“…At the termination of the incubation period, the slices were washed in cold saline, blotted on filter paper, placed in 2 ml of extraction medium in a boiling water bath for 90 sec and homogenized. The extraction media used were 0.25M glycylglycine buffer pH 2.0 for oxidized pyridine nucleotides and 0.25M glycylglycine buffer pH 12.0 for reduced pyridine nucleotides (6).…”