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Related Concept Videos

Southern Blot02:57

Southern Blot

Agarose gel electrophoresis is very useful in separating DNA fragments by size. Running a DNA ladder containing fragments of the known length alongside the sample helps determine the approximate length of the sample DNA fragments. However, additional steps are needed to verify the sequence identity of the sample DNA fragments.
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
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...
Western Blotting01:15

Western Blotting

Western blotting is an analytical technique for protein identification. It has various applications in immunology and medicine, including detecting diseases like bovine spongiform encephalopathy, mad cow disease, and human and feline immunodeficiency virus from biological samples.
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.
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.
Immunocytochemistry and Immunohistochemistry01:22

Immunocytochemistry and Immunohistochemistry

Immunocytochemistry (ICC) and immunohistochemistry (IHC) are techniques that use antibodies to check for specific proteins or antigens in a sample. The technique was first published by Albert Coons in 1941 to detect the presence of pneumococcal antigen in tissue sections from mice infected with Pneumococcus. Immunocytochemistry helps localization of proteins or antigens in individual cells like blood cells, stem cells, etc., while immunohistochemistry does the same for tissue samples.
These...

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Related Experiment Video

Updated: May 26, 2026

Immunoblot Analysis
16:01

Immunoblot Analysis

Published on: June 20, 2008

[An immunoblot technique]

T Imai1

  • 1Faculty of Science, Toho University.

Nihon Rinsho. Japanese Journal of Clinical Medicine
|September 1, 1995
PubMed
Summary
This summary is machine-generated.

The immunoblot technique uses gel electrophoresis and immunological detection to analyze proteins with high specificity and sensitivity. This method is crucial for understanding human protein physiopathology in various scientific fields.

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Last Updated: May 26, 2026

Immunoblot Analysis
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Area of Science:

  • Biochemistry and Molecular Biology
  • Human Genetics
  • Immunology

Context:

  • Protein analysis is essential in medicine, biochemistry, molecular biology, and human genetics.
  • The immunoblot technique integrates gel electrophoresis for separation with immunological detection for specificity.
  • This method is widely adopted for its high sensitivity and specificity in protein analysis.

Purpose:

  • To efficiently transfer target proteins from a gel matrix to a membrane.
  • To enable unique and sensitive immunological detection of specific proteins.
  • To provide a versatile platform for analyzing diverse protein targets.

Summary:

  • The immunoblot technique involves separating proteins via gel electrophoresis and transferring them to a membrane for detection.
  • Key components for successful immunoblotting include the transfer system, membrane type, buffer composition, optimal conditions, and detection reagents.
  • The method relies on specific antibodies for precise identification of target proteins.

Impact:

  • Facilitates the determination of human protein physiopathology.
  • Enables broad applications in medical diagnostics and biological research.
  • Advances the understanding of diseases at a molecular level through protein analysis.