Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page iv
We wish particularly to thank Arg Efstratiadis for his helpful discussions and
criticisms of Chapter 7 ; Brian Seed for permission to include a description of his
unpublished procedure for screening libraries by recombination ( Chapter 10 )
and ...
We wish particularly to thank Arg Efstratiadis for his helpful discussions and
criticisms of Chapter 7 ; Brian Seed for permission to include a description of his
unpublished procedure for screening libraries by recombination ( Chapter 10 )
and ...
Page vi
In an attempt to counteract this trend , we have greatly increased the amount of
background material at the beginning of each chapter of the manual and we have
provided full references . Users of the manual who read this material should ...
In an attempt to counteract this trend , we have greatly increased the amount of
background material at the beginning of each chapter of the manual and we have
provided full references . Users of the manual who read this material should ...
Page 109
This allows copies of one of the two strands of the plasmid DNA to be produced
in quantities sufficient for sequencing ( see Chapter 13 ) or for preparation of
radiolabeled single - stranded probes ( see Chapter 10 ) . Plasmid Vectors
Carrying ...
This allows copies of one of the two strands of the plasmid DNA to be produced
in quantities sufficient for sequencing ( see Chapter 13 ) or for preparation of
radiolabeled single - stranded probes ( see Chapter 10 ) . Plasmid Vectors
Carrying ...
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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