Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 2-94
TABLE 2.5 Amounts of Potential Insert DNA Used in Trial Ligations of
Bacteriophage 1 Arms Amount of potential insert Size ( kb ) of potential insert
DNA DNA to be used in trial ligations 2-4 4-8 8-12 12-16 16-20 20-24 6-200 ng
12-400 ng ...
TABLE 2.5 Amounts of Potential Insert DNA Used in Trial Ligations of
Bacteriophage 1 Arms Amount of potential insert Size ( kb ) of potential insert
DNA DNA to be used in trial ligations 2-4 4-8 8-12 12-16 16-20 20-24 6-200 ng
12-400 ng ...
Page 5-32
Keep reaction volumes to a minimum by reducing the amount of water in the
reaction as much as possible . However , make sure that the restriction enzyme
contributes less than 0.1 volume of the final reaction mixture ; otherwise , the
enzyme ...
Keep reaction volumes to a minimum by reducing the amount of water in the
reaction as much as possible . However , make sure that the restriction enzyme
contributes less than 0.1 volume of the final reaction mixture ; otherwise , the
enzyme ...
Page 7-37
These include : • Northern hybridization ( RNA blotting ) , in which the size and
amount of specific mRNA molecules in preparations of total or poly ( A ) * RNA
are determined ( Alwine et al . 1977 , 1979 ) . The RNA is separated according to
...
These include : • Northern hybridization ( RNA blotting ) , in which the size and
amount of specific mRNA molecules in preparations of total or poly ( A ) * RNA
are determined ( Alwine et al . 1977 , 1979 ) . The RNA is separated according to
...
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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