Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 30
cDNAs inserted in this way into expression vectors such as lgt20 and agt22 have
only one chance in six of being expressed in bacteria : Only one half of the cDNA
molecules will be inserted into the vector in the correct orientation with respect ...
cDNAs inserted in this way into expression vectors such as lgt20 and agt22 have
only one chance in six of being expressed in bacteria : Only one half of the cDNA
molecules will be inserted into the vector in the correct orientation with respect ...
Page 39
Other Bacteriophage à Vectors Used for cDNA Cloning MORF8 cDNAs inserted
into Igt11 have only one chance in six of being expressed in bacteria : Only one
half of the cDNA molecules will be inserted into the vector in the correct ...
Other Bacteriophage à Vectors Used for cDNA Cloning MORF8 cDNAs inserted
into Igt11 have only one chance in six of being expressed in bacteria : Only one
half of the cDNA molecules will be inserted into the vector in the correct ...
Page 86
Designing the Hexameric Linker Before starting hexameric linker mutagenesis , it
is necessary to decide ( 1 ) which restriction enzyme will be used to linearize the
plasmid DNA and ( 2 ) the restriction site that will be inserted into the target ...
Designing the Hexameric Linker Before starting hexameric linker mutagenesis , it
is necessary to decide ( 1 ) which restriction enzyme will be used to linearize the
plasmid DNA and ( 2 ) the restriction site that will be inserted into the target ...
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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