Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 2-23
There is no selection for recombinants . It is also possible to use this vector as a
substitution vector for EcoRI - Sall , Sall - Xhol , and EcoRI - BamHI fragments . In
these cases , the recombinants must be propagated on recA * hosts because ...
There is no selection for recombinants . It is also possible to use this vector as a
substitution vector for EcoRI - Sall , Sall - Xhol , and EcoRI - BamHI fragments . In
these cases , the recombinants must be propagated on recA * hosts because ...
Page 3-18
COSMITID VECTORS FOR TRANSFECTION OF MAMMALIAN CELLS Several
cosmid vectors have been developed to shuttle genes into and out of mammalian
cells and to isolate eukaryotic genes by functional selection . These vectors differ
...
COSMITID VECTORS FOR TRANSFECTION OF MAMMALIAN CELLS Several
cosmid vectors have been developed to shuttle genes into and out of mammalian
cells and to isolate eukaryotic genes by functional selection . These vectors differ
...
Page 1-2
See also Antibiotics ; Selection Aminopterin , selection , 3.18 , 16.9 . See also
HAT medium ; Selection Ammonium acetate , stock solution , B.10 Ammonium
hydroxide common commercial strengths , B.2 pH values of stock solutions , B.3 ...
See also Antibiotics ; Selection Aminopterin , selection , 3.18 , 16.9 . See also
HAT medium ; Selection Ammonium acetate , stock solution , B.10 Ammonium
hydroxide common commercial strengths , B.2 pH values of stock solutions , B.3 ...
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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