Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 3-4
... Package in vitro into bacteriophage X particles Infect E. coli and select for amp'
transformants Ampr colonies carrying recombinant cosmids FIGVMtE 3.1 The
figure shows in diagrammatic form the steps involved in cloning in cosmid vectors
.
... Package in vitro into bacteriophage X particles Infect E. coli and select for amp'
transformants Ampr colonies carrying recombinant cosmids FIGVMtE 3.1 The
figure shows in diagrammatic form the steps involved in cloning in cosmid vectors
.
Page 3-5
Cloning in Cosmid Vectors In their simplest form , cosmid vectors are modified
plasmids that carry a copy of the DNA sequences ( cos sequences ) required for
packaging DNA into bacteriophage à particles . Because cosmids carry an origin
of ...
Cloning in Cosmid Vectors In their simplest form , cosmid vectors are modified
plasmids that carry a copy of the DNA sequences ( cos sequences ) required for
packaging DNA into bacteriophage à particles . Because cosmids carry an origin
of ...
Page 3-52
Preparation of a Transducing Lysate of Packaged Cosmids Because circular
cosmid molecules carried in bacterial cells contain a cos site , they can be
efficiently packaged into bacteriophage à particles . When cosmid - containing
bacteria are ...
Preparation of a Transducing Lysate of Packaged Cosmids Because circular
cosmid molecules carried in bacterial cells contain a cos site , they can be
efficiently packaged into bacteriophage à particles . When cosmid - containing
bacteria are ...
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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