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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.
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Immunoprecipitation, or IP, is a widely used technique that employs protein-antibody interactions to isolate proteins or protein complexes in their native state for studying protein-protein interactions, quaternary structures, or supramolecular complexes. Various modifications of the technique, including chromatin IP, cross-linking IP, and fluorescence IP, are commonly used.
Chromatin Immunoprecipitation
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A Simple Method for Automated Solid Phase Extraction of Water Samples for Immunological Analysis of Small Pollutants
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Published on: January 1, 2016

Flow immunoassay using solid-phase entrapment.

L Locascio-Brown1, L Martynova, R G Christensen

  • 1National Institute of Standards and Technology, Gaithersburg, Maryland 20899.

Analytical Chemistry
|May 31, 2011
PubMed
Summary
This summary is machine-generated.

This study presents a rapid flow injection immunoassay for phenytoin detection. The simple, 2-minute assay reliably measures anticonvulsant drug levels in serum with a low detection limit.

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Area of Science:

  • Analytical Chemistry
  • Biochemistry
  • Immunochemistry

Background:

  • Accurate quantification of anticonvulsant drugs is crucial for therapeutic drug monitoring.
  • Traditional immunoassays can be time-consuming and complex.

Purpose of the Study:

  • To develop a rapid and simple flow injection immunoassay for phenytoin.
  • To validate the assay's performance characteristics, including detection limit and assay time.

Main Methods:

  • A flow injection immunoassay utilizing a reversed-phase sorbent column for separation.
  • Competitive assay format using fluorescein-labeled analyte for phenytoin measurement.
  • Regeneration of the column using ethanol solutions for reusability.

Main Results:

  • Successful separation of immunoreacted species by entrapping free analyte.
  • Phenytoin measurement in serum with a reliable detection limit of 5 nmol/L.
  • Assay time reduced to a rapid 2 minutes per measurement.

Conclusions:

  • The developed flow injection immunoassay offers a simple, fast, and reliable method for phenytoin quantification.
  • This technique is suitable for therapeutic drug monitoring of anticonvulsant drugs.
  • The column's regenerability enhances the assay's cost-effectiveness and practicality.