Titlebook: RNA-Protein Complexes and Interactions; Methods and Protocol Ren-Jang Lin Book 2016 Springer Science+Business Media New York 2016 RNA-bindi

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書目名稱RNA-Protein Complexes and Interactions影響因子(影響力)




書目名稱RNA-Protein Complexes and Interactions影響因子(影響力)學(xué)科排名




書目名稱RNA-Protein Complexes and Interactions網(wǎng)絡(luò)公開度




書目名稱RNA-Protein Complexes and Interactions網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱RNA-Protein Complexes and Interactions被引頻次




書目名稱RNA-Protein Complexes and Interactions被引頻次學(xué)科排名




書目名稱RNA-Protein Complexes and Interactions年度引用




書目名稱RNA-Protein Complexes and Interactions年度引用學(xué)科排名




書目名稱RNA-Protein Complexes and Interactions讀者反饋




書目名稱RNA-Protein Complexes and Interactions讀者反饋學(xué)科排名

ARBOR

膠狀

Ren-Jang LinIncludes cutting-edge methods and protocols for studying RNA-protein interactions.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the

aneurysm

labyrinth

Polydipsia

Single-Turnover Kinetics of Methyl Transfer to tRNA by Methyltransferases,s can be directly assigned to the steps associated with the chemistry of methyl transfer, including the substrate binding affinity to the methyltransferase, the pre-chemistry re-arrangement of the active site, and the chemical step of methyl transfer. An additional advantage is that kinetic constant

FIS

,Genome-Wide Profiling of RNA–Protein Interactions Using CLIP-Seq,ence genome and the identification of the crosslinking sites. Meanwhile, one or more amino acids of a crosslinked RBP can remain attached to its bound RNA due to incomplete digestion of the protein. As a result, reverse transcriptase may not read through the crosslink sites, and produce cDNA ending

流浪者

Informational Suppression to Probe RNA:RNA Interactions in the Context of Ribonucleoproteins: U1 anr U1” snRNAs with restored base-pairing to mutant 5′ss in different registers. Cells are transfected with combinations of minigenes and suppressor U1s, and the splicing patterns are analyzed by reverse transcription and semiquantitative PCR, followed by gel electrophoresis. The identity of suppresso

GNAT

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