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2550 spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The 2550 spectrophotometer is a laboratory instrument designed for precise and reliable absorbance measurements. It utilizes a single-beam optical system to analyze the light absorption properties of liquid samples across a wide range of wavelengths. The 2550 spectrophotometer features a compact and durable design to support routine laboratory applications.

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12 protocols using 2550 spectrophotometer

1

Nanoparticle Characterization and Catalytic Analysis

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The particle sizes of the prepared nanoparticles were calculated from the X-ray diffraction data (Philips PW1710 diffractometer, CuKα radiation, Holland) using the Scherrer equation. The surface morphologies, particle sizes, and various contours of the nanocatalyst powders were analyzed by transmission electron microscopy (FEI TITAN G2 80-300) operated at 300 keV. Diffuse reflectance UV-Vis spectra of the nanocatalysts were recorded using a Shimadzu 2550 spectrophotometer equipped with an integrating sphere accessory using BaSO4 as the reference material. Raman spectra were recorded using an inVia Raman spectrometer (Renishaw, UK) operating at a wavelength at 785 nm with a resolution of 1 cm−1. The magnetization measurements were performed with a physical property measurement system (Quantum Design PPMS-II) under ambient conditions. The total organic carbon (TOC) for all the samples was analyzed by direct injection of the filtered sample solution into a TOC analyzer (Shimadzu TOC-VCPH model). Prior to the TOC analysis, the instrument was calibrated with potassium hydrogen phthalate. TOC0 is the TOC measured after the equilibrium adsorption of the dye on the nanocatalyst surface, and the TOCs obtained at various irradiation times are denoted as TOCt.
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2

Characterization of Microgel Particles

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The 1H NMR spectra of the microgel was studied using a VARIAN 400 spectrometer (400 MHz). Transmission electron microscopy (TEM) images were obtained using a JEOL (Tokyo, Japan) 2100 microscope operated at 200 kV. Field emission scanning electron microscopy (FESEM) studies were performed on a JSM 7600 F microscope (JEOL, Tokyo, Japan) at 5 kV. UV-Vis spectra of the samples were recorded using a Shimadzu (Tokyo, Japan) 2550 spectrophotometer. Finally, the size of the composite particles dispersed in water (20 mg/mL) was determined by Malvern Nano ZS dynamic light scattering (DLS) varying from 20 to 50 °C.
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3

P-selectin UV Spectrum Assay

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The sample diluents for P-selectin UV spectrum were from rat ELISA kit (Rat P-selectin ELISA Kit; Wuhan Huamei Biotech Co., Ltd., Wuhan, Hubei Province, P. R. China). A solution of P-selectin in sample diluents was prepared (300 ng/mL), from which 300 μL was added into six eppendorf tubes. The control tube only contains 300 μL of sample diluents. The sample tube contains 300 μL solution of P-selectin in sample diluents (300 ng/mL) and 10 μL solution of THPDTPI in sample diluents (final concentration: 0.5, 4.8, 5.0 and 5.4 μM). All tubes were incubated at room temperature for 12 h then received UV test on a Shimadzu 2550 spectrophotometer.
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4

Characterization of Nanomaterials by Advanced Techniques

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Transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDS) were carried out by using a JEOL JEM-2100F transmission electron microscope at 200 kV. X-ray diffraction (XRD) patterns were measured by using a Rigaku D-MAX/A diffractometer at 35 kV and 35 mA. UV–vis measurements were conducted on a Shimadzu 2550 spectrophotometer. Inductively Coupled Plasma Spectrometer (ICP) analyses were performed by using a Direct Reading Echelle ICP, LEEMAN.
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5

Absorbance Spectroscopy of DNA-HMCEF Interaction

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Absorbance spectra were recorded on a Shimadzu 2550 spectrophotometer with a 1.0 cm path quartz cell. Absorption titration was performed in the quartz cell by fixing 90 μM concentration of 2 mL HMCEF, into which 10 μL of CT DNA solution was added each time in 0.42–2.53 ratios of (DNA)/(HMCEF). The titration system was incubated at 37°C for 5 min for recording the absorption spectrum.
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6

Evaluating IQCA-TAVV Binding to GPIIb/IIIa

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GPIIb/IIIa and sample diluents were commercially obtained from rat ELISA kit (Cusabio Biotech Co. Ltd, Newark, USA). A stock solution of IQCA-TAVV in sample diluents (4.38 mM) was prepared. A solution of GPIIb/IIIa in sample diluents was prepared (5.4 ng/mL), from which 300 μL was added into six eppendorf tubes. The control tube only contains 300 μL of diluents. The sample tube contains 300 μL solution of GPIIb/IIIa in sample diluents (5.4 ng/mL) and 10 μL solution of IQCA-TAVV in sample diluents (final concentration: 200 nM, 400 nM, 600 nM, 800 nM, 1.0 μM, 1.2 μM, 1.4 μM and 1.6 μM,). All tubes were incubated at room temperature for 12 h and then received UV test on a Shimadzu 2550 spectrophotometer.
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7

Quantification of P-Selectin Inhibition

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P-Selectin and sample diluents were commercially obtained from rat ELISA kit (Cusabio Biotech Co. Ltd, Newark, USA). A stock solution of IQCA-TAVV in sample diluents (4.38 mM) was prepared. A solution of P-selectin in sample diluents was prepared (300 ng/mL), from which 300 μL was added into an eppendorf tube. The control tube only contains 300 μL of diluents. The sample tube contains 300 μL solution of P-selectin in sample diluents (300 ng/mL) and 10 μL solution of IQCA-TAVV in sample diluents (final concentration: 167 nM, 330 nM, 630 nM and 900 nM). All tubes were incubated at room temperature for 12 h and then received UV test on a Shimadzu 2550 spectrophotometer.
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8

P-selectin Expression Assay with DEBIC

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Sample diluents for P-selectin expression assay were from rat ELISA kit (Rat P-selectin ELISA Kit; Wuhan Huamei Biotech Co., Ltd., Wuhan, Hubei Province, People’s Republic of China). A solution of P-selectin in sample diluents was prepared (300 ng/mL). Into an eppendorf tube 300 μL of this solution was added. The control tube only contains 300 μL of sample diluents. The sample tube contains 300 μL solution of P-selectin in sample diluents (300 ng/mL) and 10 μL solution of DEBIC in sample diluents (2, 4, 6, 8 and 10 μM). All tubes were incubated at room temperature for 12 h then received UV test on a Shimadzu 2550 spectrophotometer.
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9

Comprehensive Materials Characterization Techniques

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Transmission electron microscopy (TEM), high-resolution TEM (HRTEM), and energy-dispersive X-ray spectroscopy (EDX) were carried out using a JEOL JEM-2100F transmission electron microscope at 200 kV. The samples were dissolved in water and dropped on copper grids for inspection. UV-Vis measurements were conducted on a Shimadzu 2550 spectrophotometer. Field emission scanning electron microscopy (FSEM) studies were performed on a FEI Nova 400 NanoSEM operated at 20 keV. X-ray diffraction (XRD) patterns of the samples were recorded on a D8 Advance X-ray diffractometer (Germany) using Cu Kα radiation (λ = 0.1542 nm) operated at 40 kV and 40 mA and at a scan rate of 0.05° 2θ s−1. The Raman measurements for the samples were performed by a laser confocal micro-Raman spectrometer (RenishawinVia-Renishaw, 532 nm and 514 nm excitation wavelength, the diameter of laser spot size is around 700 nm at 100x magnification, max laser power is 50 mW with the exposure time 1 s, and the applied power was set to 0.01% for all the spectra). An amount of 10 μl solution (chemicals dissolve in ethanol) was dropped on the surface of printed Ag pattern for SERS measurements, and dried before measurements. All spectra were calibrated with the silicon Raman mode at 520.7 cm−1.
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10

UV Spectroscopy Assay for DNA Intercalation

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UV spectrum assay can visualize the intercalation of PZL318 toward DNA, and this assay was performed. In brief, after recording the UV spectrum (Shimadzu 2550 spectrophotometer, 220–350 nm wavelength; Shimadzu Corporation, Kyoto, Japan) of 40.0 μM of PZL318 in phosphate buffered saline (PBS) (3 mL, pH 7.4), 30 μL of CT DNA in PBS (pH 7.4; 6.010−4 M; final concentration: 0 μM; 6.0 μM; 12.0 μM; 18.0 μM; 24.0 μM; and 30.0 μM) was added and the spectra of PZL318 plus CT DNA was recorded to monitor the effect of CT DNA on the UV spectrum of PZL318.
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