Abstract
Summary
Bacterial agglutinins were removed partly by intact bacteria or cell walls from brucella antisera and by absorption with heterologous antigens monospecific antisera were produced. Cell wall agglutination parallels almost completely the agglutination of intact bacteria, when cell wall suspensions of high density were employed. Precipitins for soluble bacterial antigens demonstrable by agar gel precipitation technic were nonspecific and were removed by relatively small amounts of absorbing antigens.
Get full access to this article
View all access options for this article.