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Titlebook: Genetic Recombination; Reviews and Protocol Alan S. Waldman Book 2004 Humana Press 2004

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发表于 2025-3-21 17:04:10 | 显示全部楼层 |阅读模式
书目名称Genetic Recombination
副标题Reviews and Protocol
编辑Alan S. Waldman
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Genetic Recombination; Reviews and Protocol Alan S. Waldman Book 2004 Humana Press 2004
描述Genetic recombination, in the broadest sense, can be defined as any process in which DNA sequences interact and undergo a transfer of information, producing new “recombinant” sequences that contain information from each of the original molecules. All organisms have the ability to carry out recombination, and this striking universality speaks to the essential role recombination plays in a variety of biological processes fundamentally important to the maintenance of life. Such processes include DNA repair, regulation of gene expression, disease etiology, meiotic chromosome segregation, and evolution. One important aspect of recombination is that it typically occurs only between sequences that display a high degree of sequence identity. The stringent requirement for homology helps to ensure that, under normal circumstances, a cell is protected from deleterious rearrangements since a swap of genetic information between two nearly identical sequences is not expected to dramatically alter a genome. Recombination between dissimilar sequences, which does happen on occasion, may have such harmful consequences as chromosomal translocations, deletions, or inversions. For many organisms, it is
出版日期Book 2004
版次1
doihttps://doi.org/10.1385/1592597610
isbn_softcover978-1-61737-442-5
isbn_ebook978-1-59259-761-1Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2004
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Detecting Carcinogens With the Yeast DEL Assayaddition to the arsenal of predictive tests for genotoxicity and carcinogenicity. This chapter provides an in-depth description of materials and methods for the yeast DEL assay from a user’s prospective and should allow the assay to be successfully deployed in any laboratory with basic microbiological capability and minimal user training.
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Chromatin Immunoprecipitation to Investigate Protein-DNA Interactions During Genetic Recombination the protein. Polymerase chain reaction (PCR) is then used to determine the relative amounts of DNA associated with the protein of interest throughout the recombination event. This in vivo chemical crosslinking technique can be used to localize proteins to both double-strand breaks and recombination intermediates.
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Barriers to Change and Hope for the Future,cribe a protocol for increasing the frequency of TNE in the true yeast, ., through the use of nonspecific, carrier oligonucleotides. These molecules, when added to the reaction, increase the TNE frequency up to 25-fold in some cases, perhaps by providing a molecular trap to bind factors, which may inactivate the specific targeting oligos.
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https://doi.org/10.1007/978-94-6351-029-5ealing of partially complementary oligonucleotides; and (2) a true recombination intermediate structure formed by RecA protein-mediated strand exchange. The use of these substrates in assays designed to detect Holliday junction branch migration and resolution activities is described.
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DNA Fragment Transplacement in ,tions of transformation efficiency, length of homology, and alternative target site configuration were assessed. This analysis indicates that several genetic parameters are important for optimizing the efficiency of gene transplacement.
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