PCR Technology: Principles and Applications for DNA AmplificationPolymerase chain reaction (PCR) technology is a revolutionary innovation which enables scientists to rapidly generate large amounts of genetic material from a slight trace which would otherwise be too small to analyze. With applications in both research and diagnostics, PCR is becoming a standard procedure in biotechnology and medical diagnostic laboratories. This book is an introduction and guide to the new technology, covering the basic methodologies and their applications in research and medicine, emphasizing practical aspects. Each chapter is written by pioneers in the field and most include detailed protocols and favorite PCR "recipes". Students and researchers in all areas of biotechnology and molecular biology will find this book the introduction to PCR they've been looking for. |
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Page 18
As observed for several DNA polymerase activities isolated from thermophilic
microorganisms , 94 kDa Taq DNA Polymerase has a relatively high temperature
optimum ( Too for DNA synthesis . Depending on the nature of the DNA template
...
As observed for several DNA polymerase activities isolated from thermophilic
microorganisms , 94 kDa Taq DNA Polymerase has a relatively high temperature
optimum ( Too for DNA synthesis . Depending on the nature of the DNA template
...
Page 19
It is likely that very low dNTP concentrations may adversely affect the processivity
of Tag DNA polymerase . Furthermore , the precise concentration of free and
enzyme - bound magnesium may affect the processivity of Taq polymerase as
has ...
It is likely that very low dNTP concentrations may adversely affect the processivity
of Tag DNA polymerase . Furthermore , the precise concentration of free and
enzyme - bound magnesium may affect the processivity of Taq polymerase as
has ...
Page 53
Sequencing with Thermolabile DNA Polymerases 53 compensated for by
increasing the number of PCR cycles . ... 5 pmol : 50 pmol up to 5 pmol : 50 pmol
, b ) run 5 - 10 more PCR cycles , c ) add more ( 2 units ) Taq polymerase during
the ...
Sequencing with Thermolabile DNA Polymerases 53 compensated for by
increasing the number of PCR cycles . ... 5 pmol : 50 pmol up to 5 pmol : 50 pmol
, b ) run 5 - 10 more PCR cycles , c ) add more ( 2 units ) Taq polymerase during
the ...
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Contents
PART ONE BASIC METHODOLOGY | 1 |
The Design and Optimization of the PCR | 7 |
Taq DNA Polymerase | 17 |
Copyright | |
14 other sections not shown
Other editions - View all
PCR Technology: Principles and Applications for DNA Amplification Henry Erlich No preview available - 1989 |
Common terms and phrases
Acad Acids activity addition alleles allow Alu repeats amount amplification analysis annealing applications approach assay base blood buffer carried cDNA cell changes Chapter clones concentration containing cycles deletion denaturation described detection determined diagnosis digestion direct discussed disease DNA fragments DNA polymerase DNA sequence dNTP domain effect efficient electrophoresis enzyme Erlich example exon extension Figure gene genetic genomic human hybridization identified increase individual initial isolation known lane limited loci locus markers melting method molecular Mullis mutations Nature observed obtained oligonucleotide PCR product performed polymorphic positive possible preparation present primers probes problem Proc procedure Protocol reaction recombination region restriction Saiki samples Science separate shown single specific sperm step strand studies Taq polymerase techniques temperature template tube usually yield
References to this book
Bibliographic information
| Title | PCR Technology: Principles and Applications for DNA Amplification Breakthroughs in Molecular Biology Series |
| Author | Henry A. Erlich |
| Editor | Henry A. Erlich |
| Edition | illustrated, reprint |
| Publisher | Oxford University Press, 1992 |
| Original from | the University of Michigan |
| Digitized | 28 Jul 2008 |
| ISBN | 0195098757, 9780195098754 |
| Length | 246 pages |
| Subjects | › › Literary Criticism / European / English, Irish, Scottish, Welsh |
| Export Citation | BiBTeX EndNote RefMan |