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Francisco Bolívar

Researcher at National Autonomous University of Mexico

Publications -  176
Citations -  17774

Francisco Bolívar is an academic researcher from National Autonomous University of Mexico. The author has contributed to research in topics: Escherichia coli & Gene. The author has an hindex of 50, co-authored 173 publications receiving 17121 citations. Previous affiliations of Francisco Bolívar include Centra & Genentech.

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Construction and characterization of new cloning vehicles. II. A multipurpose cloning system.

TL;DR: In vitro recombination techniques were used to construct a new cloning vehicle, pBR322, which is a relaxed replicating plasmid, does not produce and is sensitive to colicin E1, and carries resistance genes to the antibiotics ampicillin (Ap) and tetracycline (Tc).
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Construction and characterization of new cloning vehicles. I. Ampicillin-resistant derivatives of the plasmid pMB9.

TL;DR: In vitro recombination via restriction endonucleases and the in vivo genetic translocation of the Ap resistance (Apr) gene resulted in the construction of a new cloning vehicle, the plasmid pBR313, which has a molecular weight of 5.8 Mdalton and has been characterized using thirteen restriction enzymes, six of which cleave the plasid at unique restriction sites.
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Expression in Escherichia coli of a Chemically Synthesized Gene for the Hormone Somatostatin

TL;DR: This work has reported the first synthesis of a functional polypeptide product from a gene of chemically synthesized origin, including the sequence of amino acids corresponding to somatostatin, in vitro.
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Expression in Escherichia coli of chemically synthesized genes for human insulin

TL;DR: Synthetic genes for human insulin A and B chains were cloned separately in plasmid pBR322 and fused to an Escherichia coli beta-galactosidase gene to provide efficient transcription and translation and a stable precursor protein.
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Construction and characterization of new cloning vehicles. III. Derivatives of plasmid pBR322 carrying unique Eco RI sites for selection of Eco RI generated recombinant DNA molecules.

TL;DR: In vitro recombinant DNA techniques were used to construct two new cloning vehicles, pBR324 and pBR235, which permit the molecular cloning and easy selection of EcoRI, BamHI, HindIII, PstI, HincII, SalI, (XamI), Smal, ( XmaI), BglII and DpnII restriction generated DNA molecules.