| Literature DB >> 2526319 |
A G Craig1, D Nizetic, H Lehrach.
Abstract
The normal procedure for labelling oligonucleotides radioactively is the use of polynucleotide kinase and gamma 32P-ATP. However, this has the disadvantage of only introducing one labelled base per molecule of the oligonucleotide. In this paper we describe an approach based on primer/template combinations using conventional fill-in conditions followed by the release of the labelled sequence by digestion with uracil-DNA glycosylase.Entities:
Mesh:
Substances:
Year: 1989 PMID: 2526319 PMCID: PMC318018 DOI: 10.1093/nar/17.12.4605
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971