Molecular Cloning: A Laboratory Manual, Book 2 |
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Page xxvii
68 Cloning by Expression of cDNA Clones 16 . 69 Expression Cloning of
Genomic DNA 16 . 70 References 16 . 73 17 Expression of Cloned Genes in
Escherichia coli Production of Fusion Proteins 17 . 3 Vector Systems for the
Expression of ...
68 Cloning by Expression of cDNA Clones 16 . 69 Expression Cloning of
Genomic DNA 16 . 70 References 16 . 73 17 Expression of Cloned Genes in
Escherichia coli Production of Fusion Proteins 17 . 3 Vector Systems for the
Expression of ...
Page 6
Genomic DNA and cDNA Expression Libraries Two types of expression libraries
can be constructed in plasmid and bacteriophage i expression vectors : cDNA
and genomic DNA libraries . For prokaryotic organisms , whose genomes contain
...
Genomic DNA and cDNA Expression Libraries Two types of expression libraries
can be constructed in plasmid and bacteriophage i expression vectors : cDNA
and genomic DNA libraries . For prokaryotic organisms , whose genomes contain
...
Page 8
Expression Libraries Constructed in Plasmids Most cDNA expression libraries
constructed in plasmid expression vectors use ... reading frames , any open
reading frame of a sequenced fragment of DNA can be easily cloned for
expression .
Expression Libraries Constructed in Plasmids Most cDNA expression libraries
constructed in plasmid expression vectors use ... reading frames , any open
reading frame of a sequenced fragment of DNA can be easily cloned for
expression .
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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 |
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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