Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 108
Furthermore , fragments inserted at one restriction site can often be excised by
cleavage of the recombinant plasmid with restriction enzymes that cleave at
flanking sites . Insertion of a segment of DNA into a polycloning site is therefore ...
Furthermore , fragments inserted at one restriction site can often be excised by
cleavage of the recombinant plasmid with restriction enzymes that cleave at
flanking sites . Insertion of a segment of DNA into a polycloning site is therefore ...
Page 2-11
It is therefore important to choose a combination of vector and foreign DNA such
that the size of the recombinant bacteriophage falls within acceptable limits .
These constraints can sometimes be turned to advantage . After the central "
stuffer ...
It is therefore important to choose a combination of vector and foreign DNA such
that the size of the recombinant bacteriophage falls within acceptable limits .
These constraints can sometimes be turned to advantage . After the central "
stuffer ...
Page 3-5
Bacteria carrying recombinant cosmids can therefore be selected using media
containing the appropriate antibiotic . The packaging process can also be used to
transduce a recombinant cosmid from one bacterial host to another . Either a ...
Bacteria carrying recombinant cosmids can therefore be selected using media
containing the appropriate antibiotic . The packaging process can also be used to
transduce a recombinant cosmid from one bacterial host to another . Either a ...
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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