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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

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A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
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Author Spotlight: High-Quality Quantum Dot Nanobeads for Sensitive Fluorescent Lateral Flow Immunoassays
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Fluorogenic enzyme-linked immunosorbent assay with a dual color variation.

Hanool Yun1, Hee-Jin Jeong1

  • 1Department of Biological and Chemical Engineering, Hongik University, 2639 Sejong-ro, Sejong-si 30016, South Korea.

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|January 31, 2024
PubMed
Summary

A new fluorogenic enzyme-linked immunosorbent assay (FELISA) enables sensitive detection of tumor necrosis factor alpha (TNFα) and programmed cell death-ligand 1 (PDL1). This high-throughput method offers rapid and accurate biomarker analysis for disease diagnosis and treatment.

Keywords:
Fluorescent biosensorFluorogenic enzyme-linked immunosorbent assayImmunoassayProgrammed cell death-ligand 1Tumor necrosis factor alpha

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Area of Science:

  • Biochemistry
  • Immunology
  • Assay Development

Background:

  • Accurate biomarker detection is vital for disease diagnosis, monitoring, and treatment.
  • Existing immunoassay tools may lack the required sensitivity or throughput for certain applications.

Purpose of the Study:

  • To develop a sensitive and high-throughput fluorogenic enzyme-linked immunosorbent assay (FELISA).
  • To detect key biomarkers: tumor necrosis factor alpha (TNFα) and programmed cell death-ligand 1 (PDL1).

Main Methods:

  • Development of a FELISA utilizing Amplex Red or QuantaBlu fluorescent substrates.
  • Application of the assay for the detection of TNFα and PDL1.

Main Results:

  • Achieved a limit of detection in the nanogram order for TNFα and PDL1.
  • Enabled convenient assaying of multiple samples within 20 hours.
  • Demonstrated FELISA's applicability as a powerful immunoassay tool.

Conclusions:

  • FELISA provides a rapid and accurate method for detecting TNFα and PDL1.
  • This assay platform is versatile and can be adapted for various fluorogenic immunoassays against other antigens.