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Related Concept Videos

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...
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,...
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: Jun 19, 2026

Immunostaining-Based Detection of Dynamic Alterations in Red Blood Cell Proteins
10:07

Immunostaining-Based Detection of Dynamic Alterations in Red Blood Cell Proteins

Published on: March 17, 2023

ELECTROPHORETIC STUDIES ON HUMAN RED BLOOD CELLS.

R F Furchgott1, E Ponder

  • 1The Biological Laboratory, Cold Spring Barber, Long Island.

The Journal of General Physiology
|October 30, 2009
PubMed
Summary

Human red blood cell surface properties change below an ionic strength of 0.02. Electrophoretic mobility data suggest the red cell surface is primarily lipid-based with dominant strong acid groups.

Area of Science:

  • Biophysics
  • Cell Biology
  • Biochemistry

Background:

  • Understanding red blood cell surface properties is crucial for hematology and disease diagnosis.
  • Electrophoretic mobility is a key indicator of cell surface charge and behavior.

Purpose of the Study:

  • To investigate the electrophoretic mobility of human red blood cells.
  • To determine how ionic strength and pH affect red cell surface characteristics.
  • To elucidate the composition of the red blood cell surface.

Main Methods:

  • Electrophoretic mobility measurements of human red blood cells.
  • Varying ionic strength and pH conditions.
  • Analysis of lipid and stroma protein extracts.

Main Results:

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Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry

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Antigens Protected Functional Red Blood Cells By The Membrane Grafting Of Compact Hyperbranched Polyglycerols
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Antigens Protected Functional Red Blood Cells By The Membrane Grafting Of Compact Hyperbranched Polyglycerols

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Last Updated: Jun 19, 2026

Immunostaining-Based Detection of Dynamic Alterations in Red Blood Cell Proteins
10:07

Immunostaining-Based Detection of Dynamic Alterations in Red Blood Cell Proteins

Published on: March 17, 2023

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
09:12

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry

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Antigens Protected Functional Red Blood Cells By The Membrane Grafting Of Compact Hyperbranched Polyglycerols
11:31

Antigens Protected Functional Red Blood Cells By The Membrane Grafting Of Compact Hyperbranched Polyglycerols

Published on: January 2, 2013

  • Red blood cell surface exhibits changes below an ionic strength of 0.02, indicating potential surface injury.
  • Isoelectric points for red cells, lipid extract, and stroma protein were determined as approximately 1.7, 2.6, and 4.7, respectively.
  • pH-mobility data suggest a lipid-dominated surface with strong acid groups.

Conclusions:

  • The human red blood cell surface is largely composed of lipids.
  • Strong acid groups, potentially from cephalin molecules, dominate the red cell surface charge.
  • Ionic strength significantly influences red blood cell surface behavior and integrity.