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Titlebook: Agrobacterium Protocols; Volume I Kan Wang Book 2006Latest edition Humana Press 2006 Agrobacterium tumefaciens.Arabidopsis thaliana.DNA.Flo

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發(fā)表于 2025-3-21 18:43:39 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Agrobacterium Protocols
期刊簡稱Volume I
影響因子2023Kan Wang
視頻videohttp://file.papertrans.cn/152/151687/151687.mp4
發(fā)行地址Includes supplementary material:
學(xué)科分類Methods in Molecular Biology
圖書封面Titlebook: Agrobacterium Protocols; Volume I Kan Wang Book 2006Latest edition Humana Press 2006 Agrobacterium tumefaciens.Arabidopsis thaliana.DNA.Flo
影響因子Agrobacterium tumefaciens is a soil bacterium that for more than a century has been known as a pathogen causing the plant crown gall disease. Unlike many other pathogens, Agrobacterium has the ability to deliver DNA to plant cells and permanently alter the plant genome. The discovery of this unique feature 30 years ago has provided plant scientists with a powerful tool to genetically transform plants for both basic research purposes and for agricultural development. Compared to physical transformation methods such as particle bomba- ment or electroporation, Agrobacterium-mediated DNA delivery has a number of advantages. One of the features is its propensity to generate a single or a low copy number of integrated transgenes with defined ends. Integration of a single transgene copy into the plant genome is less likely to trigger “gene silencing” often associated with multiple gene insertions. When the first edition of Agrobacterium Protocols was published in 1995, only a handful of plants could be routinely transformed using Agrobacterium. Agrobacterium-mediated transformation is now commonly used to introduce DNA into many plant species, including monocotyledon crop species that wer
Pindex Book 2006Latest edition
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Three Methods for the Introduction of Foreign DNA into ,ormable plant cells through the use of T-DNA binary vectors. Three methods are commonly used. Transformation with purified plasmid can be done with either electroporation or a simple freeze/thaw transformation method. Alternatively, a mobilizable plasmid can be placed into . using the triparental ma
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Nucleic Acid Extraction from , Strainsells often requires the manipulation and analysis of nucleic acids present in recombinant . strains. Here we present dependable methods for the isolation of genomic (total) DNA, mega-plasmid DNA, shuttle or binary plasmid DNA, and RNA. In addition, we provide a simple method for the electronic trans
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Virulence Gene Inductionion as a two-component regulatory system to sense particular phenolic compounds synthesized by wounded plant tissues. Induction by these phenolic compounds, in the presence of certain neutral or acid sugars, results in activation of other . genes, leading to the processing of T-DNA from the Ti-plasm
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Floral Dip Transformation Methodsequently set seed, and transgenic plants are then selected among the progeny seedlings. Because no plant tissue culture is required, somaclonal variation is avoided, and the procedure can be performed easily by nonspecialists. Success rates are high: it is common that 1% of the progeny seedlings ar
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Transformation Using Cotyledon Explantse genotype Jemalong A17 is in progress. By using cotyledons as explants for . infection and direct shoot formation, this protocol allows for rapid production of transgenic plants from A17 and other genotypes. Transgenic plants can be regenerated and established in the greenhouse in only 3-4 mo after
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Transformation Using Root Explantstions, including nodulation and mycorrhizal colonization. The development of different transformation methods is an important aspect for functional genomic studies in the species. This protocol describes an efficient system for generating transgenic plants from . roots based on .-mediated transforma
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