A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, AccI, HindII, BamHI and EcoRI) in a small region of its lac Z-gene part. Insertion of foreign DNA into the plasmid can be easily detected. Bacteria harbouring recombinant plasmids generally give rise to white colonies, while those containing only vector DNA form blue colonies on indicator plates. Plasmid DNA purified by a rapid method (Birnboim, H.C. and Doly, J. (1979) Nucl. Acids. Res. 7, 1513-1523) can be used for chemical sequencing of the cloned insert DNA. Labeled fragments need not be isolated after cutting with the proper restriction enzymes and are treated directly according to the sequencing protocol of Maxam and Gilbert
<p>(A) The vector pUC19 was prepared by PCR with the primers dest-f and dest-r. The fragment D1 (red...
Biochemical, biophysical and genetic studies of DNA segments of complex genomes are greatly facilita...
A rapid method for constructing new cloning vectors was described. The special features taken for mu...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, Sail, A...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
We have constructed a plasmid cloning vector, pGB2, which is derived from the Escherichia coli plasm...
International audiencePlasmids play a central role in engineering recombinant bacteria because they ...
International audiencePlasmids play a central role in engineering recombinant bacteria because they ...
The method uses a novel plasmid vector, p9lox5, containing a site-specific recombination sequence lo...
Introducing PCR products into plasmids vectors is key for molecular techniques. Ideally cloning vect...
Replicons from bifidobacteria species are required for the construction of general- and special-purp...
<p>(A) The vector pUC19 was prepared by PCR with the primers dest-f and dest-r. The fragment D1 (red...
Biochemical, biophysical and genetic studies of DNA segments of complex genomes are greatly facilita...
A rapid method for constructing new cloning vectors was described. The special features taken for mu...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, SalI, A...
A multipurpose plasmid, pUR222, was constructed. It contains six unique cloning sites (PstI, Sail, A...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
We have constructed a plasmid cloning vector, pGB2, which is derived from the Escherichia coli plasm...
International audiencePlasmids play a central role in engineering recombinant bacteria because they ...
International audiencePlasmids play a central role in engineering recombinant bacteria because they ...
The method uses a novel plasmid vector, p9lox5, containing a site-specific recombination sequence lo...
Introducing PCR products into plasmids vectors is key for molecular techniques. Ideally cloning vect...
Replicons from bifidobacteria species are required for the construction of general- and special-purp...
<p>(A) The vector pUC19 was prepared by PCR with the primers dest-f and dest-r. The fragment D1 (red...
Biochemical, biophysical and genetic studies of DNA segments of complex genomes are greatly facilita...
A rapid method for constructing new cloning vectors was described. The special features taken for mu...