Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 178
The solution is sterilized by filtration through a disposable Nalgene filter ( 0.45 -
micron pore size ) , divided into 10 - ml aliquots , and stored frozen at -20 ° C .
Prepare the TFB by mixing all of the components with 800 ml of pure H , 0.5
Adjust ...
The solution is sterilized by filtration through a disposable Nalgene filter ( 0.45 -
micron pore size ) , divided into 10 - ml aliquots , and stored frozen at -20 ° C .
Prepare the TFB by mixing all of the components with 800 ml of pure H , 0.5
Adjust ...
Page 179
Dispense 160 - ul aliquots of the DnD solution into sterile 0.5 - ml microfuge
tubes . Close the tubes tightly and ... ml aliquots in sterile tubes . The tubes
should be closed tightly and stored at - 70 ° C . Each aliquot should be used only
once and ...
Dispense 160 - ul aliquots of the DnD solution into sterile 0.5 - ml microfuge
tubes . Close the tubes tightly and ... ml aliquots in sterile tubes . The tubes
should be closed tightly and stored at - 70 ° C . Each aliquot should be used only
once and ...
Page 180
Working quickly , dispense aliquots of the suspensions into chilled , sterile
microfuge tubes . Immediately snap - freeze the competent cells by immersing the
tightly closed tubes in liquid nitrogen . Store the tubes at – 70 ° C until needed .
Working quickly , dispense aliquots of the suspensions into chilled , sterile
microfuge tubes . Immediately snap - freeze the competent cells by immersing the
tightly closed tubes in liquid nitrogen . Store the tubes at – 70 ° C until needed .
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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