Molecular Cloning: A Laboratory Manual, Volume 1 |
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Results 1-3 of 86
Page 168
Redissolve the DNAs in TE ( pH 7.6 ) at a concentration of 100 ug / ml . 2. Set up
the ligation mixtures as follows : a . Transfer 0.1 ug of the vector DNA to a sterile
microfuge tube . Add an equimolar amount of foreign DNA . b . Add H , O to 7.5 ul
...
Redissolve the DNAs in TE ( pH 7.6 ) at a concentration of 100 ug / ml . 2. Set up
the ligation mixtures as follows : a . Transfer 0.1 ug of the vector DNA to a sterile
microfuge tube . Add an equimolar amount of foreign DNA . b . Add H , O to 7.5 ul
...
Page 3-41
Spread 0.5 ml and 0.1 ml of the bacterial culture onto TB agar plates containing
ampicillin ( 50 ug / ml ) . After incubating the plates overnight at 37 ° C , count the
number of bacterial colonies . Each microgram of ligated cosmid - eukaryotic ...
Spread 0.5 ml and 0.1 ml of the bacterial culture onto TB agar plates containing
ampicillin ( 50 ug / ml ) . After incubating the plates overnight at 37 ° C , count the
number of bacterial colonies . Each microgram of ligated cosmid - eukaryotic ...
Page 4-48
Add kanamycin ( 25 mg / ml in H20 ) to a final concentration of 70 ug / ml .
Continue incubation for a further 14-18 hours at 37 ° C . The yield of virus
particles containing single - stranded copies of the plasmid can be measured by
infecting ...
Add kanamycin ( 25 mg / ml in H20 ) to a final concentration of 70 ug / ml .
Continue incubation for a further 14-18 hours at 37 ° C . The yield of virus
particles containing single - stranded copies of the plasmid can be measured by
infecting ...
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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