PCR Technology: Principles and Applications for DNA AmplificationThis is an introduction to the methods and applications of polymerase chain reaction (PCR) technology, a technology developed by Erlich's group at Cetus and Cetus, and is expected to be used in all biology laboratories worldwide within the next few years. |
From inside the book
Results 1-5 of 87
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... Sequence Primers for Amplification of Human DNA from Complex Sources 113 David L. Nelson and C. Thomas Caskey A New Approach to Constructing Genetic Maps : PCR Analysis of DNA Sequences in Individual Gametes 119 Norman Arnheim 13 ...
... Sequence Primers for Amplification of Human DNA from Complex Sources 113 David L. Nelson and C. Thomas Caskey A New Approach to Constructing Genetic Maps : PCR Analysis of DNA Sequences in Individual Gametes 119 Norman Arnheim 13 ...
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Principles and Applications for DNA Amplification Henry Erlich. human B - globin DNA and to the prenatal diagnosis of ... sequence in the genomic template . " This effect was revealed by experiments in which normal genomic DNA ( with two ...
Principles and Applications for DNA Amplification Henry Erlich. human B - globin DNA and to the prenatal diagnosis of ... sequence in the genomic template . " This effect was revealed by experiments in which normal genomic DNA ( with two ...
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Principles and Applications for DNA Amplification Henry Erlich. The use of ... sequence , it is also a very powerful and precise way of altering a ... nucleotide substitutions , insertions , and deletions can also be introduced into the ...
Principles and Applications for DNA Amplification Henry Erlich. The use of ... sequence , it is also a very powerful and precise way of altering a ... nucleotide substitutions , insertions , and deletions can also be introduced into the ...
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... sequence analysis of individual clones derived from a PCR , sequences must be determined from multiple clones to distinguish misincorporated nucleotides from the faithful copes of the template sequence . Other DNA ... DNA polymerase , can ...
... sequence analysis of individual clones derived from a PCR , sequences must be determined from multiple clones to distinguish misincorporated nucleotides from the faithful copes of the template sequence . Other DNA ... DNA polymerase , can ...
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... DNA fragment from small amounts of a complex template . Recombinant DNA techniques create molecular clones by conferring on a specific sequence the ability to replicate by inserting it into a vector and introducing the vector into a ...
... DNA fragment from small amounts of a complex template . Recombinant DNA techniques create molecular clones by conferring on a specific sequence the ability to replicate by inserting it into a vector and introducing the vector into a ...
Contents
1 | |
9 | |
17 | |
PCR Automation | 23 |
Simple and Rapid Preparation | 31 |
PART TWO RESEARCH APPLICATIONS | 39 |
Using PCR to Engineer DNA | 61 |
Mutation Detection by PCR GCClamps | 71 |
The Use of Repeat Sequence | 113 |
A New Approach to Constructing Genetic | 119 |
Evolutionary Analysis via PCR | 137 |
PART THREE MEDICAL APPLICATIONS | 149 |
Diagnosis of New Mutation Diseases Using | 171 |
Applications of PCR to the Analysis | 209 |
Detection of ras Oncogenes Using PCR | 225 |
Application of PCR to the Detection | 235 |
Other editions - View all
PCR Technology: Principles and Applications for DNA Amplification Henry Erlich No preview available - 1989 |
Common terms and phrases
Acad Acids Res agarose alleles amplification amplification products amplified DNA analysis annealing assay automated cDNA cells Cetus chromosome cloned concentration containing cycles deletion denaturant denaturing gradient gel detection DGGE diagnosis direct sequencing DNA fragments DNA sequences dNTP dot-blot dystrophin Erlich exon Faloona Figure flanking GC-clamp gel electrophoresis Gelfand genetic genomic genomic DNA heteroduplexes Higuchi HPRT human hybridization incubation inverse PCR lane Lerman loci locus markers melting behavior melting domain method misincorporation mismatch molecular molecules mRNA Mullis mutations Natl Nucl nucleotide oligonucleotide primers PCR amplification PCR buffer PCR fragments PCR primers PCR product PCR reaction pmol polymerase chain reaction polymorphism primers Proc procedure protein Proteinase Proteinase K Protocol recombination region restriction enzyme reverse transcriptase Saiki Scharf sequencing reactions single-stranded specific ssDNA strands synthesis Taq DNA polymerase Taq polymerase target DNA target sequence temperature template Tris.HCl tube