Richard J. Reece

Analysis of Genes and Genomes

• Broschiertes Buch

Produktbeschreibung

This beautifully illustrated textbook provides a clear guide to the tools and techniques of genetic engineering, gene cloning and molecular biology. All aspects of genetic engineering in the post-genomic era are covered, beginning with the basics of DNA structure and DNA metabolism. Using an example-driven approach, the fundamentals of creating mutations in DNA, cloning in bacteria, yeast, plants and animals are all clearly presented.

Strong emphasis is placed on the latest, post genomic technologies including DNA macro and microarrays, genome-wide two hybrid analysis, proteomics and bioinformatics.
_ A modern post-genome era introduction to key techniques used in genetic engineering.
_ An example driven past-to-present approach to allow the experiments of today to be placed in an historical context
_ The book is beautifully illustrated in full-colour throughout.
_ Associated website including updates, additional content and illusions

Produktdetails

• Verlag: Wiley & Sons
• 1. Auflage
• Seitenzahl: 496
• Erscheinungstermin: 16. Januar 2004
• Englisch
• Abmessung: 246mm x 189mm x 26mm
• Gewicht: 1195g
• ISBN-13: 9780470843802
• ISBN-10: 0470843802
• Artikelnr.: 12355875

Autorenporträt

Richard J. Reece is the author of Analysis of Genes and Genomes, published by Wiley.

Inhaltsangabe

Preface. Acknowledgements. Dedication. 1. DNA: structure and function. 1.1
Nucleic acid is the material of heredity. 1.2 Structure of nucleic acids.
1.3 The double helix. 1.4 Reversible denaturing of DNA. 1.5 Structure of
DNA in the cell. 1.6 The eukaryotic nucleosome. 1.7 The replication of DNA.
1.8 DNA polymerases. 1.9 The replication process. 1.10 Recombination. 1.11
Genes and genomes. 1.12 Genes within a genome. 1.13 Transcription. 1.14 RNA
processing. 1.15 Translation. 2. Basic techniques in gene analysis. 2.1
Restriction enzymes. 2.2 Joining DNA molecules. 2.3 The basics of cloning.
2.4 Bacterial transformation. 2.5 Gel electrophoresis. 2.6 Nucleic acid
blotting. 2.7 DNA purification. 3. Vectors. 3.1 Plasmids. 3.2 Selectable
markers. 3.3 l Vectors. 3.4 Cosmid vectors. 3.5 M1 3 vectors. 3.6
Phagemids. 3.7 Artificial chromosomes. 4. Polymerase chain reaction. 4.1
PCR reaction conditions. 4.2 Thermostable DNA polymerases. 4.3 Template
DNA. 4.4 Oligonucleotide primers. 4.5 Primer mismatches. 4.6 PCR in the
diagnosis of genetic disease. 4.7 Cloning PCR products. 4.8 RT-PCR. 4.9
Real-time PCR. 4.10 Applications of PCR. 5. Cloning a gene. 5.1 Genomic
libraries. 5.2 cDNA libraries. 5.3 Directional cDNA cloning. 5.4 PCR-based
libraries. 5.5 Subtraction libraries. 5.6 Library construction in the
post-genome era. 6. Gene identification. 6.1 Screening by nucleic acid
hybridization. 6.2 Immunoscreening. 6.3 Screening by function. 6.4
Screening by interaction. 6.5 Phage display. 6.6 Two-hybrid screening. 6.7
Other interaction screens - variations on a theme. 7. Creating mutations.
7.1 Creating specific mutations. 7.2 Primer extension mutagenesis. 7.3
Strand selection methods. 7.4 Cassette mutagenesis. 7.5 PCR-based
mutagenesis. 7.6 QuikChange(r) mutagenesis. 7.7 Creating random mutations
in specific genes. 7.8 Protein engineering. 8. Protein production and
purification. 8.1 Expression in E. coli. 8.2 Expression in yeast. 8.3
Expression in insect cells. 8.4 Expression in higher eukaryotic cells. 8.5
Protein purification. 9. Genome sequencing projects. 9.1 Genomic mapping.
9.2 Genetic mapping. 9.3 Physical mapping. 9.4 Nucleotide sequencing. 9.5
Genome sequencing. 9.6 The Human Genome Project. 9.7 Finding genes. 9.8
Gene assignment. 9.9 Bioinformatics. 10. Post-genome analysis. 10.1 Global
changes in gene expression. 10.2 Protein function on a genome-wide scale.
10.3 Knock-out analysis. 10.4 Antisense and RNA interference (RNAi). 10.5
Genome-wide two-hybrid screens. 10.6 Protein-detection arrays. 10.7
Structural genomics. 11. Engineering plants. 11.1 Cloning in plants. 11.2
Commercial exploitation of plant transgenics. 11.3 Ethics of genetically
engineered crops. 12. Engineering animal cells. 12.1 Cell culture. 12.2
Transfection of animal cells. 12.3 Viruses as vectors. 12.4 Selectable
markers and gene amplification in animal cells. 12.5 Expressing genes in
animal cells. 13. Engineering animals. 13.1 Pronuclear injection. 13.2
Embryonic stem cells. 13.3 Nuclear transfer. 13.4 Gene therapy. 13.5
Examples and potential of gene therapy. Glossary. Appendices. Nobel prize
winners. References. Index.

Rezensionen

"It could be an excellent supporting book to go along with a more general text in a course covering molecular biology." (Biochemistry and Molecular Education, July/ August 2004)

"...the list of relevant Nobel laureates at the end will be useful and was a delight..." (Heredity, Vol. 94, 2005)

"...the full range of topics one would wish to see in such a book are covered...I certainly welcome the book..." (Genetical Research, Vol.84, 2004)

" ... invaluable to those looking to better understand the complexities and capabilities of these important new technologies." (Thaiszia Journal of Botany, Vol. 15; 173-185, 2005)