Hf2li lock in amplifier
The HF2LI is a lock-in amplifier designed for high-frequency applications. It provides precise measurement of signals at user-specified frequencies, enabling accurate analysis of complex waveforms. The device offers a wide range of operational frequencies, flexible input channels, and advanced signal processing capabilities.
Lab products found in correlation
16 protocols using hf2li lock in amplifier
Multimodal AFM Imaging Techniques
Dielectrophoretic Trapping of Particles
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).
Photocurrent Spectroscopy for Measuring EQE
Quartz Crystal Sensor Functionalization
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.
Single-Molecule Ion Channel Signal Analysis
Microfabrication Workflow for Biosensing
Amplitude-Modulation SKPM in N2 Glovebox
Integrated Microfluidic Blood Separation
Separating CARS Signal from TPFE Interference
Real-Time Electrical Measurements of PNPase-Modified SiNW FET
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!