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Updated: May 22, 2026

Correlative Light- and Electron Microscopy Using Quantum Dot Nanoparticles
Published on: August 7, 2016
[Imaging of surface cell antigens on the tumor sections of lymph nodes using fluorescence quantum dots]
Insights
Quantum dots offer stable, specific detection of lymphoid cell antigens. This method enhances immunofluorescence microscopy for diagnostic coexpression analysis.
Area of Science:
- Immunology
- Biotechnology
- Materials Science
Context:
- Quantum dots (QDs) are semiconductor nanocrystals with unique optical properties.
- Immunofluorescence is a technique used to detect antigens in biological tissues.
- Lymphoid cells are crucial components of the immune system.
Purpose:
- To evaluate the utility of quantum dots for immunofluorescent detection of surface antigens on lymphoid cells.
- To optimize quantum dot detection through upgrading fluorescent microscopy.
- To assess the stability, specificity, and sensitivity of quantum dot-based immunofluorescence.
Summary:
- Upgraded fluorescent microscopy enabled multi-QD imaging from single sections, enhancing quantum dot detection.
- QD-stained specimens showed stability for over two weeks and minimal photobleaching.
- Direct conjugates of monoclonal antibodies with QDs exhibited high specificity and sensitivity for double staining on frozen sections.
- Minimal spectral spillover (≤8%) between QDs with 40 nm spectral separation reduces the need for compensation.
Impact:
- This QD-based immunofluorescence method provides a stable and sensitive approach for analyzing antigen coexpression in lymphoid tissues.
- The technique supports diagnostic purposes by enabling reliable antigen analysis.
- The high photostability and minimal spectral overlap of QDs offer advantages over traditional fluorescent dyes.
Abstract:
The usefulness of quantum dots for the immunofluorescent detection of surface antigens on the lymphoid cells has been studied. To optimize quantum dots detection we have upgraded fluorescent microscope that allows obtaining multiple images from different quantum dots from one section. Specimens stained with quantum dots remained stable over two weeks and practically did not bleach under mercury lamp illumination during tens of minutes. Direct conjugates of primary mouse monoclonal antibodies with quantum dots demonstrated high specificity and sufficient sensitivity in the case of double staining on the frozen sections. Because of the high stability of quantum dots' fluorescence, this method allows to analyze antigen coexpression on the lymphoid tissue sections for diagnostic purposes. The spillover of fluorescent signals from quantum dots into adjacent fluorescent channels, with maxima differing by 40 nm, did not exceed 8%, which makes the spectral compensation is practically unnecessary.

