| Literature DB >> 10430034 |
M Maggiolini1, O Donzé, D Picard.
Abstract
We present a novel method for quantitative RT-PCR that involves direct incorporation of digoxigenin-11-dUTP (DIG-dUTP) during amplification of cDNAs, separation of RT-PCR products by agarose gel electrophoresis, Southern transfer to a nylon membrane, and chemiluminescent detection with an anti-DIG antibody. The whole procedure can be done in about a day and has the following advantages: It is highly sensitive, specificity is confirmed by monitoring the size of the RT-PCR product, it is non-radioactive, quantitative, and does not require expensive specialized equipment.Entities:
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Year: 1999 PMID: 10430034 DOI: 10.1515/BC.1999.086
Source DB: PubMed Journal: Biol Chem ISSN: 1431-6730 Impact factor: 3.915