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Titlebook: Gene Knockout Protocols; Wolfgang Wurst,Ralf Kühn Book 2009Latest edition Humana Press 2009 DNA.ES cells.Gene modification.Genetically eng

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发表于 2025-3-21 18:02:08 | 显示全部楼层 |阅读模式
书目名称Gene Knockout Protocols
编辑Wolfgang Wurst,Ralf Kühn
视频video
概述Comprehensive guide to all techniques required for the generation of classical and conditional knockout mouse strains.Includes techniques for ES cell establishment, ES cell in vitro differentatio, and
丛书名称Methods in Molecular Biology
图书封面Titlebook: Gene Knockout Protocols;  Wolfgang Wurst,Ralf Kühn Book 2009Latest edition Humana Press 2009 DNA.ES cells.Gene modification.Genetically eng
描述Following the completion of the mouse and human genome sequences, a major challengeisthefunctionalcharacterizationofeverymammaliangeneandthedeciph- ing of their molecular interaction network. The mouse offers many advantages for the use of genetics to study human biology and disease, unmatched among other m- mals. Its development, body plan, physiology, behavior, and diseases have much in common, based on the fact that 99% of the human genes have a mouse ortholog. The investigation of gene function using mouse models is based on many years of tech- logical development. In the two decades since gene targeting in murine embryonic stem (ES) cells was first described by Mario Capecchi and colleagues, more than 3000 predesigned mouse mutants have been developed. To date, a variety of mouse mutagenesis techniques, either gene- or phenotype-driven, are used as systematic approaches. The availability of the genome sequence supports gene-driven approaches such as gene-trap and targeted mutagenesis in ES cells, allowing efficient and precise gene disruption. In combination with the use of site-specific DNA recombinases, in particular the Cre/loxP system, gene disruptioncan be directed to spe
出版日期Book 2009Latest edition
关键词DNA; ES cells; Gene modification; Genetically engineered mice; Mouse genome; Mutagenesis techniques; Mutan
版次2
doihttps://doi.org/10.1007/978-1-59745-471-1
isbn_softcover978-1-62703-834-8
isbn_ebook978-1-59745-471-1Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2009
The information of publication is updating

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发表于 2025-3-21 21:45:29 | 显示全部楼层
Construction of Gene-Targeting Vectors by Recombineeringof knockout vectors has been greatly facilitated by recombineering as it allows one to choose any genomic region to manipulate. We describe here an efficient recombineering-based protocol for making mouse conditional knockout targeting vectors.
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Gene-Trap Vectors and Mutagenesish-throughput use, in an effort to inactivate all genes in the mouse genome. Gene trapping is performed with vectors that simultaneously inactivate and report the expression of the trapped gene and provide a molecular tag for its rapid identification. Gene-trap approaches have been used successfully
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Chromosome Engineering in ES Cellsr phenotypically neutral. To understand the genetic consequences of such genomic changes, these mutations need to be modelled in experimentally tractable systems. The mouse is an excellent organism for this analysis because of its biological and genetic similarity to humans, the ease with which its
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Generation of shRNA Transgenic Miceeasy manner. For the use of RNAi in mice, short hairpin (sh) RNAs expressed stably from the genome are a faster alternative to conventional knockout approaches. Here, we describe an advanced strategy for complete or conditional gene knockdown in mice, where the Cre/loxP system is used to activate RN
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Gene Targeting in Mouse Embryonic Stem Cellsr ability to alter the mouse genome has been limited by both the lack of technologies to conditionally target a locus and by conventional cloning. The “cre/loxP” and “recombineering” technologies have overcome some of these limitations and have greatly enhanced our ability to manipulate the mouse ge
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