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Related Concept Videos

Labeling DNA Probes03:31

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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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Updated: Jun 7, 2025

Multiplexed Barcoding Image Analysis for Immunoprofiling and Spatial Mapping Characterization in the Single-Cell Analysis of Paraffin Tissue Samples
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Simple generation of cleavable labels for multiplexed imaging.

Vincent Van Deuren1, Silke Denis1, Robin Van den Eynde1

  • 1Laboratory for Nanobiology, Department of Chemistry, KU Leuven, Leuven, Belgium. vincent.vandeuren@kuleuven.be.

Chemical Communications (Cambridge, England)
|November 18, 2024
PubMed
Summary
This summary is machine-generated.

This study introduces a simple, inexpensive method for amine-targeted antibody labeling using a cleavable linker. This technique facilitates efficient multiplexed immunohistochemistry and high-content imaging through easy label removal.

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Immunohistochemistry

Background:

  • Multiplexed immunohistochemistry commonly uses cyclic staining, imaging, and regeneration.
  • Existing methods can be complex and costly.

Purpose of the Study:

  • To develop a simple, inexpensive amine-targeted antibody labeling method.
  • To enable efficient cyclic staining-imaging-removal for multiplexed assays.

Main Methods:

  • Amine-targeted antibody labeling using a cleavable linker.
  • One-pot reaction with readily available reagents.
  • Demonstration on isolated cells and tissue sections.

Main Results:

  • Over 94% of labels removed in 30 minutes with mild reducing agent.
  • Up to 99% label removal achieved within 1 hour.
  • Method applicable to repeated staining-imaging-removal cycles.

Conclusions:

  • The developed method simplifies multiplexed immunohistochemistry and high-content imaging.
  • Introduces a convenient way to incorporate cleavable linkers.
  • Offers an accessible approach for researchers without synthetic experience.