“…The excitation wavelength was 280 or 290 nm, and the emission maximum was at 338 nm for the rabbit protein (this work) and at 328 nm for human HRG (Morgan, 1978). For absorption, ligand added to equal volumes of buffer served as reference solutions; with fluorescence, ligand added to ovalbumin was used to correct for screening and inner-filter effects (Morgan et al, 1975), except for mercury which quenches ovalbumin fluorescence (Chen, 1976). Spectral measurements were usually made within minutes of mixing protein with ligand, and no changes after this time were noted.…”