Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 95
Page 2-55
CHOOSING A BACTERIAL HOST FOR BACTERIOPHAGE 1 VECTORS When
using specialized vectors such as bacteriophage 1gtil , it is necessary to use
particular strains of E. coli that have been designed to serve as specific hosts .
CHOOSING A BACTERIAL HOST FOR BACTERIOPHAGE 1 VECTORS When
using specialized vectors such as bacteriophage 1gtil , it is necessary to use
particular strains of E. coli that have been designed to serve as specific hosts .
Page 4-13
The guidelines are no longer in force , but the marker lingers on in several of the
bacterial strains dating from that era . ... but not modification , by the type I
restriction / modification system of E. coli strain K ( for review , see Yuan 1981 ) .
The guidelines are no longer in force , but the marker lingers on in several of the
bacterial strains dating from that era . ... but not modification , by the type I
restriction / modification system of E. coli strain K ( for review , see Yuan 1981 ) .
Page 5-15
DNA METHYLATION Methylation by Commonly Used Strains of E. coli Most
strains of E. coli contain two enzymes that methylate DNA — the dam methylase
and the dcm methylase . dam METHYLASE This enzyme introduces methyl
groups at ...
DNA METHYLATION Methylation by Commonly Used Strains of E. coli Most
strains of E. coli contain two enzymes that methylate DNA — the dam methylase
and the dcm methylase . dam METHYLASE This enzyme introduces methyl
groups at ...
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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
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Common terms and phrases
activity agar agarose aliquots allow amount appropriate arms bacterial bacteriophage BamHI buffer carrying cells centrifugation Chapter cloning coli colonies completely concentration construction containing cosmid culture described digestion EcoRI efficiency electrophoresis et al ethanol ethidium ethidium bromide extracts Figure filters final foreign DNA fragments gene genetic genome growth Hindi host hybridization Incubate infected inserted libraries ligase ligation linear method microfuge minutes minutes at 4°C mixture molecules mutations nucleic acids obtained original packaging particles pellet plaques plasmid DNA plate polycloning polymerase possible precipitate prepared presence probes problem procedure promoter protein purified reaction recombinant Recover region remove replication restriction enzyme room temperature Sall segment selection sequences single single-stranded Smal solution step sterile stored strains strand supernatant termini transfer transformation tube usually vector volume Xbal yield