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Integrated Genomics: A Discovery-Based Laboratory Course introduces the excitement of discovery to the basic molecular biology laboratory. Utilizing up-to-date molecular biology protocols… mais…

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Integrated Genomics: A Discovery-Based Laboratory Course
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Integrated Genomics - Caldwell, Guy A. Williams, Shelli N. Caldwell, Kim A.
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Caldwell, Guy A. Williams, Shelli N. Caldwell, Kim A.:
Integrated Genomics - primeira edição

2006

ISBN: 9780470095027

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Integrated Genomics - Livro de bolso

ISBN: 9780470095027

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Integrated Genomics ? A Discovery?Based Laboratory Course - Guy A. Caldwell; Shelli N. Williams; Kim A. Caldwell
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Guy A. Caldwell; Shelli N. Williams; Kim A. Caldwell:
Integrated Genomics ? A Discovery?Based Laboratory Course - Livro de bolso

2006, ISBN: 9780470095027

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Integrated Genomics
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9780470095027


Diese spannende, gut nachvollziehbare Einführung in das moderne Gebiet der Genomforschung ist eine gelungene Mischung ais methogologischen Informationen zur Molekularbiologie und Arbeitsanleitungen zur sinnvollen Benutzung online verfügbarer Datenbanken.

Dados detalhados do livro - Integrated Genomics


EAN (ISBN-13): 9780470095027
ISBN (ISBN-10): 0470095024
Livro de capa dura
Livro de bolso
Ano de publicação: 2006
Editor/Editora: John Wiley & Sons
225 Páginas
Peso: 0,576 kg
Língua: eng/Englisch

Livro na base de dados desde 2008-06-12T18:22:41-03:00 (Sao Paulo)
Página de detalhes modificada pela última vez em 2023-04-13T07:36:07-03:00 (Sao Paulo)
Número ISBN/EAN: 9780470095027

Número ISBN - Ortografia alternativa:
0-470-09502-4, 978-0-470-09502-7
Ortografia alternativa e termos de pesquisa relacionados:
Autor do livro: shelli, williams, guy, kim, john caldwell
Título do livro: integrated genomics discovery based laboratory course

Dados da editora

Autor: Guy Caldwell; Shelli Williams; Kim Caldwell
Título: Integrated Genomics - A Discovery-Based Laboratory Course
Editora: Wiley; John Wiley & Sons
248 Páginas
Ano de publicação: 2006-07-28
Peso: 0,719 kg
Língua: Inglês
79,90 € (DE)
Not available (reason unspecified)
216mm x 279mm x 15mm

BC; Hardcover, Softcover / Biologie/Genetik, Gentechnik; Genetik (nicht-medizinisch); Biowissenschaften; Genetics; Genetik; Genomics; Life Sciences; Genetik; BB

Preface. Author biographies. Acknowledgments. List of figures. 1 Introduction to basic laboratory genetics. 1.1 Transferring and handling C. elegans. 1.2 Introduction to laboratory genetics. 2 Gene expression analysis using transgenic animals. 2.1 Transgenic gene expression analysis in C. elegans: lacZ staining. 2.2 Transgenic gene expression analysis in C. elegans: GFP analysis. 3 Creation and testing of transgenic yeast for use in protein-protein interaction screening. 3.1 Small-scale transformation of S. cerevisiae. 3.2 Transformation of S. cerevisiae to test for non-specific interaction. 3.3 Assaying for protein-protein interaction by reporter gene expression. 4 Yeast two-hybrid screening. 4.1 Protein-protein interaction screening of a C. elegans cDNA library. 4.2 Assaying for protein-protein interaction by reporter gene expression. 5 Isolation and identification of interacting proteins. 5.1 Preparation of electrocompetent E. coli. 5.2 Isolation of DNA from yeast and electroporation of E. coli. 5.3 Small-scale isolation of plasmid DNA from E. coli: the mini-prep. 5.4 Sequencing of two-hybrid library plasmid DNA vectors. 6 Using bioinformatics in modern science. 6.1 DNA sequence chromatogram. 6.2 BLASTing your sequence. 6.3 Evaluating sequence results and choosing an RNAi target. 6.4 Bioinformatics practice questions. 7 Generation of an RNAi vector. 7.1 Small-scale isolation of genomic DNA from C. elegans. 7.2 PCR amplification of target gene sequence from C. elegans genomic DNA. 7.3 Preparations for cloning to generate RNAi vector. 7.3.1 Agarose gel electrophoresis. 7.3.2 Removal of dNTPs from PCR reaction. 7.3.3 Restriction enzyme digestion of PCR product and C. elegans RNAi vector. 7.4 Gel purification of DNA and ligation of vector and PCR-amplified DNA. 7.4.1 Preparative agarose gel electrophoresis. 7.4.2 Gel purification of DNA from agarose gel. 7.4.3 Ligation of vector and PCR-amplified DNA. 7.5 Transformation of ligation reactions. 7.6 PCR screening of transformation colonies. 7.7 Small-scale isolation of plasmid DNA from E. coli: the mini-prep. 7.8 Verifying successful ligation by restriction digestion. 8 RNA-mediated interference by bacterial feeding. 8.1 Preparation of RNAi-feeding bacteria for transformation. 8.2 Media preparation for RNAi feeding. 8.3 Transformation of RNAi-feeding strain HT115(DE3). 8.4 RNA interference by bacterial feeding of C. elegans. 8.5 Analyzing effects of dsRNAi. 8.5.1 Assaying for sterility (Ste) or embryonic lethality (Emb). 8.5.2 Assaying for growth effect. 8.5.3 Assaying for morphological effects. 8.5.4 Assaying for general neuromuscular effects. 8.5.5 Assaying for specific neuronal effects. 8.5.6 Assaying for dauer formation. Appendix I Recombinational cloning. AI.1 Isolation of genomic DNA from C. elegans. AI.2 PCR amplification of target gene sequence from C. elegans genomic DNA. AI.3 Agarose gel electrophoresis and clean-up of PCR reaction. AI.4 Entry vector cloning. AI.5 Small-scale isolation of plasmid DNA from E. coli: the mini-prep. AI.6 Destination vector cloning. AI.7 Small-scale isolation of plasmid DNA from E. coli: the mini-prep. Appendix II Recipes and media preparation. Solution recipes. Media preparation. Appendix III Sterile techniques and worm protocols. Sterile techniques. Worm protocols. Appendix IV Mutant C. elegans phenotypes. Appendix V Vector maps. Subject index.

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