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Related Concept Videos

Cross-reactivity00:42

Cross-reactivity

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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
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Antibody Structure

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Enzyme-Linked Immunosorbent Assay01:33

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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.
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A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

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Published on: March 25, 2014

EpiC: an open resource for exploring epitopes to aid antibody-based experiments.

Niall J Haslam1, Toby J Gibson

  • 1European Molecular Biology Laboratory, Structural and Computational Biology Unit, Heidelberg, Germany. niall@sgenomics.org

Journal of Proteome Research
|May 26, 2010
PubMed
Summary

Antibodies are essential research tools, but experimental needs challenge their capabilities. A new web resource, EpiC, aids in selecting optimal epitopes for antibody production, supporting future proteomic research.

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Area of Science:

  • Proteomics and Antibody Research
  • Bioinformatics and Reagent Development

Background:

  • Antibodies are critical research tools in biology, enabling sensitive protein identification.
  • Diverse experimental requirements strain antibody capabilities, necessitating well-characterized affinity reagents.
  • Growing demand for antibodies, driven by expanding therapeutic targets, highlights the need for improved production tools.

Purpose of the Study:

  • To address the need for better antibody production tools.
  • To introduce a freely available web resource for epitope selection and protein characterization.
  • To support the proteomics community in developing well-characterized affinity reagents.

Main Methods:

  • Development of a freely available web resource, the Epitope Choice Resource (EpiC).
  • Integration of bioinformatic tools for up-to-date data on protein epitopes.
  • Creation of a centralized portal for exploring epitopes on target proteins.

Main Results:

  • EpiC provides a single web portal for epitope exploration.
  • The resource connects to various bioinformatic tools for current data.
  • It facilitates the selection of epitopes for antibody development.

Conclusions:

  • EpiC supports the proteomics community by aiding in the selection of optimal epitopes.
  • The resource is crucial for developing well-characterized antibodies for future research.
  • Accessible tools like EpiC are vital for advancing proteome-scale biology and therapeutic target identification.