X,5'-Cyanine 5 CE-Phosphoramidite
Phosphoramidite used to incorporate the cyanine 5 fluorophore internally or at the 5’ end of an oligonucleotide.
Phosphoramidite used to incorporate the cyanine 5 fluorophore internally or at the 5’ end of an oligonucleotide.
Convertible nucleoside phosphoramidite that allows the formation of N4-alkyl-C residues in RNA for structural studies.
Used as a labeling probe for intracellular proteins.
A convertible nucleoside phosphoramidite that allows the formation of N2-alkyl-G residues in RNA for structural studies.
Useful linker synthon.
A fluorescent nucleoside phosphoramidite useful for probing the characterisitcs of DNA repair complexes.
Phosphoramidite used to incorporate a 5-hydroxy-modified deoxycytidine into an oligonucleotide for epigenetic studies.
Phosphoramidite used to incorporate a 2’-O-methoxyethyl-modified methyl-U into an oligonucleotide, useful for antisense RNA.
Des-methyl analog of cytidine useful for probing the hydrogen-bonding characterisitcs in oligonucleotides.
Phosphoramidite used to incorporate a BlackBerry-650™ moiety either internally or at the 5' end of an oligonucleotide.
Phosphoramidite for the synthesis of oligonucleotides bearing a 5'-aminooxy group.
Useful building block for incorporation of the psoralen ring system.
Acrylic phosphoramidite that can be added to oligonucleotides as a 5’-modification for thiol conjugation.
Useful amino-modified deoxyadenosine phosphoramidite.
Phosphoramidite for incorporation of a 6-thio-modified guanosine in a synthetic oligonucleotide.
Phosphoramidite useful for synthesising 2'-5' linked oligonucleotides.
Phenoxyacetyl (Pac) protected 2'-OTBDMS phosphoramidite for the incorporation of ribo-A into a synthetic oligonucleotide using UltraMILD conditions.
Phosphoramidite for the incorporation of an amino function at the 5' end of an oligonucleotide.
Phosphoramidite for incorporation of cholesterol internally or at 5' end of an oligonucleotide, with a triethylene glycol spacer.
Half of a novel base pair (with d5SICS) that achieves pair recognition through hydrophobic interactions.
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