Santagati S, Bettini E, Asdente M, Muramatsu M, Maggi A
Milano Molecular Pharmacology Laboratory, University of Milan, Italy.
Biochem Pharmacol. 1993 Nov 17;46(10):1797-803. doi: 10.1016/0006-2952(93)90585-k.
The necessary theoretical considerations for the development of a correct quantitative analysis of a low abundance messenger RNA (mRNA), estrogen receptor mRNA, by competitive polymerase chain reaction (PCR) are presented together with a series of experimental data. When compared to other methodologies currently utilized for RNA quantitation, this PCR application proved to be a very reliable, rapid and sensitive method. Furthermore, the PCR-based quantitative method described is of particular interest since it does not require the use of radiolabeled compounds.