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Titlebook: Agrobacterium Protocols; Volume II Kan Wang Book 2007Latest edition Humana Press 2007 DNA.Flora.algae.arabidopsis thaliana.fungi.genetic en

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發(fā)表于 2025-3-21 17:04:52 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Agrobacterium Protocols
期刊簡(jiǎn)稱Volume II
影響因子2023Kan Wang
視頻videohttp://file.papertrans.cn/152/151690/151690.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 II Kan Wang Book 2007Latest edition Humana Press 2007 DNA.Flora.algae.arabidopsis thaliana.fungi.genetic en
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 agric- tural 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 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. Ag- bacterium-mediated transformation is now commonly used to introduce DNA into many plant species, including monocotyledon crop species that were
Pindex Book 2007Latest edition
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Cassava (, Crantz)ted transformation systems are routinely used to engineer cassava. These systems use either somatic embryos or friable embryogenic calli. This paper presents detailed protocols for the transformation of cassava using primary somatic embryos. The effects of explant types, tissue culture conditions, a
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Bermudagrass (, spp.)ent protocol that allows for the generation of a large number of transgenic bermudagrass plants, bypassing the callus formation phase. Stolon nodes are infected and co-cultivated with . harboring pCAMBIA binary vectors. Hygromycin phosphotransferase gene (.) is used as the selectable marker and hygr
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Perennial Ryegrass (, L.)ein (sgfpS65T) reporter gene is introduced in combination with the .II selectable marker gene into axillary bud derived embryogenic calli of perennial ryegrass (. L.) by co-cultivation with . strain AGL0 harboring binary vector pYF132. Following the co-cultivation calli are cultured for 48 h in liqu
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Switchgrass (, L.)So far, switchgrass is the only warm season grass that has been transformed with .. We have developed a highly efficient system for transformation of different switchgrass explants utilizing the . strain AGL1 carrying the binary vector pDM805, containing the phosphinotricin acetyltransferase (.) and
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Tall Fescue (, Schreb.) chapter describes a protocol that allows for the generation of large number of transgenic tall fescue plants by .-mediated transformation. Embryogenic calli induced from caryopsis are used as explants for inoculation with .. The . strain used is EHA105. Hygromycin phosphotransferase gene (.) is use
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