The first libraries of complementary DNA (cDNA) clones were con structed in the mid-to-late 1970s using RNA-dependent DNA polymerase (reverse transcriptase) to convert poly A* mRNA into double-stranded cDNA suitable for insertion into prokaryotic vectors. Since then cDNA technology has become a fundamental tool for the molecular biologist and at the same time some very significant advances have occurred in the methods for con structing and screening cDNA libraries. It is not the aim of cDNA Library Protocols to give a comprehensive review of all cDNA library-based methodologies; instead we present a series of up-to-date protocols that together should give a good grounding of proce dures associated with the construction and use of cDNA libraries. In deciding what to include, we endeavored to combine up-to-date versions of some of the most widely used protocols with some very usefiil newer techniques. cDNA Library Protocols should therefore be especially useful to the investigator who is new to the use of cDNA libraries, but should also be of value to the more experienced worker. Chapters 1—5 concentrate on cDNA library construction and manipula tion, Chapters 6 and 7 describe means of cloning difficult-to-obtain ends of cDNAs, Chapters 8-18 give various approaches to the screening of cDNA libraries, and the remaining chapters present methods of analysis of cDNA clones including details of how to analyze cDNA sequence data and how to make use of the wealth of cDNA data emerging from the human genome project.
Le informazioni nella sezione "Riassunto" possono far riferimento a edizioni diverse di questo titolo.
This is a good overview of the essentials for preparing a cDNA library, for both the novice and the expert...the book is a true laboratory manual for the experimental scientist. It Should represent a useful and up-to-date addition for any lab that, for whatever reason, needs to generate its own libraries.-Hoffman-LaRoche, Inc.
"...their fine layout and ease of use suggest that the lab copy won't stay on the bookshelf for long."-SGM Quarterly
cDNA Library Construction from Small Amounts of RNA Using Paramagnetic Beads and PCR Kris N. Lambert and Valerie M. Williamson Increasing the Average Abundance of Low-Abundance cDNAs by Ordered Subdivision of cDNA Populations David R. Sibson and Michael P. Starkey Isolation of Messenger RNA from Plant Tissues Alison Dunn cDNA Library Construction for the Lambda ZAP®-Based Vectors Marjory A. Snead, Michelle A. Alting-Mees, and Jay M. Short Clone Excision Methods for the Lambda ZAP®-Based Vectors Marjory A. Snead, Michelle A. Alting-Mees, and Jay M. Short Using Rapid Amplification of cDNA Ends (RACE) to Obtain Full-Length cDNAs Yue Zhang and Michael A. Frohman Inverse PCR Approach to Cloning cDNA Ends Sheng-He Huang Cloning Gene Family Members Using the Polymerase Chain Reaction with Degenerate Oligonucleotide Primers Gregory M. Preston Subtractive Hybridization for the Isolation of Differentially Expressed Genes Using Magnetic Beads Hans-Christian Aasheim, Ton Logtenberg, and Frank Larsen Preparation of Competent Cells for High-Efficiency Plasmid Transformation of Escherichia coli Yasuhiko Nakata, Xiaoren Tang, and Kazunari K. Yokoyama The Tetramethylammonium Chloride (TMAC) Method for Screening cDNA Libraries with Highly Degenerate Oligonucleotide Probes Obtained by Reverse Translation of Amino Acid Sequences Bent Honoré and Peder Madsen Screening cDNA Libraries by Hybridization with Double-Stranded DNA Probes and Oligonucleotides Caroline A. Austin Immunological Screening of l-Phage cDNA Expression Libraries Helen C. Hurst Cloning Sequence-Specific DNA-Binding Factors from cDNA Expression Libraries Using Oligonucleotide Binding Site Probes Ian G. Cowell Protein Interaction Cloning by Far-Western Screening of l-Phage cDNA ExpressionLibraries Shinichi Takayama and John C. Reed Yeast Two-Hybrid Library Screening Ian G. Cowell Signal Sequence Trap: Expression Cloning Method for Secreted Proteins and Type 1 Membrane Proteins Kei Tashiro, Toru Nakano, and Tasuku Honjo Isolation of Genetic Suppressor Elements (GSEs) from Random Fragment cDNA Libraries in Retroviral Vectors Andrei V. Gudkov and Igor B. Roninson Expression and Preparation of Fusion Proteins from Recombinant lgt11 Phages Sheng-He Huang and Ambrose Jong Computer Analysis of Cloned Sequences Paul R. Caron The TIGR Human cDNA Database Ewen F. Kirkness and Anthony R. Kerlavage Searching the dbEST Database Patricia Rodriguez Tomé Reference cDNA Library Facilities Available from European Sources Michael P. Starkey, Yagnesh Umrania, Christopher R. Mundy, and Martin J. Bishop Index
Le informazioni nella sezione "Su questo libro" possono far riferimento a edizioni diverse di questo titolo.
Da: Red's Corner LLC, Tucker, GA, U.S.A.
Paperback. Condizione: Fine. All orders ship by next business day! This is a used book. Grade 4 out of 5 points. Book may have wear due to handling. Has no markings on pages. May not include extra materials like access codes, CDs, accessories, etc. We are a small company and very thankful for your business! Softcover reprint of the original 1st ed. Codice articolo 4CNO3I002MWM
Quantità: 1 disponibili
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The first libraries of complementary DNA (cDNA) clones were con structed in the mid-to-late 1970s using RNA-dependent DNA polymerase (reverse transcriptase) to convert poly A\* mRNA into double-stranded cDNA suitable for insertion into prokaryotic vectors. Since then cDNA technology has become a fundamental tool for the molecular biologist and at the same time some very significant advances have occurred in the methods for con structing and screening cDNA libraries. It is not the aim of cDNA Library Protocols to give a comprehensive review of all cDNA library-based methodologies; instead we present a series of up-to-date protocols that together should give a good grounding of proce dures associated with the construction and use of cDNA libraries. In deciding what to include, we endeavored to combine up-to-date versions of some of the most widely used protocols with some very usefiil newer techniques. cDNA Library Protocols should therefore be especially useful to the investigator who is new to the use of cDNA libraries, but should also be of value to the more experienced worker. Chapters 1-5 concentrate on cDNA library construction and manipula tion, Chapters 6 and 7 describe means of cloning difficult-to-obtain ends of cDNAs, Chapters 8-18 give various approaches to the screening of cDNA libraries, and the remaining chapters present methods of analysis of cDNA clones including details of how to analyze cDNA sequence data and how to make use of the wealth of cDNA data emerging from the human genome project. 332 pp. Englisch. Codice articolo 9781489940506
Quantità: 2 disponibili
Da: Brook Bookstore On Demand, Napoli, NA, Italia
Condizione: new. Questo è un articolo print on demand. Codice articolo L4NB36PLKR
Quantità: Più di 20 disponibili
Da: Ria Christie Collections, Uxbridge, Regno Unito
Condizione: New. In. Codice articolo ria9781489940506_new
Quantità: Più di 20 disponibili
Quantità: Più di 20 disponibili
Da: Books Puddle, New York, NY, U.S.A.
Condizione: New. pp. 332. Codice articolo 26134210241
Quantità: 4 disponibili
Da: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irlanda
Condizione: New. Editor(s): Cowell, Ian G.; Austin, Caroline A. Series: Methods in Molecular Biology. Num Pages: 321 pages, 28 black & white illustrations, biography. BIC Classification: MJCM; PSF. Category: (P) Professional & Vocational. Dimension: 230 x 153 x 18. Weight in Grams: 486. . 2013. Softcover reprint of the original 1st ed. 1997. Paperback. . . . . Codice articolo V9781489940506
Quantità: 15 disponibili
Da: preigu, Osnabrück, Germania
Taschenbuch. Condizione: Neu. cDNA Library Protocols | Ian G. Cowell (u. a.) | Taschenbuch | x | Englisch | 2013 | Humana | EAN 9781489940506 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. Codice articolo 105124209
Quantità: 5 disponibili
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germania
Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The first libraries of complementary DNA (cDNA) clones were con structed in the mid-to-late 1970s using RNA-dependent DNA polymerase (reverse transcriptase) to convert poly A\* mRNA into double-stranded cDNA suitable for insertion into prokaryotic vectors. Since then cDNA technology has become a fundamental tool for the molecular biologist and at the same time some very significant advances have occurred in the methods for con structing and screening cDNA libraries. It is not the aim of cDNA Library Protocols to give a comprehensive review of all cDNA library-based methodologies; instead we present a series of up-to-date protocols that together should give a good grounding of proce dures associated with the construction and use of cDNA libraries. In deciding what to include, we endeavored to combine up-to-date versions of some of the most widely used protocols with some very usefiil newer techniques. cDNA Library Protocols should therefore be especially useful to the investigator who is new to the use of cDNA libraries, but should also be of value to the more experienced worker. Chapters 1¿5 concentrate on cDNA library construction and manipula tion, Chapters 6 and 7 describe means of cloning difficult-to-obtain ends of cDNAs, Chapters 8-18 give various approaches to the screening of cDNA libraries, and the remaining chapters present methods of analysis of cDNA clones including details of how to analyze cDNA sequence data and how to make use of the wealth of cDNA data emerging from the human genome project.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 332 pp. Englisch. Codice articolo 9781489940506
Quantità: 1 disponibili
Da: Majestic Books, Hounslow, Regno Unito
Condizione: New. Print on Demand pp. 332 23:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on White w/Gloss Lam. Codice articolo 126377246
Quantità: 4 disponibili