Double antibody methods are applicable to all radioimmunoassay systems. At least three approaches exist. The first, in which immunoprecipitating serum is used to precipitate soluble antigen-antibody complexes, is the most commonly used. Since the effects of interfering factors, especially those present in serum, become minimal as equilibrium is approached, care must be taken to insure that the period of incubation is of sufficient length for the immunoprecipitation reaction to reach equilibrium. In general, all efforts should focus on achieving reaction conditions which maximize stability and optimize immunoprecipitation. A second approach involves use of the first antiserum in an insolubilized form after prior precipitation with the immunoprecipitating antiserum. This approach is attractive since most non specific factors cannot interfere with the immunoprecipitation step to a significant extent once the formation of antigen-antibody aggregates is well underway. The third approach, in which immunoprecipitating antiserum is conjugated to a solid matrix, in principle represents a more ideal method of separating bound hormone from free. If this approach is ever to be utilized, a method of conjugating antiserum to a suitable matrix such that the antibody retains most of its immunoreactivity must be devised.