Microdetermination of dolichol in tissues.

A method is described for the rapid purification and analysis of tissue dolichol on a nanomole scale. The assay is based on a radioisotope dilution technique in which [3H]dolichyl palmitate is used as tracer and acetylation with [14C]acetic anhydride serves as the quantitating reaction. The acetylation conditions were characterized with respect to time, temperature and concentration of reagents. When this method was applied to pig liver, a value was obtained which fell within the range of previously published results based on a gravimetric assay. In chicken, dolichol levels were found to be high in oviduct and low or absent in red blood cells and plasma.