Molecular Cloning: A Laboratory Manual, Volume 1 |
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Results 1-3 of 87
Page 1-101
Hybridization to Nitrocellulose Filters Containing Replicas of Bacterial Colonies
The following protocol is designed for 30 circular nitrocellulose filters , 82 mm in
diameter . Appropriate adjustments to the volumes should be made when
carrying ...
Hybridization to Nitrocellulose Filters Containing Replicas of Bacterial Colonies
The following protocol is designed for 30 circular nitrocellulose filters , 82 mm in
diameter . Appropriate adjustments to the volumes should be made when
carrying ...
Page 2-110
Once in contact with the top agarose , the filter wets very rapidly and transfer of
bacteriophage DNA occurs quickly . ... has developed the following procedure to
fix bacteriophagea DNA to nitrocellulose filters that avoids treating filters with ...
Once in contact with the top agarose , the filter wets very rapidly and transfer of
bacteriophage DNA occurs quickly . ... has developed the following procedure to
fix bacteriophagea DNA to nitrocellulose filters that avoids treating filters with ...
Page 2-113
Incubate the replica plates at 37 ° C until a thick bacterial lawn with clearly visible
plaques has appeared on the filter ( 5–12 hours ) . If the bacterial lawn is not ...
Bacterial growth is more rapid on nitrocellulose filters than on nylon membranes .
Incubate the replica plates at 37 ° C until a thick bacterial lawn with clearly visible
plaques has appeared on the filter ( 5–12 hours ) . If the bacterial lawn is not ...
Bacterial growth is more rapid on nitrocellulose filters than on nylon membranes .
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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