Degradable dUMP Outer Primers in Merged Tandem (M/T)-Nested PCR: Low- and Single-Copy DNA Target Amplification
Open Access
- 1 October 1998
- journal article
- Published by Elsevier in Analytical Biochemistry
- Vol. 263 (1) , 85-92
- https://doi.org/10.1006/abio.1998.2771
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Nanoliter scale PCR with TaqMan detectionNucleic Acids Research, 1997
- A Novel PCR Technique UsingAlu-Specific Primers to Identify Unknown Flanking Sequences from the Human GenomeGenomics, 1995
- Assembly and cloning of coding sequences for neurotrophic factors directly from genomic DNA using polymerase chain reaction and uracil DNA glycosylaseGene, 1994
- Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplificationNature Genetics, 1994
- Uracil DNA glycosylase-mediated cloning of polymerasechain reaction-amplified DNA: Application to genomic and cDNA cloningAnalytical Biochemistry, 1992
- Use of modified nucleotides and uracil-DNA glycosylase (UNG) for the control of contamination in the PCR-based amplification of RNAMolecular and Cellular Probes, 1992
- The use of uracil-N-glycosylase in the preparation of PCR products of direct sequencingNucleic Acids Research, 1992
- Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase.Genome Research, 1991
- Enhanced detection by PCR of hepatitis C virus RNAThe Lancet, 1990
- Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactionsGene, 1990