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Lambda ez210 uv vis spectrophotometer

Manufactured by PerkinElmer
Sourced in United States

The Lambda EZ210 UV-vis spectrophotometer is a laboratory instrument designed to measure the absorbance or transmission of light in the ultraviolet and visible regions of the electromagnetic spectrum. It is capable of analyzing a wide range of samples, including liquids, solutions, and solids.

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3 protocols using lambda ez210 uv vis spectrophotometer

1

Serum Paraoxonase Activity Assays

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All subjects underwent blood sampling (10 ml) into heparin-containing tubes after an overnight fast. After centrifugation, the plasma was retained on ice for PON activity and TEAC assays. Reagents and ultrapure water were treated with Chelex 100 (Merck, Darmstadt, Germany) to bind transitional metals. All reagents were of pure analytical quality and were purchased from Sigma-Aldrich Chemie (Steinheim, Germany), unless otherwise indicated. All assays were carried out on duplicate samples on a Perkin-Elmer Lambda EZ 210 UV–VIS spectrophotometer (Perkin-Elmer Inc., Boston, MA, USA) or on a Cobas Mira Plus automatic analyzer (Roche Diagnostics, Basel, Switzerland). Serum PON enzymatic activity was spectrophotometrically determined using three different substrates.
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2

Characterization of Bi-Ligand Copper Nanocrystals

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UV-vis absorption spectra were performed on a Lambda EZ210 UV-vis spectrophotometer (Perkin Elmer, USA). Fluorescent spectra were performed on an F-7000 Fluorescence Spectrophotometer (Hitachi, Japan). Both of the excitation and emission slits were maintained at 5.0 nm. The morphology and mean diameter of bi-ligand Cu NCs were performed on a transmission electron microscope (TEM, JEM-2100, Hitachi, Japan). X-ray photoelectron spectra were measured on an X-ray photoelectron spectroscopy (XPS, K-Alpha, Thermo, USA). Binding energy calibration was based on C 1s at 284.6 eV. The stabilities and selectivity of bi-ligand Cu NCs were analyzed using an Infinite 200 PRO microplate reader (Tecan, Switzerland). The QY of bi-ligand Cu NCs were measured according to an established procedure. Quinine sulfate in 0.1 M H2SO4 (literature QY = 0.54) was chosen as a standard. Absolute values were calculated using the standard reference sample that has a fixed and known QY value. In order to minimize reabsorption effects, absorbencies in the 10 mm FL cuvette were kept under 0.1 at the excitation wavelength (340 nm).
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3

Characterization of Carbon Dots with Beta-Cyclodextrin

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UV-vis absorption spectra were obtained using a Lambda EZ210 UV-vis spectrophotometer (Perkin Elmer, USA). Fluorescence spectra were obtained using an F-7000 Fluorescence Spectrophotometer (Hitachi, Japan). The excitation and emission slits were both maintained at 5.0 nm and 5.0 nm. Versatile disc fluorescence/absorption spectra were recorded on Infinite 200 PRO (Tecan, USA). The morphology and mean diameter of C-dot@β-CD were obtained using a transmission electron microscope (TEM, JEM-2100, Hitachi, Japan). X-ray photoelectron spectroscopy (XPS) was conducted using an X-ray photoelectron spectroscope (K-Alpha, Thermo, USA). Cyclic voltammetry was carried out on the CHI624A electrochemical system (Chenhua Instrument, USA). Cyclic voltammograms were measured using an electrochemical workstation (Chenhua Instrument CHI624A, USA) with a conventional three-electrode system including a glassy carbon electrode as the working electrode. Ag/AgCl and platinum wire were used as the reference electrode and counter electrode, respectively.35 (link)
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