Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 6-7
Electrophoresis buffers are usually made up as concentrated solutions and
stored at room temperature . For historical reasons , TAE is the most commonly
used buffer . However , its buffering capacity is rather low , and it tends to become
...
Electrophoresis buffers are usually made up as concentrated solutions and
stored at room temperature . For historical reasons , TAE is the most commonly
used buffer . However , its buffering capacity is rather low , and it tends to become
...
Page 7-27
equal amount of 2 x column - loading buffer . Apply the solution to the column ,
and immediately begin to collect the eluate in a sterile tube . When all of the RNA
solution has entered the column , add 1 column volume of 1 x column - loading ...
equal amount of 2 x column - loading buffer . Apply the solution to the column ,
and immediately begin to collect the eluate in a sterile tube . When all of the RNA
solution has entered the column , add 1 column volume of 1 x column - loading ...
Page 1-45
See DNA - binding proteins in vitro DNA templates , 10.31 synthesis of RNA
probes by DNAdependent RNA polymerases , 10.27-10.37 synthesis of synthetic
mRNAs , 18.82-18.84 transcription buffer , 10.33 promoters . See Promoters ...
See DNA - binding proteins in vitro DNA templates , 10.31 synthesis of RNA
probes by DNAdependent RNA polymerases , 10.27-10.37 synthesis of synthetic
mRNAs , 18.82-18.84 transcription buffer , 10.33 promoters . See Promoters ...
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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
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