Quantitation of targets for PCR by and use of limiting dilution

Pam Sykes, S. H. Neoh, M. J. Brisco, E. Hughes, J. Condon, A. A. Morley

Research output: Chapter in Book/Report/Conference proceedingChapter


We describe a general method to quantitate the total number of initial targets present in a sample using limiting dilution, PCR and Poisson statistics. The DNA target for the PCR was the rearranged immunoglobulin heavy chain (IgH) gene derived from a leukemic clone that was quantitated against a background of excess rearranged IgH genes from normal lymphocytes. The PCR was optimized to provide an all-or-none end point at very low DNA target numbers. PCR amplification of the Nras gene was used as an internal control to quantitate the number of potentially amplifiable genomes present in a sample and hence to measure the extent of DNA degradation. A two-stage PCR was necessary owing to competition between leukemic and non-leukemic templates. Study of eight leukemic samples showed that approximately two potentially amplifiable leukemic IgH targets could be detected in the presence of160000 competing non-leukemic genomes. The method presented quantitates the total number of initial DNA targets present in a sample, unlike most other quantitation methods that quantitate PCR products. It has wide application, because it is technically simple, does not require radioactivity, addresses the problem of excess competing targets and estimates the extent of DNA degradation in a sample.
Original languageEnglish
Title of host publicationThe PCR Technique
Subtitle of host publicationQuantitative PCR
EditorsJames W. Larrick
Place of PublicationMassachusetts, U.S.A.
Number of pages13
ISBN (Print)9781881299066, 1-881299-06-6
Publication statusPublished - 1997
Externally publishedYes

Publication series

NameBiotechniques Update Series
PublisherEaton Publishing Co.


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