ARG81192

Intracellular ROS Assay Kit (Fluorometric)

Intracellular ROS Assay Kit (Fluorometric) for Functional study and All

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Overview

Tested Reactivity All
Tested Application FuncSt
Target Name ROS
Conjugation Un-conjugated
Conjugation Note Read the fluorescence with a fluorescence plate reader at 480 nm excitation / 530 nm emission.
Sensitivity 0.01 nM
Sample Type Cultured cells
Standard Range 0.01 - 10000 nM
Sample Volume Cultured cells in either a clear or black 96-well cell culture plate.

Application Instructions

Assay Time ~ 1 hour

Properties

Form Liquid
Storage Instruction Store components at 4°C or -20°C. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Background In chemistry and biology, reactive oxygen species (ROS) are highly reactive chemicals formed from diatomic oxygen (O2), water, and hydrogen peroxide. Some prominent ROS are hydroperoxide (O2H), superoxide (O2-), hydroxyl radical (OH.), and singlet oxygen. ROS are pervasive because they are readily produced from O2, which is abundant. ROS are important in many ways, both beneficial and otherwise. ROS function as signals, that turn on and off biological functions. They are intermediates in the redox behavior of O2, which is central to fuel cells. ROS are central to the photodegradation of organic pollutants in the atmosphere. Most often however, ROS are discussed in a biological context, ranging from their effects on aging and their role in causing dangerous genetic mutations.[Wikipedia]

Images (3) Click the Picture to Zoom In

  • ARG81192 Intracellular ROS Assay Kit (Fluorometric) standard curve image

    ARG81192 Intracellular ROS Assay Kit (Fluorometric) results of a typical standard run with optical density reading at 480 nm excitation / 530 nm emission.

  • ROS in HeLa cells treated with H2O2

    50,000 HeLa cells in a 96-well plate were first pretreated with 1 mM DCFH-DA for 60 minutes at 37°C. Cells were then treated with various concentrations of H2O2 for 20 minutes.

  • DCF Fluorescence in HeLa cells treated with H2O2

    DCF Fluorescence in H2O2 treated HeLa cells after 1 hour. Left: 0 µM; Right: 1000 µM.

Specific References

TNFAIP3 interacting protein 2 relieves lipopolysaccharide (LPS)-induced inflammatory injury in endometritis by inhibiting NF-kappaB activation

FuncSt / Human

Xinxin Qian et al.
Immun Inflamm Dis.,  (2023)

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