pcr cloning protocols (15 Ergebnisse)

Paperback. Zustand: Good. No Jacket. Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less.

Spiralbuch. Zustand: Gut. 490 Seiten Der Erhaltungszustand des hier angebotenen Werks ist trotz seiner Bibliotheksnutzung altersentsprechend sauber. Es befindet sich neben dem Rückenschild lediglich ein Bibliotheksstempel im Buch; ordnungsgemäß entwidmet. Untere Einbandkante leicht bestoßen. In ENGLISCHER Sprache. Sprache: Englisch Gewicht in Gramm: 650.

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Softcover/Paperback. Zustand: Sehr gut. 2nd ed. 453 p. Very good. Shrink wrapped. / Sehr guter Zustand. In Folie verschweißt. Sprache: Englisch Gewicht in Gramm: 834.

Zustand: Gut. Ausgabe: 2., Ed., 2002 Umfang/Format: 460 Seiten , 229 mm x 152 mm Einbandart und Originalverkaufspreis: : EUR 85.55 (unverbindliche Preisempfehlung), sfr 131.00 (unverbindliche Preisempfehlung) 0-89603-973-0 : EUR 85.55 (unverbindliche Preisempfehlung), sfr 131.00 (unverbindliche Preisempfehlung) PCR Cloning Protocols, Second Edition, updates and expands Bruce White, s best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination, and to clone the challenging uncharacterized DNA f Rutgers University, New. Brunswick From Reviews of the First Edition: .a balanced and easy to use guide to the principal contemporary options. Microbiology Today .eliminatles] mang laborious and expensive techniques associated with traditional Isolation and analysis. Biochemical Education In the post-genomic era, PCR has become the method of choice not only for cloning existing genes, but also for generating a wide array of novel genes hy mutagenesis and/or recombination within the genes of interest. PCR Cloning Protocols, Second Edition, updates and expands Bruce White, s best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis an long-distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination and to clone the challenging uncharacterized DNA flanking a known DNA fragment. Powerful applications of PCR in library construction and sublibrary generation and screening are also presented. Authoritative and up-to-date, PCR Cloning Protocols, Second Edition, constitutes a gold-standard collection of the fastest, simplest, and most popular methods for isolating genes from all biological samples and creating novel genes from them by mutagenesis/recombination essential methods for today, s study of functional genomics, gene expression, protein structure function relationships, protein engineering, and molecular evolution. Readily reproducible methods for isolating genes from all biological samples Cutting-edge techniques described by hands-on masters Azffiffleses Proven methods for cloning uncharacterized DNA z- flanking a known DNA fragment 111 Tested techniques for in vitro DNA recombination Part I. Performing and Optimizing PCR. Part II. Clon- bination. Part IV. Cloning Unknown Neighboring ing PCR Products. Part III. Mutagenesis and Recom- DNA. Part V. Library Construction and Screening. gutes Exemplar, ordentlich, Gern können sie Ihr Buch per Rechnung bestellen. Hardcover.

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Zustand: Sehr gut. Zustand: Sehr gut | Seiten: 439 | Sprache: Englisch | Produktart: Bücher | In the post-genomic era, PCR has become the method of choice not only for cloning existing genes, but also for generating a wide array of novel genes by mutagenesis and/or recombination within the genes of interest. PCR Cloning Protocols, Second Edition, updates and expands Bruce White's best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long-distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination and to clone the challenging uncharacterized DNA flanking a known DNA fragment. Powerful applications of PCR in library construction and sublibrary generation and screening are also presented. Authoritative and up-to-date, PCR Cloning Protocols, Second Edition, constitutes a gold-standard collection of the fastest, simplest, and most popular methods for isolating genes from all biological samples and creating novel genes from them by mutagenesis/recombination-essential methods for today's study of functional genomics, gene expression, protein structure-function relationships, protein engineering, and molecular evolution.

Zustand: Good. Your purchase helps support Sri Lankan Children's Charity 'The Rainbow Centre'. Ex-library, so some stamps and wear, but in good overall condition. Our donations to The Rainbow Centre have helped provide an education and a safe haven to hundreds of children who live in appalling conditions.

Gebunden. Zustand: New. Includes supplementary material: sn.pub/extrasPCR Cloning Protocols, Second Edition, updates and expands Bruce White s best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will .

Zustand: New. Editor(s): Chen, Bing-Yuan; Janes, Harry W. Series: Methods in Molecular Biology. Num Pages: 453 pages, biography. BIC Classification: PSF. Category: (P) Professional & Vocational. Dimension: 235 x 155 x 25. Weight in Grams: 665. . 2010. 2nd ed. Softcover of orig. ed. 2002. Paperback. . . . . Books ship from the US and Ireland.

Zustand: New. Provides methods for various aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long distance PCR and GC-rich template amplification. Editor(s): Chen, Bing-Yuan; Janes, Harry W. Series: Methods in Molecular Biology. Num Pages: 453 pages, biography. BIC Classification: PSAK. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 28. Weight in Grams: 1600. . 2002. 2nd ed. 2002. Hardback. . . . . Books ship from the US and Ireland.

Buch. Zustand: Neu. Neuware - PCR Cloning Protocols, Second Edition, updates and expands Bruce White's best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination, and to clone the challenging uncharacterized DNA flanking a known DNA fragment. In the post-genomic era, PCR has become the method of choice not only for cloning existing genes, but also for generating a wide array of novel genes by mutagenesis and/or recombination within the genes of interest. PCR Cloning Protocols, Second Edition, updates and expands Bruce White's best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long-distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination and to clone the challenging uncharacterized DNA flanking a known DNA fragment. Powerful applications of PCR in library construction and sublibrary generation and screening are also presented. Authoritative and up-to-date, PCR Cloning Protocols, Second Edition, constitutes a gold-standard collection of the fastest, simplest, and most popular methods for isolating genes from all biological samples and creating novel genes from them by mutagenesis/recombination-essential methods for today's study of functional genomics, gene expression, protein structure-function relationships, protein engineering, and molecular evolution.

07. Zustand: Wie neu. 1997. 490 S., zahlr. Abb. u. Tab. Contains more than 100 step-by-step protocols supported by troubleshooting tips, alternative procedures, and informative explanations of why certain steps are done to guarantee a greater chance for the successful reproduction of an experiment. Sprache: Deutsch.

Totowa NJ 2002. xiv,439 p. bound (Methods in Molecular Biology vol.192; $ 140.-).