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Titlebook: Epstein-Barr Virus Protocols; Joanna B. Wilson,Gerhard H. W. May Book 2001 Humana Press 2001

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https://doi.org/10.1007/978-1-4757-3500-0NA migrate with known and different mobilities, the Gardella gel (.), and combined it with a highly sensitive DNA polymerase chain reaction (PCR) system (.,., and . in this volume), that can be used to detect a single copy of the viral genome in 10. uninfected cells. The result is a technique that c
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Sociological Aspects of European Integrationociated with a selection process (.,.). This selection process prevents the analysis of early effects of expressed viral genes and could also lead to secondary cell culture effects not associated with the viral gene. Often, inducible gene expression systems are difficult to modulate and can be leaky
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Analysis of Replication of oriP-Based Plasmids by Quantitative, Competitive PCRated DNAs in both short-term and long-term assays (.). Quantitative, competitive PCR can be used to study both the contribution of proteins to the replication of oriP-based plasmids (.) as well as the requirements for specific DNA sequences to support replication of a plasmid (.). Advantages of this
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Construction of cDNA Libraries for the Analysis of the Structure of Complementary Strand Transcriptsm a common promoter that exhibit a complex splicing pattern and contain a number of small open reading frames with the potential to encode a number of proteins (.). The CSTs have been detected in most types of EBV infection, including nasopharyngeal carcinoma (NPC) (.), oral hairy leukoplakia (.), E
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Analysis of the Expression and Function of the EBV-Encoded Small RNAs, the EBERs, in Heterologous Ceir functions in relation to the physiology of the virus remain enigmatic. In recent years, the main interest in the EBERs has been in connection with the use of these RNAs as targets for identification of EBV infection using . hybridization. However evidence for a possible function for the EBERs is
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