Phosphoramidite for the installation of 7-Deaza-G residues in G-rich regions of oligos to disrupt unwanted hydrogen bonding.
This convertible phosphoramidite allows the formation of N4-alkyl-dC residues.
Isosteric with adenine but offers a different pi-electron distribution and thus an altered dipole moment.
Phosphoramidite for the incorporation of 5-methoxy-uridine into an oligonucleotide.
Small, fluorescent natural base mimic that can signal the presence of abasic sites in hybridized DNA oligonucleotides.
A phosphoramidite that is an isosteric analogue of dG.
Useful mixed-modified phosphoramidite.
An adenosine analogue with the hydrogen bond donor deleted.
Enables incorporation of pseudouridine into RNA.
Universal base phosphoramidite.
Useful degenerate base phosphoramidite that pairs with C or T.
An adenosine analogue with the hydrogen bond donor deleted.
Useful degenerate base phosphoramidite that pairs with A or G.
Smallest member of the "steric phosphoramidite tool box" for probing the steric requirements at N2 of dG in various applications.
Phosphoramidite for internal or 5'-incorporation of a deaza-modified dG nucleobase into an oligonucleotide.
Phosphoramidite replacement for dC that enhances base-pairing.
Convertible phosphoramidite that allows the formation of N6-alkyl-dA residues through reaction with alkyl amines.
Useful phosphoramidite for modification of base pairing and metal chelating characterisitcs of purine nucleosides through elimination of the N7 nitrogen.
Useful mixed-modified phosphoramidite.
Useful addtion to the nebularine family for hydrogen bonding studies.
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