Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 166
In summary , ligation reactions involving linearized phosphorylated plasmid DNA
with cohesive termini should contain : • Sufficient vector DNA to achieve a j : i
ratio of > 1 and < 3 . For a plasmid the size of pUC18 , this means that the ligation
...
In summary , ligation reactions involving linearized phosphorylated plasmid DNA
with cohesive termini should contain : • Sufficient vector DNA to achieve a j : i
ratio of > 1 and < 3 . For a plasmid the size of pUC18 , this means that the ligation
...
Page 2-11
CHOOSING THE APPROPRIATE BACTERIOPHAGE , VECTOR There is no
single bacteriophage i vector suitable for cloning all DNA fragments . It is
therefore necessary to choose carefully among the available vectors for the one
best suited ...
CHOOSING THE APPROPRIATE BACTERIOPHAGE , VECTOR There is no
single bacteriophage i vector suitable for cloning all DNA fragments . It is
therefore necessary to choose carefully among the available vectors for the one
best suited ...
Page 2-82
Preparation of vector DNA by cleavage with appropriate restriction enzyme ( s ) .
2. Ligation of the digested vector with fragments of foreign DNA having termini
compatible with those of the vector . 3. Packaging of the ligated DNA into ...
Preparation of vector DNA by cleavage with appropriate restriction enzyme ( s ) .
2. Ligation of the digested vector with fragments of foreign DNA having termini
compatible with those of the vector . 3. Packaging of the ligated DNA into ...
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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