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 1-3 of 21
Page 2
... discussed in Chapter 1. Although , for any given pair of oligonucleotide primers , an optimal set of conditions can be established , there is no single set of conditions that will be optimal for all possible reactions . ++ The ...
... discussed in Chapter 1. Although , for any given pair of oligonucleotide primers , an optimal set of conditions can be established , there is no single set of conditions that will be optimal for all possible reactions . ++ The ...
Page 39
... discussed in Chapter 5 , the nucleotide sequence of amplified DNA fragments can be determined directly without molecular cloning and preparation of template by growth of the host and biochemical purification of the vector . The study of ...
... discussed in Chapter 5 , the nucleotide sequence of amplified DNA fragments can be determined directly without molecular cloning and preparation of template by growth of the host and biochemical purification of the vector . The study of ...
Page 41
... discussed in Chapter 9 , has been used to amplify cDNA sequences . 20 If the amino acid sequence is an evolutionarily conserved motif in a particular protein ( e.g. , the reverse transcriptase of retroviruses ) , such degenerate primer ...
... discussed in Chapter 9 , has been used to amplify cDNA sequences . 20 If the amino acid sequence is an evolutionarily conserved motif in a particular protein ( e.g. , the reverse transcriptase of retroviruses ) , such degenerate primer ...
Contents
PART ONE BASIC METHODOLOGY | 1 |
The Design and Optimization of the PCR | 7 |
PCR Amplification of Specific Sequences from | 9 |
Copyright | |
17 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 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 disease DNA fragments DNA sequence dNTP dot-blot dystrophin Erlich exon Faloona Figure flanking GC-clamp Gelfand genetic genomic genomic DNA heteroduplexes Higuchi HPRT human hybridization incubation individual 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