E. coli Plasmid Vectors: Methods and Applications
Manipulation of recombinant DNA, which is almost exclusively performed using the host E. coli, constitutes one of the fundamental methodologies of molecular biotechnology. In E. coli Plasmid Vectors, experienced bench researchers describe their proven techniques for the manipulation of recombinant p...
Gespeichert in:
| Weitere Verfasser: | , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Totowa, NJ
Humana Press
2003
|
| Schriftenreihe: | Methods in Molecular Biology™
235 |
| Schlagworte: | |
| Online-Zugang: | UBR01 TUM01 Volltext |
| Zusammenfassung: | Manipulation of recombinant DNA, which is almost exclusively performed using the host E. coli, constitutes one of the fundamental methodologies of molecular biotechnology. In E. coli Plasmid Vectors, experienced bench researchers describe their proven techniques for the manipulation of recombinant plasmids utilizing this popular bacterial host. The authors describe readily reproducible methods for cloning DNA into plasmid vectors, transforming plasmids into E. coli, and analyzing recombinant clones. They also include protocols for the construction and screening of libraries, as well as specific techniques for specialized cloning vehicles, such as cosmids, bacterial artificial chromosomes, l vectors, and phagemids. Also presented are methods for common downstream applications, such as mutagenesis, expression of recombinant proteins and RNA transcripts, and uses of reporter genes. Each fully tested protocol is described in step-by-step detail by an established expert in the field and includes an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, tips on troubleshooting and avoiding known pitfalls and, where needed, a discussion of the interpretation and use of the results. Comprehensive and highly practical, E. coli Plasmid Vectors offers those new to the field a basic guide to the use of plasmid vectors in the cloning host E. coli, and those more experienced researchers a broad-ranging, proven array of successful techniques |
| Beschreibung: | 1 Online-Ressource (XII, 316 p) |
| ISBN: | 9781592594092 |
| DOI: | 10.1385/1592594093 |
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| 520 | |a Manipulation of recombinant DNA, which is almost exclusively performed using the host E. coli, constitutes one of the fundamental methodologies of molecular biotechnology. In E. coli Plasmid Vectors, experienced bench researchers describe their proven techniques for the manipulation of recombinant plasmids utilizing this popular bacterial host. The authors describe readily reproducible methods for cloning DNA into plasmid vectors, transforming plasmids into E. coli, and analyzing recombinant clones. They also include protocols for the construction and screening of libraries, as well as specific techniques for specialized cloning vehicles, such as cosmids, bacterial artificial chromosomes, l vectors, and phagemids. Also presented are methods for common downstream applications, such as mutagenesis, expression of recombinant proteins and RNA transcripts, and uses of reporter genes. Each fully tested protocol is described in step-by-step detail by an established expert in the field and includes an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, tips on troubleshooting and avoiding known pitfalls and, where needed, a discussion of the interpretation and use of the results. Comprehensive and highly practical, E. coli Plasmid Vectors offers those new to the field a basic guide to the use of plasmid vectors in the cloning host E. coli, and those more experienced researchers a broad-ranging, proven array of successful techniques | ||
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| spelling | E. coli Plasmid Vectors Methods and Applications edited by Nicola Casali, Andrew Preston Totowa, NJ Humana Press 2003 1 Online-Ressource (XII, 316 p) txt rdacontent c rdamedia cr rdacarrier Methods in Molecular Biology™ 235 Manipulation of recombinant DNA, which is almost exclusively performed using the host E. coli, constitutes one of the fundamental methodologies of molecular biotechnology. In E. coli Plasmid Vectors, experienced bench researchers describe their proven techniques for the manipulation of recombinant plasmids utilizing this popular bacterial host. The authors describe readily reproducible methods for cloning DNA into plasmid vectors, transforming plasmids into E. coli, and analyzing recombinant clones. They also include protocols for the construction and screening of libraries, as well as specific techniques for specialized cloning vehicles, such as cosmids, bacterial artificial chromosomes, l vectors, and phagemids. Also presented are methods for common downstream applications, such as mutagenesis, expression of recombinant proteins and RNA transcripts, and uses of reporter genes. Each fully tested protocol is described in step-by-step detail by an established expert in the field and includes an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, tips on troubleshooting and avoiding known pitfalls and, where needed, a discussion of the interpretation and use of the results. Comprehensive and highly practical, E. coli Plasmid Vectors offers those new to the field a basic guide to the use of plasmid vectors in the cloning host E. coli, and those more experienced researchers a broad-ranging, proven array of successful techniques Life Sciences Biochemistry, general Cell Biology Life sciences Biochemistry Cell biology Escherichia coli (DE-588)4070959-0 gnd rswk-swf Labortechnik (DE-588)4123602-6 gnd rswk-swf Plasmid (DE-588)4046270-5 gnd rswk-swf 1\p (DE-588)4143413-4 Aufsatzsammlung gnd-content Escherichia coli (DE-588)4070959-0 s Plasmid (DE-588)4046270-5 s Labortechnik (DE-588)4123602-6 s DE-604 Casali, Nicola edt Preston, Andrew edt Erscheint auch als Druck-Ausgabe 9781588291516 https://doi.org/10.1385/1592594093 Verlag URL des Erstveröffentlichers Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | E. coli Plasmid Vectors Methods and Applications Life Sciences Biochemistry, general Cell Biology Life sciences Biochemistry Cell biology Escherichia coli (DE-588)4070959-0 gnd Labortechnik (DE-588)4123602-6 gnd Plasmid (DE-588)4046270-5 gnd |
| subject_GND | (DE-588)4070959-0 (DE-588)4123602-6 (DE-588)4046270-5 (DE-588)4143413-4 |
| title | E. coli Plasmid Vectors Methods and Applications |
| title_auth | E. coli Plasmid Vectors Methods and Applications |
| title_exact_search | E. coli Plasmid Vectors Methods and Applications |
| title_full | E. coli Plasmid Vectors Methods and Applications edited by Nicola Casali, Andrew Preston |
| title_fullStr | E. coli Plasmid Vectors Methods and Applications edited by Nicola Casali, Andrew Preston |
| title_full_unstemmed | E. coli Plasmid Vectors Methods and Applications edited by Nicola Casali, Andrew Preston |
| title_short | E. coli Plasmid Vectors |
| title_sort | e coli plasmid vectors methods and applications |
| title_sub | Methods and Applications |
| topic | Life Sciences Biochemistry, general Cell Biology Life sciences Biochemistry Cell biology Escherichia coli (DE-588)4070959-0 gnd Labortechnik (DE-588)4123602-6 gnd Plasmid (DE-588)4046270-5 gnd |
| topic_facet | Life Sciences Biochemistry, general Cell Biology Life sciences Biochemistry Cell biology Escherichia coli Labortechnik Plasmid Aufsatzsammlung |
| url | https://doi.org/10.1385/1592594093 |
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