Switzerland). A low-pass filter at roughly the same frequency as the pixel sampling frequency is applied, to average the demodulated signal over a single pixel.
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10

Real-Time Electrical Measurements of PNPase-Modified SiNW FET

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The PNPase-modified SiNW FET device was covered by a polydimethylsiloxane cube, which contained a hole of about 2 mm in diameter as a reaction chamber17 ,29 . The RNA substrates were kept warm at 65 °C and then quickly cooled to avoid the effect of the changeable structure. Then, a 60-μL RNA analog solution with a specific concentration was subsequently injected into the microchamber. The chamber temperature was precisely controlled with an INSTEC hot/cold chuck, which involved a proportion–integration–differentiation control system (±0.001 °C) and a liquid nitrogen cooling system. Using an HF2LI Lock-in Amplifier (Zurich Instruments), the source–drain voltage was kept at DC 0.3 V throughout all real-time electrical measurements. The current between the source electrode and the drain electrode was amplified through a DLL1211 preamplifier operating at 107 V•A−1 gain and recorded using the HF2LI Lock-in Amplifier equipped with a 5-kHz bandwidth low-pass filter at 28.8 or 7.2 kHz sampling rates.
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