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Uv 2600 pc spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The UV-2600 PC spectrophotometer is a high-performance analytical instrument designed for precise and accurate measurement of UV-visible absorption spectra. It features a wide wavelength range, high-resolution optics, and a user-friendly software interface for data analysis. The core function of the UV-2600 PC is to provide reliable and reproducible absorbance measurements across a variety of applications.

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10 protocols using uv 2600 pc spectrophotometer

1

Spectral Analysis of Aceclofenac-Pluronic Formulations

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Spectral measurements of the aceclofenac and pluronic samples in different combinations were conducted using Shimadzu UV-2600 PC spectrophotometer with 1 cm quartz cell. Stock solution of Acl 1000 µg ml−1 was prepared by dissolving 0.1 g of pure aceclofenac in 10 ml dimethylsulphoxide (DMSO). Then it was made up to 100 ml by adding distilled water. The solutions of 5% pluronic F108, 3% L81 and mixed pluronic were prepared in 1000 µg ml−1 Acl; and their UV- spectrophotometric measurements were recorded.
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2

Analytical Characterization of Protein Samples

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Ultraviolet-Visible spectra were recorded on a UV-2600 PC spectrophotometer (Shimadzu) and U-3310 spectrophotometer (Hitachi). ESI-TOF mass spectra were recorded on a micrOTOF II (Bruker Daltonics) using positive mode ESI-TOF method for protein solutions in 5 mM ammonium acetate buffer. FAB-MS measurements were performed on a JEOL JMS-700 instrument.
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3

Characterization of CdS Nanoparticles and Hybrid Films

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UV-vis and fluorescence spectroscopy were utilized to analyze the CdS nanoparticles and the PHV/CdS hybrid films. The UV-vis spectra were obtained using a Shimadzu UV-2600PC spectrophotometer (Shimadzu Corp., Kyoto, Japan), and the measurement range was from 200 nm to 600 nm. The Fluorescence spectra were measured using an F97Pro spectrophotometer (Lengguang Tech., Shanghai, China). The excitation wavelength of the fluorescence measurements was 380 nm, the scanning speed was 3000 nm/min, the scanning interval was 1 nm, the excitation bandwidth was 10 nm, and the emission bandwidth was 10 nm. In order to analyze the morphology of the synthesized CdS particles, transmission electron microscopy (TEM) was used, and carbon foils were used as the supports for the TEM samples. TEM images of the CdS nanoparticles were taken using a Tecnai G2 20 TWIN transmission electron microscope (Hillsboro, OR, USA). The PHV/CdS hybrid films were analyzed using a scanning electron microscope (SEM), and ITO glasses were used as the template. SEM was used to measure the morphology of the CdS and PHV/CdS hybrid films, and images were acquired using a Quanta 200FEG SEM spectrometer at 20 kV, 10 mA, SE mode, and spot size of 3.5 (Hillsboro, OR, USA).
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4

Total Sugar Quantification via Phenol-Sulfate

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Total sugar was quantified using the phenol-sulfate method (DuBois et al., 1956 (link)). A 100 μL aliquot of 5% (w/w) phenol was added to 100 μL of a sample in a glass tube and vortexed three times for 10 s. Then, 500 μL of concentrated sulfuric acid was added, and the tube was immediately vortexed three times for 10 s and then kept at 30°C for 30 min in a water bath. Sugar content was measured by absorption at 487 nm using a UV-2600PC spectrophotometer (Shimadzu, Japan, Tokyo). Any contamination of the BG11 medium was evident by slight background coloration. This background was subtracted on the basis of the extrapolation of absorption at 430 nm, where the coloration due to sugars was minimal. Glucose was used as the standard. Some EPS samples were highly viscous, so we vortexed and sonicated them before measurement. Statistical significance was determined using Welch’s t test.
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5

Characterization of Organic Compounds

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All chemical reagents were obtained commercially and used without further purification. 1H NMR and 13C NMR spectra were recorded on a Bruker AV-400 spectrometer using TMS as internal standard. Electrospray ionization (ESI) mass spectra were recorded by an LC-MS 2010A (Shimadzu) instrument. The high-resolution mass spectrum (HRMS) was measured using a Q-TOF6510 spectrograph (Agilent). The UV-vis absorption spectra were analyzed by a UV-2600 PC spectrophotometer (Shimadzu, Japan). The fluorescence spectra were recorded on a F-7000 Fluorescence Spectrophotometer (Hitachi, Japan).
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6

Structural Elucidation of Organic Compounds

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UV spectra were measured on a Shimadzu UV-2600 PC spectrophotometer (Shimadzu, Kyoto, Japan). Optical rotations were recorded on a PerkinElmer MPC 500 (Waltham, MA, USA) polarimeter. For ECD spectra, Chirascan circular dichroism spectrometer (Applied Photophysics, Leatherhead Surrey, UK) was used. NMR spectra were acquired by a Bruker Avance spectrometer (Bruker, Billerica, MA, USA) at 700 MHz for 1H and 175 MHz for 13C. HRESIMS spectra were recorded on a Bruker miXis TOF-QII mass spectrometer (Bruker, Billerica, MA, USA). X-ray diffraction intensity data were measured on an Agilent Xcalibur Nova single-crystal diffractometer (Santa Clara, CA, USA) using Cu Kα radiation. TLC and column chromatography were performed on plates precoated with silica gel GF254 (10–40 μm) and over silica gel (200–300 mesh) (Qingdao Marine Chemical Factory, Qingdao, China), respectively. Spots were detected on TLC (Qingdao Marine Chemical Factory, Qingdao, China) under 254 nm UV light. Semi-preparative HPLC was performed using an ODS column (YMC-pack ODS-A, YMC Co., Ltd., Kyoto, Japan, 10 mm × 250 mm, 5 μm).
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7

UV-Vis and ESI-TOF Spectroscopy Protocol

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UV-vis spectra were recorded on a UV-2600 PC spectrophotometer (Shimadzu). ESI-TOF mass spectra were recorded on a micrOTOFII (Bruker Daltonics) using positive mode ESI-TOF method for protein solutions.
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8

Comprehensive Characterization of Nanomaterials

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All PL spectra measurements were performed using a Hitachi F-7000 PL spectrophotometer (Hitachi Co., Ltd.) under an excitation and emission slit of 2.5 and 5.0 nm, respectively. UV–vis absorption spectra experiments were carried out using a Shimadzu UV-2600 PC spectrophotometer. High-resolution transmission electron microscopy (HRTEM) images were collected using a Tecnai F20 microscope (Philips-FEI Co., Holland) operated at 200 KV. The X-ray photoelectron spectra (XPS) were acquired using an ESCALAB 250Xi (Thermo Fisher Scientific, United States), where the analysis chamber was 1.5 × 10–9 mbar and the X-ray spot was 500 μm. The time-resolved fluorescence decay curves were obtained using an Edinburgh FLS920 PL spectrometer (Edinburgh, United Kingdom) with a 370-nm nano-LED as the excitation source. The electron spin resonance (ESR) spectra were obtained using a Bruker ESR 300 E with a microwave bridge (receiver gain, 1 × 105; modulation amplitude, 2 Gauss; microwave power, 10 mW; modulation frequency, 100 KHz).
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9

Characterization of Photocatalytic Materials

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UV-vis spectra were measured with a Shimadzu UV-2600PC spectrophotometer (Shimadzu Corp., Kyoto, Japan). Fluorescence measurements were carried out with a Hitachi (model F-4600) spectrophotometer (Hitachi High-Tech Corp., Tokyo, Japan) at room temperature. TEM images were obtained on a JEM 2100 (JEOL Co. Ltd., Tokyo, Japan) operating at 200 kV. X-ray diffraction (XRD) pattern was obtained by using Bruker D8 Focus (Bruker Corp., Billerica, MA, USA) under Cu-Kα radiation. X-ray photoelectron spectroscopy (XPS) measurements were taken on an ESCALAB 250 spectrophotometer (ThermoFisher Scientific Corp., Waltham, MA, USA) with Al-Kα radiation. The binding energy scale was calibrated using the C 1s peak at 284.60 eV. All pH measurements were made with a Model pHS-3C meter (Mettler Toledo FE20, Mettler Toledo (Shanghai) Co. Ltd., Shanghai, China). The generated amount of H2 was characterized by GC analysis (GC-2014 Shimadzu, Shimadzu Corp., Kyoto, Japan) using N2 as the carrier gas with a molecular sieve column (5 Å; 30 m × 0.53 mm) and a thermal conductivity detector.
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10

Lipid Oxidation Measurement in Meat Chops

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Following the 5-d retail display, chops were utilized for lipid oxidation measurement. Thiobarbituric acid reactive substance values were determined according to the procedure of Witte et al. (1970) (link). From each chop, a 5-g sample that contained both the interior and surface was blended with 25 mL trichloroacetic acid solution (20%) and 20 mL distilled water. Samples were homogenized using a Sorvall Omni mixer (Newton, CT) for 1 min and filtered through a Whatman (#1) filter paper. One milliliter of filtrate was mixed with 1 milliliter thiobarbituric acid solution (20 mM) and incubated in a boiling water bath (95°C) for 10 min. After incubation, samples were cooled, and absorbance at 532 nm was measured using a Shimadzu UV-2600 PC spectrophotometer (Shimadzu, Columbia, MD). The blank consisted of 2 mL trichloroacetic acid/distilled water (1:1 v/v) and 2 mL thiobarbituric acid solution.
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