»Anti-B Blood Grouping Serum conforms to the regulations of the federal Food and Drug Administration concerning biologics (660.20to 660.29)(see
Biologics á1041ñ).It is a sterile,liquid or dried preparation containing the particular blood group antibodies derived from high-titered blood plasma or serum of human subjects,with or without stimulation by the injection of Blood Group Specific Substance B(or AB).It agglutinates human red cells containing B-antigens,i.e.,blood groups Band AB(including subgroups A
1Band A
2B).It contains a suitable antimicrobial preservative.It meets the requirements of the test for potency,in parallel with,and not less than equivalent to,the U.S.Reference Blood Grouping Serum Anti-B,in agglutinating red blood cells from Group Bdonors.It meets the requirements of the tests for specificity with Group A
1,B,and Ocells and confirms the absence of contaminating antibodies reactive with M
g,Wr
aantigens as well as other antigens having an incidence of 1percent or greater in the general population (see under
Blood Grouping Serums Anti-D,
Anti-C,
Anti-E,
Anti-c,
Anti-e).It meets the requirements of the test for avidity with Group Bcells.All fresh or frozen red blood cell suspensions used for these tests are prepared under specified conditions and meet specified criteria.Anti-B Blood Grouping Serum may be artificially colored yellow.