“…This protocol, which is derived from earlier procedures (Siegelman and Firer, 1964;Hopkins and Butler, 1970) with modifications to minimize proteolysis and accommodate differences in properties between the degraded and undegraded forms of phytochrome, utilizes sequential column chromatography with brushite, diethylaminoethyl-cellulose, hydroxylapatite, Bio-Gel Al.5 M and Sephadex G-200. The product has an apparent molecular weight of about 400,000 daltons based upon calibrated gel exclusion chromatography and is homogeneous by gel electrophoresis (Rice and Briggs, 1973b). The purity of such a homogeneous preparation, expressed as the specific absorbance ratio ( & 6 7 / A 2 8 0 after far red irradiation) is about 0.7 (Table 1).…”