Advanced Bacterial Genetics: Use of Transposons and Phage for Genomic Engineering: Methods in Enzymology, cartea 421
Kelly T Hughesen Limba Engleză Hardback – 15 mar 2007
Din seria Methods in Enzymology
- 32% Preț: 801.30 lei
- 23% Preț: 452.05 lei
- 23% Preț: 451.31 lei
- 23% Preț: 430.98 lei
- 23% Preț: 439.12 lei
- 23% Preț: 442.31 lei
- 23% Preț: 436.20 lei
- 5% Preț: 545.92 lei
- 23% Preț: 441.58 lei
- 23% Preț: 437.23 lei
- 23% Preț: 427.08 lei
- 23% Preț: 436.94 lei
- 23% Preț: 450.28 lei
- 23% Preț: 450.74 lei
- 23% Preț: 447.41 lei
- 23% Preț: 441.46 lei
- 23% Preț: 444.33 lei
- 5% Preț: 553.96 lei
- 23% Preț: 441.58 lei
- 23% Preț: 454.95 lei
- 23% Preț: 432.59 lei
- 23% Preț: 438.41 lei
- 23% Preț: 449.87 lei
- 23% Preț: 441.29 lei
- 23% Preț: 436.82 lei
- 23% Preț: 436.36 lei
- 23% Preț: 433.61 lei
- 23% Preț: 441.29 lei
- 23% Preț: 439.56 lei
- 23% Preț: 438.54 lei
- 23% Preț: 449.70 lei
- 23% Preț: 432.01 lei
- 23% Preț: 439.12 lei
- 23% Preț: 457.42 lei
- 23% Preț: 442.31 lei
- 23% Preț: 444.50 lei
- 23% Preț: 449.87 lei
- 23% Preț: 448.27 lei
- 23% Preț: 438.41 lei
- 5% Preț: 550.03 lei
- 23% Preț: 438.54 lei
- 23% Preț: 444.20 lei
- 23% Preț: 433.03 lei
- 23% Preț: 441.29 lei
- 23% Preț: 440.14 lei
- 23% Preț: 446.84 lei
- 23% Preț: 445.94 lei
- 23% Preț: 446.67 lei
- 23% Preț: 442.03 lei
Preț: 1212.33 lei
Preț vechi: 1660.73 lei
-27% Nou
Puncte Express: 1818
Preț estimativ în valută:
232.02€ • 241.00$ • 192.72£
232.02€ • 241.00$ • 192.72£
Carte tipărită la comandă
Livrare economică 03-17 februarie 25
Preluare comenzi: 021 569.72.76
Specificații
ISBN-13: 9780123737496
ISBN-10: 0123737494
Pagini: 320
Ilustrații: Illustrated
Dimensiuni: 152 x 229 x 24 mm
Greutate: 0.7 kg
Editura: ELSEVIER SCIENCE
Seria Methods in Enzymology
ISBN-10: 0123737494
Pagini: 320
Ilustrații: Illustrated
Dimensiuni: 152 x 229 x 24 mm
Greutate: 0.7 kg
Editura: ELSEVIER SCIENCE
Seria Methods in Enzymology
Public țintă
Biochemists, geneticists, and molecular biologists.Cuprins
Section I. Strain Collections and Genetic Nomenclature.
Chapter 1. Strain Collections and Genetic Nomenclature.
Section II. Transposons.
Chapter 2: Use of Antibiotic Resistant Transposons for Mutagenesis.
Chapter 3: In vivo Mutagenesis Using EZ-Tn5TM.
Chapter 4: Identification of essential genes in bacteria.
Chapter 5: Isolation and use of linked transposons.
Chapter 6: Localized mutagenesis.
Chapter 7: Generation of deletions and duplications using transposons as portable regions of homology with emphasis on Mud and Tn10 transposons.
Chapter 8: Target-Directed Proteolysis in vivo.
Chapter 9: Sets of transposon generated sequence-tagged mutants for structure-function analysis and engineering.
Chapter 10: Using Genomic Microarrays to Study Insertional/Transposon Mutant Libraries.
Chapter 11: Screening Transposon Mutant Libraries Using Full-Genome Oligonucleotide Microarrays.
Chapter 12: Creating recombination-activated genes and sequence-defined mutant libraries using transposons
Chapter 13: Use of transposons to study genetic regulation fusions.
Chapter 14: Genomic screening for regulatory genes using the T-POP transposon.
Section III. Phage.
Chapter 15: Recombineering: in vivo genetic engineering in E. coli, S. enterica and beyond.
Chapter 16: Ć-Red Genetic Engineering in Salmonella enterica serovar Typhimurium.
Chapter 17: Integrase.
Chapter 18: Challenge phage.
Chapter 19: MudP22.
Chapter 20: Phage metagenomics.
Chapter 1. Strain Collections and Genetic Nomenclature.
Section II. Transposons.
Chapter 2: Use of Antibiotic Resistant Transposons for Mutagenesis.
Chapter 3: In vivo Mutagenesis Using EZ-Tn5TM.
Chapter 4: Identification of essential genes in bacteria.
Chapter 5: Isolation and use of linked transposons.
Chapter 6: Localized mutagenesis.
Chapter 7: Generation of deletions and duplications using transposons as portable regions of homology with emphasis on Mud and Tn10 transposons.
Chapter 8: Target-Directed Proteolysis in vivo.
Chapter 9: Sets of transposon generated sequence-tagged mutants for structure-function analysis and engineering.
Chapter 10: Using Genomic Microarrays to Study Insertional/Transposon Mutant Libraries.
Chapter 11: Screening Transposon Mutant Libraries Using Full-Genome Oligonucleotide Microarrays.
Chapter 12: Creating recombination-activated genes and sequence-defined mutant libraries using transposons
Chapter 13: Use of transposons to study genetic regulation fusions.
Chapter 14: Genomic screening for regulatory genes using the T-POP transposon.
Section III. Phage.
Chapter 15: Recombineering: in vivo genetic engineering in E. coli, S. enterica and beyond.
Chapter 16: Ć-Red Genetic Engineering in Salmonella enterica serovar Typhimurium.
Chapter 17: Integrase.
Chapter 18: Challenge phage.
Chapter 19: MudP22.
Chapter 20: Phage metagenomics.