Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 84
Page xxiv
... MEMBRANES UNDER NEUTRAL CONDITIONS 9.44 CAPILLARY TRANSFER
OF DNA TO NYLON MEMBRANES UNDER ALKALINE CONDITIONS 9.45
HYBRIDIZATION OF RADIOLABELED PROBES TO IMMOBILIZED NUCLEIC
ACIDS ...
... MEMBRANES UNDER NEUTRAL CONDITIONS 9.44 CAPILLARY TRANSFER
OF DNA TO NYLON MEMBRANES UNDER ALKALINE CONDITIONS 9.45
HYBRIDIZATION OF RADIOLABELED PROBES TO IMMOBILIZED NUCLEIC
ACIDS ...
Page xxv
SYNTHESIS OF RNA PROBES BY IN VITRO TRANSCRIPTION OF
DOUBLESTRANDED DNA TEMPLATES BY BACTERIOPHAGE DNA -
DEPENDENT RNA POLYMERASES 10.27 Plasmid Vectors for Preparing RNA
Probes 10.29 ...
SYNTHESIS OF RNA PROBES BY IN VITRO TRANSCRIPTION OF
DOUBLESTRANDED DNA TEMPLATES BY BACTERIOPHAGE DNA -
DEPENDENT RNA POLYMERASES 10.27 Plasmid Vectors for Preparing RNA
Probes 10.29 ...
Page 1-12
... of radioactive probes, 10.20-10.21 repair of DNA to create blunt end, 8.27,
17.20-17.23 synthesis of single-stranded DNA probes, 10.22-10.24 synthesis of
uniformly labeled DNA probes using random oligonucleotide primers, 10.13-
10.17 ...
... of radioactive probes, 10.20-10.21 repair of DNA to create blunt end, 8.27,
17.20-17.23 synthesis of single-stranded DNA probes, 10.22-10.24 synthesis of
uniformly labeled DNA probes using random oligonucleotide primers, 10.13-
10.17 ...
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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