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Cellroxs deep red reagent

Manufactured by Thermo Fisher Scientific
Sourced in United States

The CellROX Deep Red Reagent is a fluorogenic probe used to detect oxidative stress in live cells. The reagent becomes fluorescent upon oxidation, allowing for the measurement of reactive oxygen species (ROS) levels within the cellular environment.

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3 protocols using cellroxs deep red reagent

1

Intracellular ROS Generation Assay

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Intracellular reactive oxygen species (ROS) generation was evaluated by Cell ROXs Deep Red Reagent (Thermo Fisher Scientific, USA). Briefly, the cells grown in 96-well plates and treatment with 10 μM artemisinin for 2 h. After 2 h, media was removed and cells were exposed to 100 μM H2O2 for 24 h. Cells were then incubated with Cell ROXs Deep Red Reagent (5μM) in fresh DMEM for 1h in dark. Cells were washed with 1X PBS. The fluorescence was measured by fluorescence microscope with a high content screening system (ArrayScanVTI, Thermo FisherScientific, USA) at excitation 640 nm and the emission 665 nm wave length. ROS level was semi-quantified and percentage of ROS level was normalized with the control group.
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2

Quantifying Intracellular ROS Levels

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Intracellular reactive oxygen species (ROS) levels were assessed by CellROXs Deep Red Reagent (Thermo Fisher Scientific, USA), according to the commonly used protocols in our laboratory [24 (link)]. Briefly, cells grown in 96-well plates were incubated with 1 μM Aβ1-42 with or without pretreatment with different concentrations of Artemether. Cells were then incubated with CellROXs Deep Red Reagent (5 μM in fresh DMEM for 1 hour in the dark). Fluorescence was measured, and semiquantitative ROS levels and normalized ROS levels are presented as a percentage of the control group.
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3

Intracellular ROS Measurement in PC12 Cells

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Intracellular ROS generation was assessed using CellROXs Deep Red Reagent (Thermo Fisher Scientific, USA). After appropriate treatment,the PC12 cells were incubated with CellROXs Deep Red Reagent (5 mM) in DMEM for 1 h in the dark, rinsed twice with 1x PBS solution and the fluorescence was observed and recorded using a fluorescent micro-scope at an excitation wavelength of 640 nm and an emission wavelength of 665 nm. Semiquantification of ROS level was evaluated by using Image-J software. All values of % ROS level were normalized to the control group.
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