Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 162
Test Ligations and Transformations The best way to assay whether
dephosphorylation has been successful is to set up a series of ... Plate 1 , 10 ,
and 50 ul of each of the transformation reactions on plates containing the
appropriate antibiotic .
Test Ligations and Transformations The best way to assay whether
dephosphorylation has been successful is to set up a series of ... Plate 1 , 10 ,
and 50 ul of each of the transformation reactions on plates containing the
appropriate antibiotic .
Page 175
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis.
Transformation of E. coli by High - voltage Electroporation ( Electrotransformation
) The method of electroporation was developed originally to introduce DNA into
eukaryotic ...
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis.
Transformation of E. coli by High - voltage Electroporation ( Electrotransformation
) The method of electroporation was developed originally to introduce DNA into
eukaryotic ...
Page 176
Protocol I : Preparation of Fresh or Frozen Competent E. coli The following
procedure , which was developed by Hanahan ( 1983 ) , can yield competent
cultures of E. coli strains DH1 , DH5 , and MM294 that can be transformed at
frequencies ...
Protocol I : Preparation of Fresh or Frozen Competent E. coli The following
procedure , which was developed by Hanahan ( 1983 ) , can yield competent
cultures of E. coli strains DH1 , DH5 , and MM294 that can be transformed at
frequencies ...
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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