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Jes re1x x band spectrometer

Manufactured by JEOL
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Sourced in Japan

The JES-RE1X is an X-band spectrometer manufactured by JEOL. It is designed for electron paramagnetic resonance (EPR) spectroscopy, a technique used to study the properties of materials with unpaired electrons. The spectrometer operates at a frequency of approximately 9.5 GHz and is capable of detecting and analyzing the magnetic properties of these unpaired electrons.

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Lab products found in correlation

J 720 spectropolarimeter, by Jasco (1 mentions) V 560 spectrometer, by Jasco (1 mentions)

Spelling variants of this product

JES-RE1X (7 citations) JES-RE1X spectrometer (3 citations) -RE1X spectrometer (2 citations)

2 protocols using jes re1x x band spectrometer

1

Spectroscopic Characterization of Biomolecules

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Absorption spectra have been measured on a Shimadzu UV-2600 spectrometer or on a JASCO V-560 spectrometer, to both of which a temperature controller has been attached, using quartz cells with 1 mm or 10 mm path-length. Circular dichroism (CD) spectra have been measured on a JASCO J-720 spectropolarimeter. Electron paramagnetic resonance (EPR) spectrum has been measured on a JEOL JES-RE1X X-band spectrometer at 77 K.
Widiatningrum T., Maeda S., Kataoka K, & Sakurai T. (2015). A pirin-like protein from Pseudomonas stutzeri and its quercetinase activity. Biochemistry and Biophysics Reports, 3, 144-149.
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2

ROS Generation Measurement via ESR

Cited 1 time
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ROS generation in cells was measured using ESR, as previously described (19 (link)). Briefly, 106 cells were seeded on a glass cover slide (49.0×5.0×0.2 mm) and incubated overnight as previously described. Cells were treated with 0 or 1,000 µM TP4O for 15 min. ESR was measured in a respiration buffer containing 10 mM DMPO as the spin-trapping agent. All ESR spectra were obtained using a JES-RE1X X-band spectrometer (JEOL, Ltd., Tokyo, Japan).
Nakayama K., Murata S., Ito H., Iwasaki K., Villareal M.O., Zheng Y.W., Matsui H., Isoda H, & Ohkohchi N. (2017). Terpinen-4-ol inhibits colorectal cancer growth via reactive oxygen species. Oncology Letters, 14(2), 2015-2024.
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