Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 5
APPLICATIONS OF PCR AMPLIFICATION Although a relatively new technique ,
PCR amplification has already found extensive application in the diagnosis of
genetic disorders ( Wong et al . 1987 ; Engelke et al . 1988 ) , the detection of ...
APPLICATIONS OF PCR AMPLIFICATION Although a relatively new technique ,
PCR amplification has already found extensive application in the diagnosis of
genetic disorders ( Wong et al . 1987 ; Engelke et al . 1988 ) , the detection of ...
Page 10
At the end of the reaction , the amplified DNA is desalted and excess dNTPs are
removed by centrifuge - driven spin dialysis on ... Although this method can work
well , the presence of oligonucleotide primers ( remaining from the amplification ...
At the end of the reaction , the amplified DNA is desalted and excess dNTPs are
removed by centrifuge - driven spin dialysis on ... Although this method can work
well , the presence of oligonucleotide primers ( remaining from the amplification ...
Page 28
Protocol II : Sequencing Single - stranded DNA Templates Generated by
Asymmetric Amplification In this method ( Gyllensten and Erlich 1988 ;
Mihovilovic and Lee 1989 ) , amplification reactions are set up that contain vastly
different molar ...
Protocol II : Sequencing Single - stranded DNA Templates Generated by
Asymmetric Amplification In this method ( Gyllensten and Erlich 1988 ;
Mihovilovic and Lee 1989 ) , amplification reactions are set up that contain vastly
different molar ...
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User Review - iayork - LibraryThingthe BIBLE of every biologist: So few and so much to say about this bible of Biology at the bench... You'll really find everything you want in it, including the composition of all the buffers and ... Read full review
Contents
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
Copyright | |
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Common terms and phrases
acid activity agarose aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies concentration constructed containing deletions denatured described determine digestion DNA polymerase dNTPs double-stranded efficiency electrophoresis et al ethanol expression Figure filters fragment gene genomic hybridization increase Incubate inserted interest isolated labeled length libraries ligation linear linkers method microfuge minutes mixture molecules mRNA mutagenesis mutagenic mutations Nucleic nucleotides obtained oligonucleotide original plaques plasmid plasmid DNA plate pool position possible prepared presence primer probe problem protein purified radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening sequence single single-stranded solution specific step Store strand synthesis target DNA target sequence template termini tion transfer transformants tube units usually vector volume