Abstract
By means of separating antisera into fractions with different rates of association, it has been demonstrated that rabbit anti-BSA is heterogeneous with respect to its rate of combination with antigen. This separation was accomplished by: a) fractionation according to total molecular charge; b) rapid, partial absorption with a particulate BSA preparation; c) partial in vivo clearance of anti-BSA with antigen. It was possible to select antibody molecules on the basis of their combination rate without a significant alteration in the dissociation rate, thereby indicating that these two processes are, at least in part, independent of each other.