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Titlebook: RNA; Methods and Protocol Henrik Nielsen Book 2011 Springer Science+Business Media, LLC 2011 Bioinformatics.Mammalian genome.Messenger RNAs

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書目名稱RNA
副標題Methods and Protocol
編輯Henrik Nielsen
視頻videohttp://file.papertrans.cn/821/820144/820144.mp4
概述Features samples for subsequent analysis by high-throughput technologies, such as deep sequencing or microarray analysis -Contains thorough, detailed methods and protocols easily implemented by novice
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: RNA; Methods and Protocol Henrik Nielsen Book 2011 Springer Science+Business Media, LLC 2011 Bioinformatics.Mammalian genome.Messenger RNAs
描述Recent insight into the transcripts generated from the mammalian genome (i.e. the transcriptome) has revealed that transcription is a far more complex phenomenon than previously thought.In RNA: Methods and Protocols, expert researchers provide the procedures and methods used to describe the structure of messenger RNAs and non-coding RNAs that are transcribed by RNA polymerase II as the immediate gene products in mammalian cells.Focused on the structure of the RNA products of “gene X” and the mapping of proteins associated with these RNAs, the volume presents appropriate information for non-specialists in RNA biology. Written in the highly successful Methods in Molecular Biology? series format, many chapters contain introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and key tips on troubleshooting and avoiding known pitfalls.Comprehensive and practical, RNA: Methods and Protocols views the transcriptional landscape with an appreciation for the role that proteins play in the processing and interpretation of genetic information in an attempt to further our crucial knowledge of the many produ
出版日期Book 2011
關(guān)鍵詞Bioinformatics; Mammalian genome; Messenger RNAs; Microarray analysis; Non-coding RNAs; Protein mapping; R
版次1
doihttps://doi.org/10.1007/978-1-59745-248-9
isbn_softcover978-1-4939-5643-2
isbn_ebook978-1-59745-248-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC 2011
The information of publication is updating

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Working with RNAk rules have to be implemented to maintain the integrity of the RNA. Alkaline pH, high temperatures, and heavy metal ions should be avoided when possible and ribonucleases kept in check. The chapter outlines the specific precautions recommended for work with RNA and describes some of the modificatio
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Synthesis of RNA by In Vitro Transcriptionto those of several kilobases in μg to mg quantities. It is based on the engineering of a template that includes a bacteriophage promoter sequence (e.g. from the T7 coliphage) upstream of the sequence of interest followed by transcription using the corresponding RNA polymerase. In vitro transcripts
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Efficient Poly(A)+ RNA Selection Using LNA Oligo(T) Capturepoly(A). RNA directly from guanidinium thiocyanate (GuSCN)-containing cell or tissue extract by combining the design of biotinylated LNA oligo(T) capture probes with subsequent immobilization of the captured poly(A). RNA onto streptavidin-coated magnetic particles. In contrast to DNA oligo-dT and po
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Rapid Amplification of cDNA Ends (RACE)ly known. Starting with an mRNA mixture, gene-specific primers generated from the known regions of the gene and non-specific anchors, full-length sequences can be identified in as little as 3 days. RACE can also be used to identify alternative transcripts of a gene when the partial or complete seque
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Fractionation of mRNA Based on the Length of the Poly(A) Taile mRNAs according to the length of the poly(A) tail. Poly(A) fractionation can be used to detect small changes in poly(A) tail length or to prepare samples for microarray analysis. RNA or crude lysate is mixed with biotinylated oligo(dT), which is then bound to paramagnetic streptavidin beads. Oligo
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