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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or quantified.
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Photoluminescence: Applications01:14

Photoluminescence: Applications

Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...

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Related Experiment Video

Updated: Jun 14, 2026

High-throughput Fluorometric Measurement of Potential Soil Extracellular Enzyme Activities
12:33

High-throughput Fluorometric Measurement of Potential Soil Extracellular Enzyme Activities

Published on: November 15, 2013

[Recent advances in enzyme assays using fluoremetry].

Yanlong Xing1, Xiangzhao Mao, Shu Wang

  • 1Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Science, Qingdao 266101, China.

Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology
|April 1, 2010
PubMed
Summary
This summary is machine-generated.

Fluorescent probes offer sensitive and dynamic monitoring for enzyme assays, crucial for bio-engineering, disease diagnosis, and drug discovery. This review covers recent advances and applications of these powerful tools.

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Last Updated: Jun 14, 2026

High-throughput Fluorometric Measurement of Potential Soil Extracellular Enzyme Activities
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Published on: November 15, 2013

Multi-enzyme Screening Using a High-throughput Genetic Enzyme Screening System
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Published on: August 8, 2016

Use of Recombinant Fusion Proteins in a Fluorescent Protease Assay Platform and Their In-gel Renaturation
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Area of Science:

  • Biochemistry and Molecular Biology
  • Analytical Chemistry

Context:

  • Enzyme assays are critical tools in various scientific and medical fields.
  • Fluorescence-based detection methods are gaining prominence due to their high sensitivity and dynamic monitoring capabilities.

Purpose:

  • To review recent advancements and applications of fluorescent probes in enzyme assays.
  • To classify different fluorescence detection methods based on substrates and mechanisms.
  • To provide an overview of available tools and strategies for enzyme assays using fluorescent probes.

Summary:

  • This review categorizes enzyme assay methods using fluorescent probes into direct and indirect detection.
  • It highlights the advantages of fluorometry, including sensitivity and real-time monitoring.
  • The discussion encompasses current research trends and future prospects in the field.

Impact:

  • Facilitates the development of novel diagnostic tools for diseases.
  • Supports advancements in drug discovery and development pipelines.
  • Provides researchers with a comprehensive understanding of fluorescent probe applications in enzyme analysis.