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Rf 6000 spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The RF-6000 spectrophotometer by Shimadzu is a high-performance instrument designed for fluorescence measurements. It features a compact design and provides accurate and reliable data collection across a wide range of wavelengths.

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7 protocols using rf 6000 spectrophotometer

1

Comprehensive Material Characterization Protocol

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TEM images and Energy-dispersive X-ray analysis were obtained with JEM-2100F. X-ray diffraction measurement was conducted on a Rigaku D/MAX-2250 V instrument (Cu Kα radiation, λ = 0.154056 nm, scanning rate of 4° min-1). Fluorescence spectra and UV-Vis spectra were recorded on a SHIMADZU RF-6000 spectrophotometer and SHIMADZU UV-2600 spectrophotometer, respectively. Elemental quantitative analysis was determined using ICP-OES. Protein quantification was determined using bicinchoninic acid protein assay. The secondary structure of protein was analyzed using chirascan CD spectrometer.
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2

Spectroscopic Characterization of Nanomaterials

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UV-Vis absorption measurements were performed on a PerkinElmer Lambda 1050 UV/Vis/NIR spectrometer (PerkinElmer, Santa Clara, CA), equipped with a Peltier temperature control accessory. Zeta potential of nanomaterials was measured using Zetasizer nano (Malvern Panalytical, UK). Fluorescence spectra were obtained with an RF-6000 spectrophotometer (Shimadzu, Japan). Transmission electron microscopy (TEM) images of GO and AuNPs were taken using a Hitachi 7500 transmission electron microscope (Hitachi, Japan). All ICP-MS measurements were carried out using a Thermo Scientific iCAP Qc ICP-MS (Bremen, Germany) coupled with a 4-channel 12-roller peristaltic pump, nickel sample and skimmer cones, a Teledyne CETAC ASX560 autosampler (Omaha, NE), a microflow perfluoroalkoxy nebulizer (Thermo Scientific) and a Peltier-cooled quartz cyclonic spray chamber. To monitor the ICP-MS instrument, the THERMO-4AREV (Thermo Scientific) standard was run daily for maximum 59Co, 238U and minimum 140Ce16O/140Ce signal. The ICP-MS measurements of AuNPs were controlled by the Qtegra™ software (version 2.8.2944.202). The instrument operating parameters used for the single particle and conventional ICP-MS measurements are listed in Table S1 (Supporting Information).
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3

Analytical Characterization of Anabolic Steroids

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The anabolic steroid analytes, buffer chemicals, Rhodamine 6G, tetrahydrofuran (THF), and dimethyl sulfoxide (DMSO)-d6 were obtained from Sigma-Aldrich Chemical Company and the cyclodextrins were obtained from Tokyo Chemical Industry. All chemicals were used as received. All fluorescence measurements were performed using a Shimadzu RF 6000 spectrophotometer. The excitation and emission slit widths were set to 3.0 nm. All fluorescence spectra were integrated vs. wavenumber on the X-axis using OriginPro 2019 Version 9.60. All arrays were generated using SYSTAT Version 13.1. NMR studies were conducted using a Bruker 400 MHz NMR spectrometer and spectra were analyzed using MestReNova 14.1 software. Electrostatic potential map models were generated using Spartan' 18 software.
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4

Comprehensive Characterization of Photoluminescent Graphene Quantum Dots

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A PerkinElmer Lambda 1050 UV-250 UV/vis/NIR
spectrophotometer was used for the UV–vis absorption measurements
of the PGQDs. The fluorescence spectra and photostability measurements
were acquired by a Shimadzu RF-6000 spectrophotometer. A Malvern model
of Nano-ZS Zetasizer was used to measure size distribution of the
PGQDs as well as the zeta potential at various pHs. A Thermo Fisher
Scientific Nicolet iS5 Fourier transform infrared spectrometer (FT-IR)
was utilized to obtain the IR spectra of PGQDs, TCPP, CBDA-2, and
the GQDs. A Hitachi 7500 Transmission Electron Microscope (TEM) and
a JEOL JEM-F200 High-Resolution Transmission Electron Microscope (HRTEM)
were used for particle imaging. Powder X-ray diffraction (XRD) measurement
was conducted on a Rigaku SmartLab X-ray diffractometer at a scan
rate of 4°/min with Cu Kα irradiation (λ = 0.15418)
at an accelerating voltage of 40 kV and a tube current of 44 mA. The
fine powder sample was loaded on a zero-background silicon wafer sample
holder. An Olympus FV1000 MPE Basic Multiphoton Microscope was used
for in vitro confocal imaging. HeLa cells were cultured
overnight with gradient concentrations of the PGQDs for in
vitro
imaging and cytotoxicity analysis. A ELX800 plate reader
was used for the cell viability experiments using the protocol of
CytoTox 96 Non-Radioactive Cytotoxicity Assay kit.
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5

Characterization of GQDs-hMSNs Nanocomposite

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A Hitachi 7500 transmission electron microscope (TEM) was used to image the GQDs-hMSNs. A Malvern model of Nano-ZS Zetasizer was used to measure size distribution and the zeta potential. UV-Vis absorption was analyzed by a Perkin Elmer Lambda 1050 UV-250 UV/Vis/NIR spectrophotometer and the fluorescence spectra was acquired by a Shimadzu RF-6000 spectrophotometer. IR spectra of hMSNs, GQDs, and GQDs-hMSNs were collected on a Thermo Fisher Scientific Nicolet iS5 Fourier transform infrared spectrometer (FT-IR). A Benchmark MultiThermal (Cool—Heat—Shake) H5000-H vortex system was used to integrate of GQDs into the hMSNs. A PHI Model 10-360 electron spectrometer with non-monochromatized Al Kα (1486.3 eV) X-rays was used for X-ray photoelectron spectroscopy (XPS). An Olympus FV3000 Laser Scanning Confocal Microscope was used for the in vitro cell imaging of the GQDs-hMSNs with two channels being used for imaging: red (Fura-Red (Ca-free)) and green (Alexa 488).
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6

Optical Absorption and Emission of CsPbBr3 QDs

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Optical absorption spectra in the UV–visible range were obtained using a Shimadzu UV-1800 spectrophotometer (Kyoto, Japan), which was operated with UVProbe 2.52 software. Concurrently, the emission characteristics were assessed through steady-state photoluminescence (PL) spectra, recorded using a Shimadzu RF-6000 spectrophotometer (Kyoto, Japan) equipped with LabSolutions RF software (1.11). For CsPbBr3, the excitation wavelength (λex) utilized was 400 nm. The preparation for optical evaluation involved the dilution of quantum dot (QD) solutions in n-hexane, followed by their allocation into quartz cuvettes, each with a path length of 10 mm, to ensure accurate measurements.
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7

Synthesis and Characterization of Losartan-Zinc(II) Complex

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All chemicals were of analytical grade and used without further purification. Losartan, potassium salt was purchased from Parafarm and Zinc(II) nitrate (Merck) was used as supplied. A sodium silicate solution (14% NaOH-27% SiO 2 , SiO 2 .NaOH, Sigma-Aldrich) was used for the diffusion method. Infrared spectra of powdered samples were measured with a Bruker IFS 66 FTIR-spectrophotometer from 4000 to 400 cm -1 using the KBr pellet technique. FT-Raman spectra were measured using the FRA 106 Raman accessory with germanium detector operating at liquid nitrogen temperature. A continuouswave Nd/YAG laser working at 1064 nm was employed for Raman excitation. Elemental analyses for carbon, hydrogen and nitrogen were performed using a Carlo Erba EA 1108 analyzer. Thermogravimetric analysis (TGA) were measured with a Shimadzu system (model TG-50), working in an oxygen flow of 50 mL/min and at a heating rate of 10 °C/min. Sample quantities ranged between 5 and 10 mg. Electronic absorption spectra were recorded on a Hewlett-Packard 8453 diode-array spectrophotometer, using 1-cm quartz cells. Fluorescence spectra were measured using a Shimadzu RF-6000 spectrophotometer. The molar conductance of the complex was measured on a Conductivity TDS Probe -850,084, Sper Scientific Direct, using 10
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