Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 4-28
The yield of RF DNA expected from 1 ml of an infected bacterial culture is usually
~ 500 ng , which is enough for five digests . Note This method , devised by
Birnboim and Doly ( 1979 ) and subsequently modified by Ish - Horowicz and
Burke ...
The yield of RF DNA expected from 1 ml of an infected bacterial culture is usually
~ 500 ng , which is enough for five digests . Note This method , devised by
Birnboim and Doly ( 1979 ) and subsequently modified by Ish - Horowicz and
Burke ...
Page 6-15
Usually , 10-100 ng of DNA , in the gel - loading buffer of choice , are applied to a
slot . The gel is run for 30-60 minutes at high voltage ( 5–20 V / cm ) until the
bromophenol blue and xylene cyanol FF have migrated the appropriate distance
.
Usually , 10-100 ng of DNA , in the gel - loading buffer of choice , are applied to a
slot . The gel is run for 30-60 minutes at high voltage ( 5–20 V / cm ) until the
bromophenol blue and xylene cyanol FF have migrated the appropriate distance
.
Page 7-40
Although the resolving powers of the two gel systems are approximately equal (
Miller 1987 ) , the bands of RNA detected by northern hybridization are usually
sharper when the RNA has been fractionated through gels containing glyoxal ...
Although the resolving powers of the two gel systems are approximately equal (
Miller 1987 ) , the bands of RNA detected by northern hybridization are usually
sharper when the RNA has been fractionated through gels containing glyoxal ...
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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