Molecular Cloning: A Laboratory Manual, Volume 1 |
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Results 1-3 of 75
Page 2-28
KH54 rex " cl 38880 Bgli 38820 Bghi 38170 Bgli 37940 Prul 37860 BGHI 23
WRA 35790 Pvut 35710 Boll WL113 34500 BamHI 34830 Sal 34590 San 34070
Sall 36140 Sall 35150 EcoRI 35140 Sacl Smal 35130 Xbal 35120 Sall 35100
Hindili ...
KH54 rex " cl 38880 Bgli 38820 Bghi 38170 Bgli 37940 Prul 37860 BGHI 23
WRA 35790 Pvut 35710 Boll WL113 34500 BamHI 34830 Sal 34590 San 34070
Sall 36140 Sall 35150 EcoRI 35140 Sacl Smal 35130 Xbal 35120 Sall 35100
Hindili ...
Page 2-33
These vectors are particularly useful for cloning Sau 3AI partial digests , as the
BamHI sites in the vectors are flanked by EcoRI and Sall sites . Cloned fragments
can therefore be excised from the recombinants by digestion with Sall or EcoRI .
These vectors are particularly useful for cloning Sau 3AI partial digests , as the
BamHI sites in the vectors are flanked by EcoRI and Sall sites . Cloned fragments
can therefore be excised from the recombinants by digestion with Sall or EcoRI .
Page 2-45
The two natural bacteriophage Sall sites were destroyed by digesting igt11 with
Sall and then ligating the bacteriophage 1 arms in the presence of an
oligonucleotide that does not reconstruct the Sall sites . This alteration causes the
vector to ...
The two natural bacteriophage Sall sites were destroyed by digesting igt11 with
Sall and then ligating the bacteriophage 1 arms in the presence of an
oligonucleotide that does not reconstruct the Sall sites . This alteration causes the
vector to ...
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User Review - iayork - LibraryThingthe BIBLE of every biologist: So few and so much to say about this bible of Biology at the bench... You'll really find everything you want in it, including the composition of all the buffers and ... Read full review
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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