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Titlebook: DNA Sequencing Protocols; Hugh G. Griffin,Annette M. Griffin Book 19931st edition Springer Science+Business Media New York 1993

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书目名称DNA Sequencing Protocols
编辑Hugh G. Griffin,Annette M. Griffin
视频videohttp://file.papertrans.cn/261/260196/260196.mp4
丛书名称Methods in Molecular Biology
图书封面Titlebook: DNA Sequencing Protocols;  Hugh G. Griffin,Annette M. Griffin Book 19931st edition Springer Science+Business Media New York 1993
描述The purpose of DNA Sequencing Protocols is to provide detailed practical procedures for the widest range of DNA sequencing meth­ ods, and we believe that all the vanguard techniques now being applied in this fast-evolving field are comprehensively covered. Sequencing technology has advanced at a phenomenal rate since the original methods were first described in the late 1970s and there is now a huge variety of strategies and methods that can be employed to determine the sequence of any DNA of interest. More recently, a large number of new and innovative sequencing techniques have been developed, including the use of such novel polymerases as Tag poly­ merase and Sequenase, the harnessing of PCR technology for linear amplification (cycle) sequencing, and the advent of automated DNA sequencers. DNA sequencing is surely one of the most important techniques in the molecular biology laboratory. Sequence analysis is providing an increasingly useful approach to the characterization of biological systems, and major multinational projects are already underway to map and sequence the entire genome of organisms, such as Escherichia coli, Saccharomyces cerevisiae, Caenorhabditis elegans, and H
出版日期Book 19931st edition
版次1
doihttps://doi.org/10.1385/0896032485
isbn_ebook978-1-59259-510-5Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 1993
The information of publication is updating

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K. Bennaceur,Z. Sahraoui,M. A. Nacersis of the labeled strands can easily be synthesized in automatic synthesizers or by hand, the latter of which is more laborious. Various so-called "universal sequencing" and "reverse sequencing" primers, complementary to the beginning of the polylinker region in M13 . cloning phages and plasmids, a
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Transfection of E. coli with M13 DNA,ficiency in some or all strains of . that have been tested. The mechanisms involved in DNA transformation of cells are not fully understood and even with the most efficient methods that are available the proportion of cells that become “competent” for transformation is limited to around 10% of the t
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