- Life Science
- In vitro diagnostics
- Synthesis of oligonucleotides
- Primers
- Fluorescently labeled probes and samples
- Oligonucleotides GentaOligoPure
- Modifications
- ‘Click’ chemistry modifications
- 2'-F (2'-Fluoro) RNA modification
- Phosphorothioate bonds
- 2'-MOE (2'-O-Methoxyethyl) RNA modification
- 2'-OMe (2'-O-Methyl) RNA modification
- LNA (Locked Nucleic Acid) RNA modification
- Other modifications
- Phosphorylation
- Thiophosphate bonds
- Fluorophores and quenchers
- Linkers and functionalization
- Reagents for molecular biology
- Services
2'-F (2'-Fluoro) RNA modification
2’-Fluoro RNA oligonucleotides contain fluorine atom at 2'-position of sugar moiety instead of native 2'-hydroxy group that slightly increases binding affinity (melting temperature, Tm) to RNA and nuclease resistance. Unique features of 2’-fluoro nucleotides – preferred 2’-exo-3’-endo conformation of the sugar ring and the size of fluorine atom being close to hydroxy group, makes this modification the closest mimic of natural ribonucleotides. 2’-Fluoro oligonucleotides are beneficial for many applications including Antisense oligonucleotides, ribozymes, aptamers and siRNA.
Available sites for modifications are 5’, internal, and 3’.
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