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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.
Immunogold Electron Microscopy01:20

Immunogold Electron Microscopy

Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
Immunoprecipitation01:20

Immunoprecipitation

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
Chromatin immunoprecipitation, also known as ChIP, is used to study protein-DNA or...
Two-dimensional Gel Electrophoresis01:22

Two-dimensional Gel Electrophoresis

Two-dimensional gel electrophoresis is a high-resolution protein separation method first introduced by O' Farrell and Klose in 1975. This method involves protein separation by two dimensions, mass and charge, making it more accurate than one-dimensional gel electrophoresis.
The first dimension separation uses the isoelectric focusing or IEF technique performed on immobilized pH gradient (IPG) strips that separate proteins according to their isoelectric points.
Biological samples, such as  cells...
Capillary Electrophoresis: Applications01:30

Capillary Electrophoresis: Applications

Capillary electrophoretic separations offer various modes, each with unique applications. These modes include capillary zone electrophoresis, capillary gel electrophoresis, capillary array electrophoresis, capillary isoelectric focusing, capillary isotachophoresis, micellar electrokinetic chromatography, and capillary electrochromatography.
Capillary zone electrophoresis (CZE) separates ionic components based on their electrophoretic mobility. It has been used to separate proteins, amino acids,...
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...

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Related Experiment Video

Updated: May 16, 2026

Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay
06:15

Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay

Published on: September 7, 2018

Rocket immunoelectrophoresis technique or electroimmunodiffusion.

A Laine1

  • 1INSERM, Lille Cedex, France.

Methods in Molecular Biology (Clifton, N.J.)
|November 15, 2012
PubMed
Summary

Rocket immunoelectrophoresis (electroimmunodiffusion) offers a simple, fast method for quantifying single proteins or proteins within mixtures. Accurate results depend on identical physicochemical and immunological properties between samples and references.

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Highly Sensitive and Quantitative Detection of Proteins and Their Isoforms by Capillary Isoelectric Focusing Method
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Highly Sensitive and Quantitative Detection of Proteins and Their Isoforms by Capillary Isoelectric Focusing Method

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Procedure and Key Optimization Strategies for an Automated Capillary Electrophoretic-based Immunoassay Method
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Procedure and Key Optimization Strategies for an Automated Capillary Electrophoretic-based Immunoassay Method

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Related Experiment Videos

Last Updated: May 16, 2026

Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay
06:15

Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay

Published on: September 7, 2018

Highly Sensitive and Quantitative Detection of Proteins and Their Isoforms by Capillary Isoelectric Focusing Method
07:58

Highly Sensitive and Quantitative Detection of Proteins and Their Isoforms by Capillary Isoelectric Focusing Method

Published on: September 19, 2018

Procedure and Key Optimization Strategies for an Automated Capillary Electrophoretic-based Immunoassay Method
09:32

Procedure and Key Optimization Strategies for an Automated Capillary Electrophoretic-based Immunoassay Method

Published on: September 10, 2017

Area of Science:

  • Biochemistry
  • Immunology
  • Analytical Chemistry

Background:

  • Quantifying specific proteins is crucial in various scientific fields.
  • Existing methods may lack speed, simplicity, or reproducibility.
  • Rocket immunoelectrophoresis (electroimmunodiffusion) presents an alternative technique.

Purpose of the Study:

  • To describe the rocket immunoelectrophoresis (electroimmunodiffusion) technique.
  • To highlight its applicability for single protein quantitation and analysis within mixtures.
  • To emphasize its speed, simplicity, and reproducibility.

Main Methods:

  • Utilizes rocket immunoelectrophoresis (electroimmunodiffusion) on agarose gel plates.
  • Incorporates monospecific antiserum within the agarose gel.
  • Employs one-dimensional electrophoresis to form rocket-shaped precipitates.
  • Quantification is achieved by measuring the height of these precipitate peaks.

Main Results:

  • The technique allows for the analysis of multiple unknown samples on a single plate.
  • Accurate quantitation requires physicochemical and immunological identity between samples and reference solutions.
  • Rocket-shaped precipitates are formed, enabling direct measurement.

Conclusions:

  • Rocket immunoelectrophoresis (electroimmunodiffusion) is a valuable tool for protein quantitation.
  • The method is efficient for both single proteins and complex mixtures.
  • Its simplicity and speed make it suitable for routine analysis.