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Related Concept Videos

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,...
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...
Electrophoresis: Overview01:20

Electrophoresis: Overview

Electrophoresis is a powerful analytical separation technique that relies on the differential migration of charged species when subjected to an electric field. The core strength of electrophoresis lies in its ability to separate high-molecular-weight species in complex mixtures. It has found widespread use in biochemistry, molecular biology, and analytical chemistry, allowing the separation of compounds like amino acids, nucleotides, carbohydrates, and proteins with excellent resolution.
There...
Capillary Electrophoresis: Instrumentation01:20

Capillary Electrophoresis: Instrumentation

Capillary electrophoresis instrumentation typically consists of several key components. A high-voltage power supply generates the electric field necessary for the separation by connecting to an anode (the positively charged electrode) and a cathode (the negatively charged electrode) located in buffer reservoirs at each end of the capillary tube. The system includes a sample vial, a fused silica capillary tube coated with polyimide for mechanical strength through which the sample components...
SDS-PAGE01:27

SDS-PAGE

Gel electrophoresis is a method that separates biological macromolecules like nucleic acids or proteins by forcing them to pass through a gel matrix under an electric field.
A variation of gel electrophoresis, termed  polyacrylamide gel electrophoresis (PAGE), is commonly used for separating proteins according to their molecular size by passing them through a polyacrylamide gel. Because of the varying charges associated with amino acid side chains, PAGE can be used to separate intact proteins...

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Related Experiment Video

Updated: Jul 9, 2026

Electrophoretic Separation of Proteins
08:17

Electrophoretic Separation of Proteins

Published on: June 12, 2008

Recent innovations in protein separation on microchips by electrophoretic methods.

Youyuan Peng1, Antoine Pallandre, N Thuy Tran

  • 1University Paris-Sud, Laboratory of Proteins and Nanotechnologies in Separation Sciences, Châtenay-Malabry, France.

Electrophoresis
|December 7, 2007
PubMed
Summary

This review highlights recent advancements in microchips for capillary electrophoresis (CE) protein separation. Microchip CE offers powerful analytical capabilities for biological, pharmaceutical, and food analysis.

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Last Updated: Jul 9, 2026

Electrophoretic Separation of Proteins
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10:55

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Area of Science:

  • Analytical Chemistry
  • Biotechnology
  • Separation Science

Background:

  • Microchips for analytical purposes have gained significant attention over the past two decades.
  • Capillary electrophoresis (CE) on microchip platforms is a rapidly developing field.

Purpose of the Study:

  • To review recent developments in microchips for electrophoretic separation of proteins.
  • To cover basic microchip layout for CE, commercial platforms, and surface treatments.

Main Methods:

  • Discussion of on-line sample pretreatment strategies for protein pre-concentration and purification.
  • Adaptation of common CE modes to chip format, with ongoing progress in multidimensional approaches.
  • Overview of detection methods, including derivatization and labeling of proteins.

Main Results:

  • Microchip CE platforms are increasingly sophisticated for protein analysis.
  • On-chip sample pretreatment enhances protein analysis efficiency.
  • Various detection strategies are employed for sensitive protein identification.

Conclusions:

  • Microchip CE demonstrates significant potential for protein separations in diverse fields.
  • Applications span biological, pharmaceutical, agricultural, and food analysis.
  • The review covers literature from 2000 to early 2007, with 151 references.