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Related Concept Videos

Hybridoma Technology01:31

Hybridoma Technology

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Hybridoma technology is used for the large-scale production of monoclonal antibodies. Monoclonal antibodies bind to only a single antigenic determinant or epitope. Such antibodies are used in research, diagnostics, and disease therapy. The hybridoma technology established in 1975 by Georges Köhler and Cesar Milstein was awarded the Nobel Prize in Medicine in 1984 for revolutionizing research and therapy.
Hybridoma Selection
Commonly used fusion techniques — electroporation,...
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Related Experiment Video

Updated: Dec 7, 2025

A Microfluidic Chip for the Versatile Chemical Analysis of Single Cells
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A microfluidic chip for screening high-producing hybridomas at single cell level.

Weikai Zhang1, Ren Li, Fei Jia

  • 1Department of Biomedical Engineering, School of Life Science, Beijing Institute of Technology, Beijing 100081, China. weizewen@bit.edu.cn liqin@bit.edu.cn.

Lab on a Chip
|October 2, 2020
PubMed
Summary

This study introduces a novel microfluidic chip for screening hybridomas, improving monoclonal antibody (mAb) production. The chip streamlines multiple screening steps, enhancing accuracy and reducing costs for hybridoma cell line development.

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Area of Science:

  • Biotechnology
  • Immunology
  • Microfluidics

Background:

  • Hybridomas are essential for monoclonal antibody (mAb) production in research and therapy.
  • Long-term hybridoma cultures lead to population heterogeneity and reduced antibody production.
  • Current screening methods are laborious and inefficient, often performed in multi-well plates.

Purpose of the Study:

  • To develop a novel microfluidic chip for efficient, single-cell level screening of hybridomas.
  • To overcome the limitations of traditional multi-well plate screening methods for hybridoma selection.
  • To improve the accuracy and monoclonality of monoclonal antibody production.

Main Methods:

  • Development of a single microfluidic chip integrating hybridoma trapping, proliferation, and transfer.
  • Incorporation of fluorescent identification for single-cell protein-antibody binding analysis.
  • Two-round screening of anti-CD45 mAb-secreting hybridomas using the microfluidic platform.

Main Results:

  • The microfluidic chip successfully screened high-producing hybridomas with minimal cell loss.
  • Demonstrated significant reduction in human labor and time costs compared to conventional methods.
  • Achieved enhanced accuracy and confirmed monoclonality in the selected hybridoma population.

Conclusions:

  • The novel microfluidic chip offers a comprehensive solution for multi-round hybridoma screening.
  • This technology enhances efficiency, accuracy, and monoclonality in monoclonal antibody production.
  • The platform is suitable for both laboratory studies and pilot-scale production of therapeutic mAbs.