Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 174
Many variations of this basic technique have since been described , all directed
toward optimizing the efficiency of transformation of different bacterial strains by
plasmids . Bacteria treated according to the original protocol of Mandel and Higa
...
Many variations of this basic technique have since been described , all directed
toward optimizing the efficiency of transformation of different bacterial strains by
plasmids . Bacteria treated according to the original protocol of Mandel and Higa
...
Page 175
Transformation efficiencies of 10 ' - 1010 transformants / ug of DNA have been
achieved by optimizing various ... In general , the authors claim that the efficiency
of electrotransformation is 10 to 20 times higher than that obtained with
maximally ...
Transformation efficiencies of 10 ' - 1010 transformants / ug of DNA have been
achieved by optimizing various ... In general , the authors claim that the efficiency
of electrotransformation is 10 to 20 times higher than that obtained with
maximally ...
Page 176
Because the presence of trace amounts of detergent or other chemicals greatly
reduces the efficiency of bacterial transformation , it is best to set aside a batch of
glassware that is used for no other purpose than to prepare competent bacteria .
Because the presence of trace amounts of detergent or other chemicals greatly
reduces the efficiency of bacterial transformation , it is best to set aside a batch of
glassware that is used for no other purpose than to prepare competent bacteria .
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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