Summary
A two-stage method employing purified clotting factors for the assay of tissue-TPLN
is described in detail. The rate of prothrombin activation is determined in the presence
of optimum amounts of factors V, VII, X and Ca++. The activation of prothrombin is arrested by addition of EDTA or STI, and the thrombin
formed is assayed by the clotting method. The method is rapid, sensitive, reproducible
and can differentiate between the tissue-TPLN activity of intact lipo-protein and
the procoagulant activity of the phospholipids.