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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
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Related Experiment Video

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Application of Genetically Encoded Fluorescent Nitric Oxide (NO&#8226;) Probes, the geNOps, for Real-time Imaging of NO&#8226; Signals in Single Cells
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A new H2Se-selective fluorescent probe based on nitro reduction.

Wenfang Liang1, Liyue Wang2, Zhili Yu3

  • 1College of Chemical Engineering, Beijing University of Chemical Technology (BUCT), Beijing 100029, China. yilong@mail.buct.edu.cn.

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|October 4, 2025
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Summary
This summary is machine-generated.

Researchers developed a new probe, Nap-NO2-mCl, for highly selective detection of hydrogen selenide (H2Se) in biological systems. This tool enables effective monitoring of H2Se in living cells.

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Area of Science:

  • Biochemistry
  • Chemical Biology
  • Molecular Biology

Background:

  • Hydrogen selenide (H2Se) is recognized as a bioactive molecule involved in various physiological and pathological conditions.
  • Accurate detection of H2Se is crucial for understanding its biological roles.

Purpose of the Study:

  • To develop a highly selective and sensitive detection tool for hydrogen selenide (H2Se).
  • To investigate the utility of the developed probe in monitoring H2Se in biological contexts.

Main Methods:

  • Rational design of H2Se probes utilizing nitroaromatic reduction and self-immolative processes.
  • Synthesis and characterization of the Nap-NO2-mCl probe.
  • Evaluation of probe selectivity, sensitivity, and performance in detecting H2Se in living cells.

Main Results:

  • A novel H2Se detection platform, Nap-NO2-mCl, was successfully developed.
  • The Nap-NO2-mCl probe demonstrated high selectivity and sensitivity towards H2Se.
  • The probe effectively monitored both triggered-release and exogenous H2Se in living cells.

Conclusions:

  • The Nap-NO2-mCl probe represents a valuable tool for H2Se detection in biological research.
  • This platform facilitates further investigation into the physiological and pathological functions of H2Se.