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Titlebook: E. coli Plasmid Vectors; Methods and Applicat Nicola Casali,Andrew Preston Book 20031st edition Springer Science+Business Media New York 20

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書(shū)目名稱(chēng)E. coli Plasmid Vectors
副標(biāo)題Methods and Applicat
編輯Nicola Casali,Andrew Preston
視頻videohttp://file.papertrans.cn/301/300217/300217.mp4
概述Includes supplementary material:
叢書(shū)名稱(chēng)Methods in Molecular Biology
圖書(shū)封面Titlebook: E. coli Plasmid Vectors; Methods and Applicat Nicola Casali,Andrew Preston Book 20031st edition Springer Science+Business Media New York 20
描述A comprehensive collection of readily reproducible techniques for the manipulation of recombinant plasmids using the bacterial host E. coli. The authors describe proven methods for cloning DNA into plasmid vectors, transforming plasmids into E. coli, and analyzing recombinant clones. They also include protocols for the construction and screening of libraries, as well as specific techniques for specialized cloning vehicles, such as cosmids, bacterial artificial chromosomes, l vectors, and phagemids. Common downstream applications such as mutagenesis of plasmids, recombinant protein expression, and the use of reporter genes, are also described.
出版日期Book 20031st edition
關(guān)鍵詞BAC; DNA; Escherichia coli; PCR; Promoter; Translation; chromosome; genes; reproducible techniques; transcrip
版次1
doihttps://doi.org/10.1385/1592594093
isbn_softcover978-1-61737-391-6
isbn_ebook978-1-59259-409-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2003
The information of publication is updating

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Extraction of DNA from Agarose Gels, elution of the DNA from the substrate. Other methods include hot phenol extraction of the DNA from the gel. The use of phenol is best avoided if possible because of safety and waste disposal concerns. Presented here are two alternative techniques that avoid these concerns, do not require the purcha
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,Construction of Genomic Libraries in λ-Vectors,cloning sites facilitating the cloning of foreign DNA. In addition, λ-phage vectors have the following advantageous features: high cloning efficiency, a relatively large insert-size capacity, and suitability for screening using nucleic acid probes. In terms of gene screening, genomic DNA libraries a
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Isolation of Plasmids from , by Boiling Lysis,described with different adaptations in a variety of protocol books (.,.). The quality of the isolated plasmid DNA is lower than that from an alkaline lysis miniprep, but it is sufficient for restriction analysis.
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Cloning in Plasmid Vectors,d upon transformation of the recombinant molecule into a bacterial cell (.. and .) so that the DNA of interest can be investigated further. Cloning is an essential part of many experiments, including library generation (..) and expression studies (..).
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E. coli Plasmid Vectors978-1-59259-409-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
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