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Fluoromax 4

Manufactured by Shimadzu

The FluoroMax-4 is a high-performance spectrofluorometer designed for accurate and sensitive fluorescence measurements. It features a xenon lamp source, double-grating monochromators, and a photomultiplier tube detector to provide reliable and reproducible results. The core function of the FluoroMax-4 is to measure the fluorescence emission and excitation spectra of liquid and solid samples.

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3 protocols using fluoromax 4

1

Comprehensive Characterization of Carbon Dots

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An X-ray diffractometer
[Ultima IV Rigaku, USA, 18 kW with the rotating anode source Cu Kα1 line (λ = 1.54 Å)] was used to identify
the crystal structure of CDs. Raman spectra [MRS-320 Raman Instrument
system (Horiba Ltd, Japan)] identified the molecular interaction of
CDs at an excitation wavelength of 532 nm. A Fourier transform infrared
spectrophotometer [model IR Tracer-100 (Shimadzu, Japan)] was used
to analyze the functional groups of CDs with the wavenumber ranging
from 4000 to 400 cm–1 using the potassium bromide
(KBr) pellet technique. A X-ray photoelectron spectrometer [Escalab
250Xi spectrometer with an Al Kα radiation (hυ = 1486.6
eV)] determined the composition of CDs. A spectrofluorometer (FluoroMax-4)
and a UV–vis spectrophotometer (Shimadzu UV-1800) were used
to measure fluorescence and absorbance spectra, respectively. The
PL of the HA CDs was measured comparatively by referring to rhodamine
6G [R6G, QY (95%)]; the % QY of HA CDs was determined by the following
equation where I, A, and η are the integral PL intensity,
UV absorbance and the
optical density, and solvent reflective index, respectively.
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2

Thioflavin T Fluorescence Assay for Growth Hormone Aggregation

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Aliquots of GH solutions were diluted in 5% D-Mannitol into 200 μl in such a way that the final concentration of GH was of 12.5 μM. The solution was mixed with 2 μl of 2 mM ThT prepared in 20 mM Tris HCl, pH 8.0. ThT fluorescence was measured immediately after addition of ThT. The fluorescence experiment was carried out either on Horiba-JY (Fluoromax 4) or Shimadzu RF5301 PC, with excitation at 450 nm and emission in the range of 460–500 nm. The slit width for both excitation and emission was kept at 5 nm. The fluorescence intensity values at 482 nm were plotted. The fluorescence signals of all samples were normalized against that of GH + Zn(II) aggregates incubated for 15 days, which was set as 1. Three independent experiments were performed for each sample.
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3

Fluorescent Dye Characterization

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Fluorescence and UV-Vis measurements were taken at a concentration of 0.1 mg/mL using a Fluoromax-4 (slit width 2 nm) and a Shimadzu UV-1601 UV/vis spectrometer, respectively. For fluorescein conjugates an excitation of 491 nm and emission of 521 nm was employed. For TAMRA conjugates an excitation of 560 nm and emission of 580 nm was employed.
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