Related Experiment Video
Updated: Jun 19, 2026

09:07
Single-cell Screening Method for the Selection and Recovery of Antibodies with Desired Specificities from Enriched Human Memory B Cell Populations
Published on: August 22, 2019
QUANTITATIVE EXPERIMENTS WITH ANTIBODIES TO A SPECIFIC PRECIPITATE. I
1Department of Medicine, College of Physicians and Surgeons, Columbia University, and the Presbyterian Hospital, New York.
The Journal of Experimental Medicine
|October 30, 2009
Summary
Antibody specificity was investigated using quantitative agglutinin methods. Results indicate that antibody function arises from common origins, with specific groupings being either small or non-antigenic.
Area of Science:
- Immunology
- Biochemistry
Background:
- Antibody specificity is crucial for immune responses.
- Understanding the antigenic determinants of antibodies aids in vaccine development and therapeutic strategies.
Purpose of the Study:
- To quantitatively assess the antigenic specificity of antibodies.
- To determine the nature of the antigenic groupings responsible for antibody function.
Main Methods:
- Rabbits were immunized with specific precipitates from various horse antisera.
- Antibody levels in antisera were quantified using quantitative agglutinin assays.
- Specific precipitates and purified antibodies were used to remove homologous antibodies from immune sera.
Main Results:
- Specific precipitates from antipneumococcus, anti-Pn, and anti-influenza horse sera removed equivalent amounts of antibody.
- Purified antibodies behaved similarly to their homologous specific precipitates in antibody removal.
- Specific precipitates from anti-egg albumin and anti-diphtheria sera removed only a fraction of the antibody.
- Pepsin-digested Type I antipneumococcus antibody precipitate removed all homologous antibody but followed a different quantitative course.
Conclusions:
- The primary antigenic specificity of the investigated antibodies is attributed to their common origin.
- The functional antibody groupings are either a small portion of the protein molecule or non-antigenic.

