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The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers

Author

Joachim Messing

1946 - 2019

Published in: Gene

Date of publication: 1982-10-01

Language: English

Bibliographic databases:

Cites articles 15

Date

Title

Authors

1976-04-01

Characterization of a mini-ColC1 plasmid
1977

Construction and characterization of new cloning vehicles. II. A multipurpose cloning system,Construction and characterization of new cloning vehicle. II. A multipurpose cloning system
1978-03-01

Methylation of single-stranded DNA in vitro introduces new restriction endonuclease cleavage sites
1978-05-01

Extracellular nucleases of pseudomonas BAL 31. III. Use of the double-strand deoxyriboexonuclease activity as the basis of a convenient method for the mapping of fragments of DNA produced by cleavage with restriction enzymes,Extracellular nucleases of Pseudomonas BAL 31. III. Use of the double-strand deoxyriboexonuclease activity as the basis of a convenient method for the mapping of fragments of DNA produced by cleavage with restriction enzymes
1979-03-01

The use of exonuclease III for preparing single stranded DNA for use as a template in the chain terminator sequencing method
1979-04-01

Sequence of the gene for iso-l-cytochrome c in saccharomyces cerevisiae
1980-06-01

A versatile primer for DNA sequencing in the M13mp2 cloning system
1980-01-01

Construction and properties of a new cloning vehicle, allowing direct sereening for recombinant plasmids
1981-03-01

A method for sequencing single-stranded cloned DNA in both directions
1981-07-01

Nucleotide sequence of naturally occurring deletion mutants of cauliflower mosaic virus

,
1981-01-01

A system for shotgun DNA sequencing
1981-04-01

Nucleotide sequence of the kanamycin resistance transposon Tn903
1981-12-01

A set of synthetic oligodeoxyribonucleotide primers for DNA sequencing in the plasmid vector pBR322
1982-03-01

The making of strand-specific M13 probes
1982-10

A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments

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