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Titlebook: Differential-Display Reverse Transcription-PCR (DDRT-PCR); Sergio Colonna-Romano,Antonella Leone,Bruno Maresc Book 1998 Springer-Verlag Be

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書(shū)目名稱Differential-Display Reverse Transcription-PCR (DDRT-PCR)
編輯Sergio Colonna-Romano,Antonella Leone,Bruno Maresc
視頻videohttp://file.papertrans.cn/279/278844/278844.mp4
概述First manual describing this new technique.Easy to follow step-by-step instructions.Practical hints and experimental strategies are given for every protocol
叢書(shū)名稱Springer Lab Manuals
圖書(shū)封面Titlebook: Differential-Display Reverse Transcription-PCR (DDRT-PCR);  Sergio Colonna-Romano,Antonella Leone,Bruno Maresc Book 1998 Springer-Verlag Be
描述Identification of differentially expressed genes is one of the major challenges in molecular biology. Several techniques allow the cloning of such sequences. However, methods such as RNA subtraction or differential hybridization are time-consuming and require large amounts of mRNA..Recently, a new approach has successfully been developed: Differential-Display Reverse Transcription-PCR (DDRT-PCR). This technique has been proven to be highly effective in identifying sequences that are differentially expressed in various cell types. The most striking advantage is, however, that only nanograms of total RNA are sufficient. Thus every mRNA species expressed in the cell system can be investigated, even those present at very low levels.
出版日期Book 1998
關(guān)鍵詞DNA; Gene; Molekulargenetik; PCR; RNA; Zelldifferenzierung; differentiation; genes; mRNA; molecular genetics;
版次1
doihttps://doi.org/10.1007/978-3-642-80454-0
isbn_softcover978-3-540-63297-9
isbn_ebook978-3-642-80454-0
copyrightSpringer-Verlag Berlin Heidelberg 1998
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Preference from Priorities: Static Logicmplified cDNAs (Fig. 1). Nondenaturing gels can also be used to display differentially expressed bands. However, nondenaturing gels have not replaced denaturing ones, since both incompletely annealed single-stranded cDNAs and heteroduplexes (produced by errors of Taq polymerase) from the same gene m
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Preference over Worlds: Static Logicluted from the dried gel for further analysis. The accuracy of the cut-out depends on proper alignment of the gel and autoradiograph. Several tricks, such as marking the profile of the gel onto the film, making pinholes through the gel and film, or dotting the gel with fluorescent or radioactive dye
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Common Reasoning in a Computational Contextwever, if smearing or multiple bands appear in PCR products, it is necessary to purify the reamplified cDNA prior to subcloning. Many commercial kits (l.e., QIAquick Gel extraction Kit, Qiagen) allow rapid purification in only a few steps and are relatively inexpensive.
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Quantities, laws and sign conventionss. The sequence of a deoxyribonucleic acid molecule can be determined by chemical (Maxam and Gilbert 1977, 1980) or enzymatic (Sanger et al. 1977) methods. The enzymatic sequencing method is based on the ability of DNA polymerase to extend a primer hybridized to the template to be sequenced until a
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A Two-Level Perspective on PreferenceThe purity and integrity of isolated RNA are essential prerequisites for a successful analysis of differential gene expression by DDRT-PCR. Thus extreme care should be taken during all the steps of RNA preparation.
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