PCR Quantification and Technical Aspects: Multiple Competitors for Single-Tube Quantification of HIV1 DNA; T. Vener, et al. Quantitation of p53 Tumor Suppressor Gene Copy Number in Tumor DNA Samples by Competitive PCR in an ELISA-Format; M. Hahn, et al. Standardisation of Messenger RNA Quantification Using an RTPCR Method Involving Coamplification with a Multi-Specific Internal Control; D. Shire, et al. Quantitative Analysis of Human DNA Sequences by Solid-Phase Minisequencing; A.C. Syvänen. Bioimage Analysers: Application for Ribozyme Kinetics; C.S. Vörtler, K. Birikh. First Approaches to Quantitate MDR1Messenger RNA by in cell PCR; D. Lassner, et al. Application of in situ-PCR for Detection of Intracellular mRNAs; V. Uhlmann, et al. Psoralen Biotin: A Novel Reagent for Non-Enzymatic and Specific Labeling of Nucleic Acid Probes and Oligonucleotides; R.L. Burghoff, et al. The Effect of Quantitative Ratio between Primer Pairs on PCR Products in Multi-Target Amplification; D. Bercovich, et al. PCR Quantification of Infectious Agents: Quantitation of Rubella Virus Genome by QPCR and Its Application to Resolution for Mechanism of Congenital Rubella Syndrome; S. Katow, S. Arai. Significance of the Detection of Rubella Virus RNA by Nested PCR in Prenatal Diagnostics of Viral Infections; B. Pustowoit. Quantitative Detection of Human Cytomegalovirus DNA in Cerebrospinal Fluid by Polymerase Chain Reaction; J.U. Vogel, B. Weber. Quality Control and External Quality Assessment Schemes for the Diagnostic Use of PCR in Microbiological Laboratories-European Trials on Hepatitis B Virus and Cytomegalovirus; J. Schirm. Suppliers of Specialist Items. Index.
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The polymerase chain reaction (PCR) method of nucleic acid replication and modification now rivals traditional cloning, sequencing, and gene detecting procedures. Thirteen papers from the September 1996 meeting provide practical accounts of the authors' particular areas of PCR technology, and discus
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