Molecular Cloning: A Laboratory Manual, Volume 1 |
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Results 1-3 of 78
Page 2-13
progeny DNA molecules . However , the presence of an active bacterial
recombination system occasionally leads to rearrangements ( in particular to
deletion ) of segments of foreign DNA that carry repeated sequences ( see , e.g. ,
Lauer et al .
progeny DNA molecules . However , the presence of an active bacterial
recombination system occasionally leads to rearrangements ( in particular to
deletion ) of segments of foreign DNA that carry repeated sequences ( see , e.g. ,
Lauer et al .
Page 3-21
Both cosmids carry the SV40 origin of replication and sequences that enhance
the expression of cloned genes . The bacteriophage T3 and T7 promoters form
the basis of a simple method to prepare probes from the ends of large segments
of ...
Both cosmids carry the SV40 origin of replication and sequences that enhance
the expression of cloned genes . The bacteriophage T3 and T7 promoters form
the basis of a simple method to prepare probes from the ends of large segments
of ...
Page 5-50
This is accomplished using two oligonucleotide primers complementary to
sequences that flank the region of interest . The first oligonucleotide is
complementary to sequences of one strand of the template upstream of the
region of interest ...
This is accomplished using two oligonucleotide primers complementary to
sequences that flank the region of interest . The first oligonucleotide is
complementary to sequences of one strand of the template upstream of the
region of interest ...
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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