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. |
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Page 11
... concentration of 0.8 mM ; this leaves 0.7 mM of the original 1.5 mM MgCl2 not complexed with dNTP . Consequently , if the dNTP concentration is changed significantly , a compensatory change in MgCl , may be necessary . Taq polymerase is ...
... concentration of 0.8 mM ; this leaves 0.7 mM of the original 1.5 mM MgCl2 not complexed with dNTP . Consequently , if the dNTP concentration is changed significantly , a compensatory change in MgCl , may be necessary . Taq polymerase is ...
Page 18
... concentration that is required to maximally activate the enzyme is dependent on the dNTP concentration . In addition , at the correspondingly optimal magnesium concentration , the synthesis rate of Taq polymerase decreases by as much as ...
... concentration that is required to maximally activate the enzyme is dependent on the dNTP concentration . In addition , at the correspondingly optimal magnesium concentration , the synthesis rate of Taq polymerase decreases by as much as ...
Page 93
... concentration to 0.2 mM , a concentration that is more optimal for the Taq polymerase . The dNTP concentration should not exceed 0.2 mM because higher concentrations have been found to result in a higher misincorporation rate or ...
... concentration to 0.2 mM , a concentration that is more optimal for the Taq polymerase . The dNTP concentration should not exceed 0.2 mM because higher concentrations have been found to result in a higher misincorporation rate or ...
Contents
PART ONE BASIC METHODOLOGY | 1 |
PCR Amplification of Specific Sequences from | 9 |
Taq DNA Polymerase | 17 |
Copyright | |
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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 B-globin cDNA cells Cetus chromosome cloned concentration containing cycles deletion denaturant denaturing gradient gel detection DGGE diagnosis direct sequencing disease DNA fragments DNA sequences dNTP dot-blot dystrophin Erlich exon Faloona Figure flanking GC-clamp Gelfand gene 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 sequence temperature template Tris.HCl tube