Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 2-12
However , if the cl gene has been inactivated by insertion of foreign DNA , the
growth of the bacteriophage is not restricted in hfl cells and the yield of progeny
particles is high . This property is extremely useful when constructing
recombinant ...
However , if the cl gene has been inactivated by insertion of foreign DNA , the
growth of the bacteriophage is not restricted in hfl cells and the yield of progeny
particles is high . This property is extremely useful when constructing
recombinant ...
Page 2-58
... For growth of Spi bacteriophage Used for production of high - titer lysates For
growth of Spi bacteriophage Will modify but not restrict DNA Used for
bacteriophage AORF8 libraries when Alul methylation is used Permissive for
growth of agt11 ...
... For growth of Spi bacteriophage Used for production of high - titer lysates For
growth of Spi bacteriophage Will modify but not restrict DNA Used for
bacteriophage AORF8 libraries when Alul methylation is used Permissive for
growth of agt11 ...
Page 4-15
( 1984 ) Used for growth of phagemids Will modify but not restrict transfected
DNA recA strain Carries episome conferring resistance to kanamycin Used for
growth of phagemids 71/18 Dente et al . ( 1983 ) KK2186 Zagursky and Berman (
1984 ) ...
( 1984 ) Used for growth of phagemids Will modify but not restrict transfected
DNA recA strain Carries episome conferring resistance to kanamycin Used for
growth of phagemids 71/18 Dente et al . ( 1983 ) KK2186 Zagursky and Berman (
1984 ) ...
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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