“…(b) Immunocytochemial staining was conducted as described previously [4], The slides were exposed to a dilute solution of a specific rabbit antiserum against human-factor-VIlI-related antigen (Hoechst Canada Inc., Montreal, Que., Canada), incubated for 2h at room temperature, washed in Tris buffer and then reincubated with a dilute solution of peroxidase- conjugated goat antirabbit globulins (Hoechst). After repeated washing, the final exposure was to a solution of 0.05% diaminobenzidine hydrochloride (Sigma) and 0.01 % hydrogen peroxide (Anachemia Chemicals Ltd., Montreal, Que., Canada) in 0.05 M Tris buffer at pH 7.6 for 10 min.…”