Protein contaminated with nucleic acids absorbed the light at wavelength 280 nm and it absorbs much strongly at wavelength 205 nm when it is free from nucleic acids. The UV-visible spectrophotometer was used in determination of saliva proteins (Figure 2.2). Cold trichloroacetic acid (10 % w/v ) was added to the sample, centrifuged for 10 minutes to precipitate protein. The absorbance of a known volume ( 50 µl) of sample diluted with 4 milliliters distil water was measured at wavelengths 205 nm , 260 and 280 nm for each subject and patient . The concentrations of contaminated and uncontaminated proteins were determined by using the following equations (Layne, 1957; Scopes, 1974; Stoscheck, 1990):
Protein contaminated with nucleic acids absorbed the light at wavelength 280 nm and it absorbs much strongly at wavelength 205 nm when it is free from nucleic acids. The UV-visible spectrophotometer was used in determination of saliva proteins (Figure 2.2). Cold trichloroacetic acid (10 % w/v ) was added to the sample, centrifuged for 10 minutes to precipitate protein. The absorbance of a known volume ( 50 µl) of sample diluted with 4 milliliters distil water was measured at wavelengths 205 nm , 260 and 280 nm for each subject and patient . The concentrations of contaminated and uncontaminated proteins were determined by using the following equations (Layne, 1957; Scopes, 1974; Stoscheck, 1990):