Internal Control DNA for PCR Assays Introduced into Lambda Phage Particles Exhibits Nuclease Resistance
Authors:
Open Access
- 1 November 2004
- journal article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 50 (11) , 2163-2166
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Practical Considerations in Design of Internal Amplification Controls for Diagnostic PCR AssaysJournal of Clinical Microbiology, 2004
- Automated detection of five human herpes virus DNAs by a set of LightCycler PCRs complemented with a single multiple internal controlJournal of Clinical Virology, 2004
- Fully Automated, Internally Controlled Quantification of Hepatitis B Virus DNA by Real-Time PCR by Use of the MagNA Pure LC and LightCycler InstrumentsJournal of Clinical Microbiology, 2004
- A convenient approach to the generation of multiple internal control DNA for a panel of real-time PCR assaysJournal of Virological Methods, 2003
- Diagnosing Herpesvirus Infections by Real-Time Amplification and Rapid CultureJournal of Clinical Microbiology, 2003
- Real-time PCR in virologyNucleic Acids Research, 2002
- Detection of Legionellae in Hospital Water Samples by Quantitative Real-Time LightCycler PCRApplied and Environmental Microbiology, 2001
- Purification and Characterization of PCR-Inhibitory Components in Blood CellsJournal of Clinical Microbiology, 2001
- Armored RNA Technology for Production of Ribonuclease-Resistant Viral RNA Controls and StandardsJournal of Clinical Microbiology, 1998
- [40] Cloning cDNA into λgt10 and λgt111987