Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 5-14
ISOSCHIZOMERS In general , different restriction enzymes recognize different
sequences ( see Table 5.1 ) . However , there are many examples of enzymes
isolated from different sources that cleave within the same target sequences .
ISOSCHIZOMERS In general , different restriction enzymes recognize different
sequences ( see Table 5.1 ) . However , there are many examples of enzymes
isolated from different sources that cleave within the same target sequences .
Page 5-15
For most purposes , this problem can be avoided by using Bst NI , which
recognizes exactly the same sequence as ... at least three different methylation -
dependent restriction systems that recognize different target sequences only
when ...
For most purposes , this problem can be avoided by using Bst NI , which
recognizes exactly the same sequence as ... at least three different methylation -
dependent restriction systems that recognize different target sequences only
when ...
Page 1-35
generation of probes , 14.6–14.8 inverse , for amplification of segments flanking
target sequence , 14.1214.13 methods ... to prevent contamination , 14.14
quantitation of concentration of target sequences , 14.30-14.33 reaction
components ...
generation of probes , 14.6–14.8 inverse , for amplification of segments flanking
target sequence , 14.1214.13 methods ... to prevent contamination , 14.14
quantitation of concentration of target sequences , 14.30-14.33 reaction
components ...
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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