Literature DB >> 12757390

New reagents for the introduction of reactive functional groups into chemically synthesized DNA probes.

Zbigniew Skrzypczynski1, Sarah Wayland.   

Abstract

An efficient and versatile preparative approach is described, allowing for the preparation of DNA probes modified with an aldehyde group at the 3'- or 5'-end. The developed synthetic strategy allows for the preparation of a new family of phosphoramidites and solid supports compatible with the automated synthesis of modified oligonucleotide probes. These new reagents were prepared from intermediates 3 and 3a, obtained from the commercially available aleuritic acid 1. It was demonstrated that the new phosphoramidite reagents also could be used as new types of cleavable linkers. A new and efficient method for the production of 5' aldehyde-labeled DNA probes was developed.

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Year:  2003        PMID: 12757390     DOI: 10.1021/bc025657j

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  2 in total

1.  Linker phosphoramidite reagents for the attachment of the first nucleoside to underivatized solid-phase supports.

Authors:  Richard T Pon; Shuyuan Yu
Journal:  Nucleic Acids Res       Date:  2004-01-29       Impact factor: 16.971

2.  Fluorocarbons Enhance Intracellular Delivery of Short STAT3-sensors and Enable Specific Imaging.

Authors:  Valeriy Metelev; Surong Zhang; Shaokuan Zheng; Anand T N Kumar; Alexei Bogdanov
Journal:  Theranostics       Date:  2017-08-03       Impact factor: 11.556

  2 in total

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