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Related Concept Videos

RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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Nucleic Acid Structure01:25

Nucleic Acid Structure

The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA has a double-helix structure. The...

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Related Experiment Video

Updated: Jul 1, 2026

Protocol for the Solid-phase Synthesis of Oligomers of RNA Containing a 2'-O-thiophenylmethyl Modification and Characterization via Circular Dichroism
11:37

Protocol for the Solid-phase Synthesis of Oligomers of RNA Containing a 2'-O-thiophenylmethyl Modification and Characterization via Circular Dichroism

Published on: July 28, 2017

A convenient approach towards 2'-O-modified RNA-oligonucleotides on solid support using universal nucleosides.

Jens Haas1, Joachim W Engels

  • 1Johann Wolfgang Goethe-University Frankfurt, Department of Chemistry, D-60438 Frankfurt am Main, Germany.

Nucleic Acids Symposium Series (2004)
|September 9, 2008
PubMed
Summary

Researchers developed a new method for modifying RNA oligonucleotides on solid supports. This efficient technique utilizes universal nucleosides with a 2'–O-aminopropyl–tether for improved synthesis.

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Nucleoside Triphosphates - From Synthesis to Biochemical Characterization

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Last Updated: Jul 1, 2026

Protocol for the Solid-phase Synthesis of Oligomers of RNA Containing a 2'-O-thiophenylmethyl Modification and Characterization via Circular Dichroism
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Nucleoside Triphosphates - From Synthesis to Biochemical Characterization
15:22

Nucleoside Triphosphates - From Synthesis to Biochemical Characterization

Published on: April 3, 2014

Area of Science:

  • Chemical Synthesis
  • Oligonucleotide Chemistry
  • Biotechnology

Background:

  • Solid-phase synthesis is crucial for producing RNA oligonucleotides.
  • Modifications enhance RNA functionality but can be challenging to implement.
  • A need exists for efficient and versatile modification strategies.

Purpose of the Study:

  • To introduce a novel synthetic pathway for RNA oligonucleotide modification.
  • To demonstrate the utility of universal nucleosides with a specific tether for solid-phase synthesis.
  • To enable efficient and versatile modifications of RNA.

Main Methods:

  • Development of a novel synthetic route for RNA modification.
  • Utilizing universal nucleosides functionalized with a 2 -O-aminopropyl-tether.
  • Performing modifications on solid-support.

Main Results:

  • An efficient synthetic pathway for RNA oligonucleotide modification was established.
  • The 2 -O-aminopropyl-tether proved effective for solid-phase synthesis.
  • The method allows for versatile and efficient modification of RNA.

Conclusions:

  • The reported method offers an efficient approach for RNA oligonucleotide modification.
  • This strategy facilitates the synthesis of modified RNA with potential applications in therapeutics and diagnostics.
  • The use of universal nucleosides with the 2 -O-aminopropyl-tether represents a significant advancement in oligonucleotide chemistry.