Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 5-36
The RNAase H activity is essential for cell viability in E. coli but has not been
used in molecular cloning . USES 1. Labeling of DNA by nick translation ( see
Figure 5.2 ) . Of all the polymerases , only E. coli DNA polymerase I can carry out
this ...
The RNAase H activity is essential for cell viability in E. coli but has not been
used in molecular cloning . USES 1. Labeling of DNA by nick translation ( see
Figure 5.2 ) . Of all the polymerases , only E. coli DNA polymerase I can carry out
this ...
Page 5-42
E. coli DNA Polymerase I Klenow Fragment Activity : 5'3 ' DNA polymerase
Substrate : Single - stranded DNA template with a primer containing a free 3 ' -
hydroxyl group . Reaction : Klenow fragment of E. coli DNA polymerase ! DNAOH
DNA ...
E. coli DNA Polymerase I Klenow Fragment Activity : 5'3 ' DNA polymerase
Substrate : Single - stranded DNA template with a primer containing a free 3 ' -
hydroxyl group . Reaction : Klenow fragment of E. coli DNA polymerase ! DNAOH
DNA ...
Page 5-52
The murine and avian reverse transcriptases differ from one another in a number
of respects : • The avian enzyme consists of two polypeptide chains that carry
both a polymerase activity and a powerful RNAase H activity ( Verma 1981 ) .
The murine and avian reverse transcriptases differ from one another in a number
of respects : • The avian enzyme consists of two polypeptide chains that carry
both a polymerase activity and a powerful RNAase H activity ( Verma 1981 ) .
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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