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Uv 2450 ultraviolet visible spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The UV-2450 is an ultraviolet-visible spectrophotometer manufactured by Shimadzu. It is designed to measure the absorbance or transmittance of samples in the ultraviolet and visible light wavelength ranges.

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4 protocols using uv 2450 ultraviolet visible spectrophotometer

1

Quantifying Flavonoids using AlCl3 Colorimetry

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The total flavonoid contents of the crude extract and the EtOAc fraction were determined by the aluminum chloride (AlCl3) colorimetric method with a slight modification27 (link). A volume of 0.5 mL of the sample was mixed with 0.1 mL of 10%(w/v) AlCl3 solution, 0.1 mL of 0.1 mM potassium acetate, 1.5 mL of methanol, and 2.8 mL of distilled water. After incubation of 30 min, the absorbance of the mixture was measured at 415 nm with a UV-2450 ultraviolet-visible spectrophotometer (Shimadzu Co., Kyoto, Japan). The total flavonoid content was expressed as µg quercetin equivalents per mg dry weight of the sample, and the standard curve is shown in Supplementary Fig. S5. All prepared solutions were filtered through a membrane filter (0.45 µm).
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2

Comprehensive Characterization of Nanomaterials

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TEM observations were performed with a JEOL JEM-2100 microscope operated at 200 kV (Cs 0.5 mm, point resolution 1.9 Å). High-angle annular dark-field scanning STEM was performed on a JEOL JEM-2100F microscope equipped with STEM and EDS detectors for elemental mapping analysis. TEM and STEM samples were prepared by casting a suspension of the samples on a carbon coated copper grid (300 mesh). XRD patterns were recorded on powder samples using a D/max 2500 VL/PC diffractometer (Japan) equipped with graphite-monochromatized Cu Kα radiation. XPS was performed on a scanning X-ray microprobe (Thermo ESCALAB 250Xi) that uses Al Kα radiation. The binding energy of the C 1s peak (284.8 eV) was employed as a standard to calibrate the binding energies of other elements. UV-vis absorption spectroscopy was performed on a Shimadzu UV-2450 ultraviolet-visible spectrophotometer. FT-IR spectroscopy was performed on a Bruker Hyperion 2000. 1H NMR spectra were recorded on an Avance III HD 400 spectrometer (400 MHz), and the chemical shifts were reported in ppm relative to the residual deuterated solvent and the internal standard tetramethylsilane.
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3

Comprehensive Analytical Equipment for Scientific Research

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Equipment included an electronic balance (AY120 Beijing Sedoris Instruments Co., Ltd.); SHB-IIIG vacuum pump (Zhengzhou Great Wall Technology Industry and Trade Co., Ltd.); UV-2450 ultraviolet-visible spectrophotometer (SHIMADZU Company of Japan); AC5200DTD ultrasound cleaning machine (Nanjing Anxiu Instrument Equipment Co., Ltd.); TDZ5-WS centrifuge (Changsha Xiangzhi Centrifuge Instrument Co., Ltd.); HH-2Water bath pot (Changzhou Tianrui Instrument Co., Ltd.); microplate reader (Cytation3 BioTek, Beijing China); magnetic stirrer (CL-200 Gongyi City Yuhua Instrument Co., Ltd.); freeze dryer (FDV-1200 Shanghai Ailang Instrument Co., Ltd.); and ion chromatograph (ICS-5000 Thermo Fisher Scientific Instrument Co., Ltd.).
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4

Characterization of a Complex

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1H and 13C NMR were performed with CDCl3 with a Bruker AVANCE 300 MHz. Electrospray Ionization Mass Spectrometry (ESI–MS) characterization of the complex was done by diluting complex solutions 1000 times from the original 13 mM to reach acceptable limits for use of a triple quadropole Quattro-II (Waters) instrument for low resolution analysis. For high resolution analysis a QStar Elite (AB sciex) instrument was used. Electron Paramagnetic Resonance (EPR) analysis was carried out on a Bruker instrument at 110 K, with a microwave frequency of 9.39 GHz and a modulation amplitude of 10 G. Ultraviolet–visible spectra of samples were obtained with a Shimadzu UV-2450 ultraviolet–visible spectrophotometer. Samples were exposed to air before UV–Vis spectrometer measurements.
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