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Cary 60 uv vis spectrometer

Manufactured by Agilent Technologies
Sourced in United States, Germany

The Cary 60 UV-Vis spectrometer is a compact, high-performance instrument designed for accurate and reliable UV-Vis spectroscopy. It measures the absorption or transmission of light in the ultraviolet and visible regions of the electromagnetic spectrum.

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86 protocols using cary 60 uv vis spectrometer

1

Characterizing Silver Nanoparticles via UV-Vis

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The easiest method to confirm the formation of NPs remains UV-Vis spectroscopy. A Cary 60 UV-Vis spectrometer (Agilent, Santa Clara, CA, USA) was employed. Distilled water (dH2O) was used as a reference, and the absorbance spectrum of the AgNP sample was measured in the 200–800 nm region [17 (link)].
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2

Quantifying Encapsulated Catalase Protein

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To measure the total
protein content, the optimized procedure for CAT released from SLMs
described in the section “Evaluation of
CAT Activity after Encapsulation
” was employed. After
complete solubilization of the SLMs and addition of the 10 mL of phosphate
buffer (50 mM, pH 7), the aqueous phase was assayed spectrophotometrically
(Cary 60 UV–vis spectrometer, Agilent Technologies GmbH, Waldbronn,
Germany) at 280 nm.23 (link) Each formulation
was analyzed in triplicate and the results were expressed as mean
± standard deviation (S.D.).
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3

Characterization of Organic Compounds

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All chemicals were from commercial sources and were used without further purification. NMR spectra were acquired with an Avance Neo 400 spectrometer from Bruker (Billerica, MA). UV–vis experiments were carried out with a Cary 60 UV–vis spectrometer from Agilent Technologies (Santa Clara, CA) with measurements every 0.1 s for kinetic experiments. The phrase “concentrated under reduced pressure” refers to the removal of solvents and other volatile materials using a rotary evaporator at water aspirator pressure (<20 Torr) while maintaining a water-bath temperature of 40 °C. Residual solvent was removed from samples by the vacuum (<0.1 Torr) achieved by a mechanical belt-drive oil pump. All procedures were performed in air at ambient temperature (~22 °C) and pressure (1.0 atm) unless indicated otherwise.
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4

PCS-catalyzed Propionyl-CoA Synthesis

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The competition contained 3 mM CoA, 2 mM 3-hydroxypropionate, 200 µM NADPH, 5 mM ATP, 7.5 mM Mg2Cl, 60 mM KCl, 100 mM KHCO3 and 100 mM Tris-HCl pH 7.8. For the competition either 100 µM 13C-3-hydroxypropionyl-CoA or 100 µM 13C-acrylyl-CoA was added. The assay was started with 2 µL of 1.28 mg/mL PCS wt and the reaction monitored photospectrometrically at 340 nm using a Cary-60 UV/Vis spectrometer (Agilent Technologies Inc. Santa Clara, CA, USA) at 30°C using quartz cuvettes (10-mm path-length; Hellma® (Germany)). The assay was quenched after a ΔAbs of 0.36 that corresponds to a turnover of 60 µM. The isotopic pattern of the produced propionyl-CoA was analyzed by hrLC-MS.
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5

Comprehensive Characterization of Graphene Quantum Dots

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Sample morphologies were examined with a Phillips CM300 transmission electron microscope (TEM) operated at 300 kV. Atomic force microscopy (AFM) topographic measurements were performed with a Molecular Imaging PicoLE SPM instrument. UV-vis absorption spectra were acquired with an Agilent Cary 60 UV-vis spectrometer using a 1 cm quartz cuvette, and steady-state photoluminescence measurements were performed with a PTI fluorospectrometer. FTIR measurements were performed on a PerkinElmer FTIR spectrometer with samples deposited onto a ZnSe disk. Raman spectra were acquired with a DeltaNu Advantage 532 Raman system powered by a 532 nm laser. XPS measurements were carried out with a PHI 5400/XPS instrument equipped with an Al Kα source operated at 350 W and 10−9 torr. 1H and 1H–13C HSQC (heteronuclear single quantum coherence) NMR measurements were carried out with a Varian Unity 500 MHz NMR spectrometer using saturated GOQD or rGOQD solutions in D2O.
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6

UV Spectroscopy of Protein Redox State

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UV spectra were collected on a Cary 60 UV–vis spectrometer (Agilent) with Cary WinUV 5.1 software. Measurements were performed over a spectral range of 200–800 nm at a scan speed of 300 nm/min with 0.5 nm data intervals. The buffer solution baseline was automatically subtracted.
After collection of the first spectrum, mDna2 at 25 μM was incubated at 4 °C for 20 h, in a similar setup to the one used in EMSAs. After the collection of the spectrum after 20 h, TCEP was added to a final concentration of 57 mM and incubated for 30 min.
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7

In Vitro Dissolution of Solid Dispersions

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The USP paddle apparatus (Pharmatest, Steinheim, Germany) was used with a rotating speed of 50 rpm. For CBZ and TBM, samples of pure drug, physical mixes, or loaded MPs (size fraction 150–250 μm) were added to 500 mL of the respective dissolution medium maintained at a temperature of 37 °C. The aqueous solution was filtered and continuously pumped (12.5 mL/min) to a flow cell in a Cary 60 UV–Vis spectrometer (Agilent Technologies GmbH, Waldbronn, Germany) and absorbance values were recorded at 285 nm and 231 nm for CBZ and TMB, respectively. In case of CIN, samples of pure drug and loaded MPs (size fraction 150–250 μm) were added to 1 L of phosphate buffer solution pH 6.8 at 37 °C. At specific time points, 2 mL of the medium were withdrawn using an 8 µm filter to avoid the removal of the MPs and the amount of drug was quantified by HPLC. Two mL of fresh medium were added to keep the volume constant. The amount of solid dispersion (and physical mixtures) was 80-100 mg for samples containing CBZ and TBM, whereas 10–15 mg for samples containing CIN. The dissolution tests were performed on six samples.
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8

Photostability Characterization of Fluorescent Dyes

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Cary 60 UV-Vis spectrometer from Agilent technologies was used to measure absorbance. Fluorescence was measured using the Cary Eclipse (Varian, USA), Horiba Fluorelog 3 (Horiba, Japan).
Photostability measurements were performed using Xenon lamp and Horiba Fluorolog 3 (Horiba, Japan). Dye and particles were excited using white light excitation, slit width of 14.7nm. Fluorescence was recorded every 30 seconds. Every point in figure 1D is the average of 10 data points taken every 0.1s using a slit width of 3 nm. For the rest of the study, fluorescence was measured using slit width 1 nm.
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9

Nanoparticle Characterization by Spectroscopy

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UV–Vis spectroscopy was performed using a Cary 60 UV–Vis spectrometer (Agilent Technologies, Santa Clara, CA, USA). Transmission electron microscopy (TEM) and energy-dispersive X-ray (EDX) mapping were performed using an FEI Tecnai F20 transmission electron microscope (FEI Company, Eindhoven, the Netherlands). The hydrodynamic size of the nanoparticles was measured using ζ-potentials (ELS-Z, Otsuka, Japan). Fourier transform infrared (FT-IR) spectra were recorded on a PerkinElmer spectrometer in the range between 4000 and 400 cm−1.
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10

Recombinant Protein Expression in E. coli

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E. coli BL21(DE3)pLysS was used to express recombinant protein from Invitrogen; glycerol and NaCl came from Scharlau; Chicken egg white lysozyme was from Fluka; ANS, ampicillin, and benzonase were from Sigma and IPTG was purchased from Biobasic. NuPAGE 4–12% bis- tris-gel from Life technologies; pre-packed Ni-NTA column was from GE Healthcare Life Sciences. Cary 60 UV–Vis spectrometer and Cary Eclipse spectrofluorometer were from Agilent technologies, Innova 44R Shaking incubator was from New Brunswick, Thermomixer was from Eppendorf, and Circular dichroism spectroscopy (CD) was from Jasco.
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