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Titlebook: cDNA Library Protocols; Ian G. Cowell,Caroline A. Austin Book 1997 Springer Science+Business Media New York 1997

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发表于 2025-3-21 19:00:08 | 显示全部楼层 |阅读模式
书目名称cDNA Library Protocols
编辑Ian G. Cowell,Caroline A. Austin
视频video
丛书名称Methods in Molecular Biology
图书封面Titlebook: cDNA Library Protocols;  Ian G. Cowell,Caroline A. Austin Book 1997 Springer Science+Business Media New York 1997
描述The first libraries of complementary DNA (cDNA) clones were con­ structed in the mid-to-late 1970s using RNA-dependent DNA polymerase (reverse transcriptase) to convert poly A* mRNA into double-stranded cDNA suitable for insertion into prokaryotic vectors. Since then cDNA technology has become a fundamental tool for the molecular biologist and at the same time some very significant advances have occurred in the methods for con­ structing and screening cDNA libraries. It is not the aim of cDNA Library Protocols to give a comprehensive review of all cDNA library-based methodologies; instead we present a series of up-to-date protocols that together should give a good grounding of proce­ dures associated with the construction and use of cDNA libraries. In deciding what to include, we endeavored to combine up-to-date versions of some of the most widely used protocols with some very usefiil newer techniques. cDNA Library Protocols should therefore be especially useful to the investigator who is new to the use of cDNA libraries, but should also be of value to the more experienced worker. Chapters 1—5 concentrate on cDNA library construction and manipula­ tion, Chapters 6 and 7 describe me
出版日期Book 1997
版次1
doihttps://doi.org/10.1385/089603383X
isbn_softcover978-1-4899-4050-6
isbn_ebook978-1-59259-555-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 1997
The information of publication is updating

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Applications in Statistical Computingn the λ vector (.). Once a Lambda ZAP library is constructed and amplified, putative clones or the λ library itself may be excised into the phagemid form. Two versions of the excision protocol for Lambda ZAP-based vectors are included here.
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,Clone Excision Methods for the Lambda ZAP®-Based Vectors,n the λ vector (.). Once a Lambda ZAP library is constructed and amplified, putative clones or the λ library itself may be excised into the phagemid form. Two versions of the excision protocol for Lambda ZAP-based vectors are included here.
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Review of the Development of Energy Finance cells in a tissue are expressing genes of interest or the tissue is in limited supply. A cDNA library from the targeted cells is preferable to a library constructed from the entire tissue containing these cells, because in the latter case, genes expressed in the targeted cells may be too rare to be
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Sibel Soylu,İlkay Şendeniz-Yüncü,Uğur Soytaşr regionally, temporally, or environmentally specific), a large proportion of all transcripts (approx 40–45%) represent low-abundance mRNAs, present at 1–20 molecules/cell (.). In a given cell type, “low-abundance” mRNAs are likely to represent >95% of the different mRNAs expressed. The lower the ab
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Review of the Development of Energy Financeof RNA can be made from several grams of tissue or as little as 50 mg. However, large samples are generally more representative of the genes expressed in a population of plants in response to environmental cues or at a defined stage of development. Therefore, large-scale extraction of RNA is the met
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Wolfgang Gaul,Christoph Winkler The approach described here to clone the missing sequence (cDNA ends) employs polymerase chain reaction (PCR). Since the initial reports of rapid amplification of cDNA ends (RACE) (.) or related techniques (.,.), many labs have developed significant improvements on the basic approach (.–.). The mos
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