Office of Academic Resources
Chulalongkorn University
Chulalongkorn University

Home / Help

TitleMeiosis [electronic resource] : Volume 1, Molecular and Genetic Methods
Author edited by Scott Keeney
ImprintTotowa, NJ : Humana Press, 2009
Connect tohttp://dx.doi.org/10.1007/978-1-59745-527-5
Descript XII, 372 p. 63 illus. online resource

SUMMARY

The unique chromosome dynamics of meiosis have fascinated scientists for well over a century, but in recent years there has been a proliferation of new data concerning the pairing, recombination, and segregation of chromosomes. In Meiosis, expert researchers explore recent advances in three main areas: quantitative genetic methods for analysis of homologous recombination and chromosome pairing, development of direct physical assays for DNA intermediates and products of recombination, and cytological methods for characterizing chromosome behaviors and the patterns by which specific proteins associate with meiotic chromosomes. Meiosis: Volume 1, Molecular and Genetic Methods details methods for culturing and manipulating commonly used model organisms and protocols for detecting and quantifying meiotic recombination events through genetic and physical analysis of DNA-DNA or Protein-DNA interactions. Methods are provided for studies in yeasts, plants, and animals, including mouse and human. Composed in the highly successful Methods in Molecular Biology(tm) series format, each chapter contains a brief introduction, step-by-step methods, a list of necessary materials, and a Notes section which shares tips on troubleshooting and avoiding known pitfalls. Comprehensive and cutting-edge, Meiosis: Volume 1, Molecular and Genetic Methods is an essential guidebook, providing up-to-date and critical new protocols for the study of meiotic chromosome dynamics


CONTENT

Genetic Methods for Studying Meiotic Recombination and Chromosome Dynamics -- Interaction of Genetic and Environmental Factors in Saccharomyces cerevisiae Meiosis: The Devil is in the Details -- Optimizing Sporulation Conditions for Different Saccharomyces cerevisiae Strain Backgrounds -- Modulating and Targeting Meiotic Double-Strand Breaks in Saccharomyces cerevisiae -- Methods for Analysis of Crossover Interference in Saccharomyces cerevisiae -- Measurement of Spatial Proximity and Accessibility of Chromosomal Loci in Saccharomyces cerevisiae Using Cre?/loxP Site-Specific Recombination -- Genetic Analysis of Meiotic Recombination in Schizosaccharomyces pombe -- Analysis of Meiotic Recombination in Caenorhabditis elegans -- Visual Markers for Detecting Gene Conversion Directly in the Gametes of Arabidopsis thaliana -- Molecular Analysis of Recombination and Protein-DNA Interactions During Meiosis -- Gel Electrophoresis Assays for Analyzing DNA Double-Strand Breaks in Saccharomyces cerevisiae at Various Spatial Resolutions -- Genome-Wide Mapping of Meiotic DNA Double-Strand Breaks in Saccharomyces cerevisiae -- Detection of Meiotic DNA Breaks in Mouse Testicular Germ Cells -- End-Labeling and Analysis of Spo11-Oligonucleotide Complexes in Saccharomyces cerevisiae -- Detection of SPO11-Oligonucleotide Complexes from Mouse Testes -- Stabilization and Electrophoretic Analysis of Meiotic Recombination Intermediates in Saccharomyces cerevisiae -- Using Schizosaccharomyces pombe Meiosis to Analyze DNA Recombination Intermediates -- Analysis of Chromatin Structure at Meiotic DSB Sites in Yeasts -- Analysis of Protein–DNA Interactions During Meiosis by Quantitative Chromatin Immunoprecipitation (qChIP) -- Genome-Wide High-Resolution Chromatin Immunoprecipitation of Meiotic Chromosomal Proteins in Saccharomyces cerevisiae -- Parallel Detection of Crossovers and Noncrossovers in Mouse Germ Cells -- Analysis of Meiotic Recombination Products from Human Sperm


Life sciences Cell biology Microbiology Life Sciences Cell Biology Microbiology Eukaryotic Microbiology



Location



Office of Academic Resources, Chulalongkorn University, Phayathai Rd. Pathumwan Bangkok 10330 Thailand

Contact Us

Tel. 0-2218-2929,
0-2218-2927 (Library Service)
0-2218-2903 (Administrative Division)
Fax. 0-2215-3617, 0-2218-2907

Social Network

  line

facebook   instragram