Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 6-22
Inefficient recovery of large fragments of DNA . The efficiency with which DNA is
recovered from agarose gels is a function of its molecular weight . Although most
methods give reasonable yields of DNA fragments that are less than 5 kb in ...
Inefficient recovery of large fragments of DNA . The efficiency with which DNA is
recovered from agarose gels is a function of its molecular weight . Although most
methods give reasonable yields of DNA fragments that are less than 5 kb in ...
Page 6-47
It is convenient if the volume of elution buffer is no greater than 0.5 ml , since the
eluted fragment of DNA can then be precipitated with ethanol ... Small fragments
of DNA ( < 500 bp ) are eluted in 3–4 hours ; larger fragments take 12–16 hours .
It is convenient if the volume of elution buffer is no greater than 0.5 ml , since the
eluted fragment of DNA can then be precipitated with ethanol ... Small fragments
of DNA ( < 500 bp ) are eluted in 3–4 hours ; larger fragments take 12–16 hours .
Page 6-49
In the past , such separated fragments were obtained by electrophoresis of
denatured DNA through neutral agarose gels ( Hayward 1972 ; Tibbetts et al .
1974 ; Dunn and Sambrook 1980 ) or polyacrylamide gels ( Maxam and Gilbert
1977 ...
In the past , such separated fragments were obtained by electrophoresis of
denatured DNA through neutral agarose gels ( Hayward 1972 ; Tibbetts et al .
1974 ; Dunn and Sambrook 1980 ) or polyacrylamide gels ( Maxam and Gilbert
1977 ...
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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