Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
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Page 2-9
Bacteriophage à Vectors CONSTRUCTION OF BACTERIOPHAGE I VECTORS :
A BRIEF HISTORY At first glance , it would seem a bleak prospect to use
bacteriophage 1 , with its large and complex genome , as a vector . Its DNA
contains ...
Bacteriophage à Vectors CONSTRUCTION OF BACTERIOPHAGE I VECTORS :
A BRIEF HISTORY At first glance , it would seem a bleak prospect to use
bacteriophage 1 , with its large and complex genome , as a vector . Its DNA
contains ...
Page 2-11
Only about 60 % of the viral genome ( the left arm , ~ 20 kb in length , including
the head and tail genes A - J , and the right arm , 8–10 kb in length , from PR
through the cosR site ) is necessary for lytic growth of the bacteriophage ; the
central ...
Only about 60 % of the viral genome ( the left arm , ~ 20 kb in length , including
the head and tail genes A - J , and the right arm , 8–10 kb in length , from PR
through the cosR site ) is necessary for lytic growth of the bacteriophage ; the
central ...
Page 4-3
The Biology of Filamentous Bacteriophages M13 , fi , and fd are very closely
related : Their genomes are organized identically ... More than 98 % of their
nucleotide sequences are identical ; the few differences are scattered around the
genome ...
The Biology of Filamentous Bacteriophages M13 , fi , and fd are very closely
related : Their genomes are organized identically ... More than 98 % of their
nucleotide sequences are identical ; the few differences are scattered around the
genome ...
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LibraryThing Review
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