Overview
- Editors:
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Leda Raptis
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Queen’s University, Kingston, Canada
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Table of contents (20 protocols)
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- James D. Tremblay, Kris F. Sachsenmeier, James M. Pipas
Pages 1-7
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- Christine K. Liu, Walter J. Atwood
Pages 9-17
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- Kodangattil R. Sreekumar, Brett A. Barbaro, Andrea E. Prack, Peter A. Bullock
Pages 49-67
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- Richard J. Kraus, Janet E. Mertz
Pages 69-85
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- Richard J. Kraus, Janet E. Mertz
Pages 87-101
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- David S. Strayer, Maria Lamothe, Danlan Wei, Joseph Milano, Rumi Kondo
Pages 103-117
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- Ziv Sandalon, Ariella Oppenheim
Pages 119-128
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- Van Cherington, Cynthia Higgins
Pages 129-150
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- Leda Raptis, Adina Vultur
Pages 151-164
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- Cynthia Higgins, Van Cherington
Pages 165-183
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- Mary Judith Tevethia, Harvey L. Ozer
Pages 185-199
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- Juan Zalvide, James A. DeCaprio, Hilde Stubdal
Pages 213-218
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- Heather L. Brownell, Leda Raptis
Pages 219-228
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- Ximena Montano, Kathy Rundell
Pages 229-242
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- Todd D. Schell, Satvir S. Tevethia
Pages 243-256
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- John A. Lednicky, Robert L. Garcea
Pages 257-267
About this book
Simian virus 40 gained notoriety in the 1960s because it was found to be a contaminant of polio and adenovirus vaccines that had been administered to millions of healthy individuals worldwide. The public health implications of this revelation provided the initial impetus for an in-depth study of SV40 biology. Later work showed that SV40 DNA sequences as well as infectious virus are in fact found in human tumors and may have contributed to oncog- esis. It also turned out that SV40 uses mostly cellular machinery to carry out many steps in viral infection, which makes it a powerful probe for examining many fundamental questions in eukaryotic molecular biology. SV40 Pro- cols consolidates a number of well-tested step-by-step techniques in one v- ume; experts with hands-on experience in particular methods give detailed accounts of their optimized experimental protocols, so that the beginner, as well as more experienced researchers, may readily overcome problems of ambiguity often present in the literature. As with other DNA tumor viruses, the response of cultured cells to SV40 infection depends upon the species being infected. Monkey cells s- port virus production, which leads to their death, whereas rodent cells p- duce only the early proteins and acquire a transformed phenotype. Thus, SV40 Protocols is organized in two sections. The first relates to assays of the lytic cycle of the virus, and the second deals with transformation.
Editors and Affiliations
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Queen’s University, Kingston, Canada
Leda Raptis