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Recombinant DNA. : Part E /
Recombinant DNA methods are powerful, revolutionary techniques for at least two reasons. First, they allow the isolation of single genes in large amounts from a pool of thousands or millions of genes. Second, the isolated genes or their regulatory regions can be modified at will and re-introduced in...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
San Diego :
Academic Press,
1987.
|
| Colección: | Methods in enzymology ;
v. 154. |
| Temas: | |
| Acceso en línea: | Texto completo Texto completo |
MARC
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| 020 | |a 9780121820558 |q (electronic bk.) | ||
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| 050 | 4 | |a QP601 | |
| 060 | 4 | |a W1 |b ME321 v.154 1987 | |
| 082 | 0 | 4 | |a 574.19 |
| 245 | 0 | 0 | |a Recombinant DNA. : |b Part E / |c edited by Ray Wu [and] Lawrence Grossman. |
| 260 | |a San Diego : |b Academic Press, |c 1987. | ||
| 300 | |a 1 online resource (xxviii, 576 pages) : |b illustrations. | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Methods in enzymology ; |v v. 154 | |
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record. | |
| 520 | |a Recombinant DNA methods are powerful, revolutionary techniques for at least two reasons. First, they allow the isolation of single genes in large amounts from a pool of thousands or millions of genes. Second, the isolated genes or their regulatory regions can be modified at will and re-introduced into cells for expression at the RNA or protein levels. These attributes help to solve complex biological problems and to produce new and better products in the areas of health, agriculture and industry. Both volume 154 and 155 include the descriptions of several useful new restriction enzymes and rapid methods for DNA sequence analysis, along with a number of other useful methods. | ||
| 505 | 0 | |a Section I. Methods for cloning cDNA -- Section II. Identification of cloned genes and mapping of genes -- Section III. Chemical synthesis and analysis of oligodeoxynucleotides -- Section IV. Site-specific mutagenesis and protein engineering. | |
| 650 | 0 | |a Recombinant DNA. | |
| 650 | 2 | |a DNA, Recombinant |0 (DNLM)D004274 | |
| 650 | 6 | |a ADN recombinant. |0 (CaQQLa)201-0024828 | |
| 650 | 7 | |a Enzymes. |2 eclas | |
| 650 | 7 | |a Biochimie. |2 eclas | |
| 650 | 7 | |a Recombinant DNA |2 fast |0 (OCoLC)fst01091466 | |
| 650 | 7 | |a ADN recombin�e. |2 fmesh | |
| 650 | 7 | |a ADN recombin�e. |2 ram | |
| 700 | 1 | |a Grossman, Lawrence, |d 1924-2006. | |
| 700 | 1 | |a Wu, Ray. | |
| 776 | 0 | 8 | |i Print version: |t Recombinant DNA. |d San Diego : Academic Press, 1987 |z 0121820556 |w (DLC) 54009110 |w (OCoLC)17315745 |
| 830 | 0 | |a Methods in enzymology ; |v v. 154. | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780121820558 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/00766879/154 |z Texto completo |