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S 1700

Manufactured by Shimadzu
Sourced in Japan

The S-1700 is a high-performance UV-Vis spectrophotometer designed for accurate and reliable absorbance measurements across a wide range of applications. It features a compact and durable construction, making it suitable for use in various laboratory settings.

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6 protocols using s 1700

1

Turbidimetric Analysis of Thermal Transitions

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Turbidimetry experiments were performed on UV/vis spectrophotometer (UV2550 Shimadzu) equipped with a temperature controller (S-1700) at 670 nm wavelength. Purified samples were dissolved in polypropylene tubes for two hours at 60 °C to obtain 1 wt% solutions. The cuvette and the cuvette holder were heated to 50 °C, the sample was quickly transferred to the cuvette and the measurement of the cooling curve was performed from 50 °C to 3 °C at the rate of 1 °C min−1 with 10 s wait time before each transmittance acquisition. The sample was kept at 3 °C for 5 min before proceeding with the heating cycle measurement from 3 to 50 °C under the same conditions as for the cooling cycle. The sample was constantly stirred during the measurement. The cloud point was determined as the inflection point of the transmittance curve.
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2

Characterization of Upconversion Nanoparticles

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Sizes and morphologies were determined at 200 kV using a JEOL JEM-2010F high-resolution transmission electron microscope (HR-TEM). Energy-dispersive X-ray analysis (EDXA) was also performed during HR-TEM measurements. Dynamic light scattering experiments were carried out on a Zetasizernano 90. Powder X-ray diffraction (XRD) measurement was measured with a Bruker D4 X-ray diffractometer (Cu Kα radiation, 0.15406 nm). Upconversion luminescence (UCL) spectra were measured with a Maya LIFS-980 fluorescence spectrometer by using an external 0-5 W 980 nm adjustable laser as the excitation source. Ultraviolet-visible-near infrared (UV-vis-NIR) absorption spectra were obtained using a UV-2550 spectrophotometer (S-1700, Shimadzu, Japan). Fourier transform infrared (FTIR) spectra were performed on Fourier Transform Infrared Spectrophotometer IRPRESTIGE-21 (Shimadzu) .
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3

Quantifying Reactive Oxygen Species Generation

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All chemicals were used as received. ·OH was generated by the Fenton reaction.36 (link)1O2 was generated from the H2O2/MoO42− system in alkaline media.37 (link) NO was generated using sodium nitroferricyanide(iii) dehydrate.38 (link) ONOO was generated from the SIN-1 reagent (Dojindo Molecular Technologies, Japan). ·O2 was generated using potassium superoxide (KO2).36 (link) Fluorescence spectra were measured on a JASCO FP-6500 fluorescence spectrophotometer with a 10 nm path length cell (both excitation and emission slit widths, 5.0 nm) at 298 ± 1 K using a temperature controller.39 (link) Absorption spectra were measured on an UV-visible photodiode-array spectrometer (Shimadzu; Multispec-1500) equipped with a temperature controller (S-1700).40 (link) All measurements were performed under aerated conditions. 1H and 13C NMR charts were obtained using a JEOL JNM-ECS400 spectrometer. FAB-MS analysis was performed on a JEOL JMS 700 Mass Spectrometer. Fluorescence quantum yields (ΦF) were determined with quinine sulfate dihydrate (in 0.1 M HClO4 solution) as a standard.41,42 (link)
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4

LCST Characterization of P2 and P3

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The LCST of P2 and P3 was characterized at a concentration of 1 mg mL−1 by 50% of the maximum absorbance at 600 nm. The UV-vis spectra of P2 and P3 were obtained using a UV/Vis spectrophotometer (Shimadzu 3600) with a thermoelectric single cell holder (S-1700). A thermoelectric temperature controller was used to control the sample temperature.
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5

Melting Curve Analysis of DNA Duplexes

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UV absorbance versus temperature melting curves were measured at 260 nm to acquire the Tm of various duplexes on a UV-2550 spectrophotometer (SHIMADZU, Kyoto, Japan) equipped with a S-1700 temperature controller [27 (link)]. The cell was sealed to avoid solvent evaporation and a magnetic stick was used to dispose of the gas bubbles generated in heating course. Each DNA sample at a concentration of 40 µM was dissolved in 50 mM KOAc at pH 4.5 or 9.0. In each step, the temperature was increased by 1°C and equilibrated for 3 min before recording the absorbance.
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6

UV Melting Curve Analysis of Biomolecules

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UV melting curves were recorded on a UV-2550 spectrophotometer (SHIMADZU, Kyoto, Japan) fitted with an S-1700 temperature controller measured at 295 nm as in previous reports [24 (link),25 ]. The temperature was increased at a heating rate of 0.5°C min with DNA samples being left to equilibrate for 0.5 min at each temperature. The absorption cell was sealed to prevent solvent evaporation, and the bubble was removed by stirring during the heating process.
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