5'-DMT-dU-Suc-CPG (5'-DMT-deoxyUridine CPG) Column
CPG used to incorporate a deoxyuridine base into the 3' end of an oligonucleotide.
CPG used to incorporate a deoxyuridine base into the 3' end of an oligonucleotide.
CPG used to incorporate a deoxyinosine base into the 3' end of an oligonucleotide.
Phosphoramidite used to incorporate a 5-methyl-modified deoxycytidine into an oligonucleotide.
Phosphoramidite used to incorporate a 5-nitro-modified indole "universal" base into an oligonucleotide.
CPG column used to incorporate a deoxyuridine base into the 3' end of an oligonucleotide.
CPG column used to incorporate a 5-methyl-modified deoxycytidine into the 3' end of an oligonucleotide.
CPG column used to incorporate a deoxyinosine base into the 3' end of an oligonucleotide.
Phosphoramidite used to replace thymidine residues in oligonucleotides, for duplex stabilization.
Half of a novel base pair (with dNaM) that achieves pair recognition through hydrophobic interactions.
Phosphoramidite used to incorporate a furanocoumarin into an oligonucleotide, with a C6 spacer.
Guanosine analogue phosphoramidite which lacks the O6 carbonyl_x000D_ resulting in a_x000D_ hydrogen bonding pattern isomeric_x000D_ with that of adenosine.
Phosphoramidite used to incorporate alkyne-U functionality into an oligonucleotide for coupling reactions.
Tricyclic fluorescent dC nucleoside analogue.
Half of a novel base pair (with d5SICS) that achieves pair recognition through hydrophobic interactions.
Phosphoramidite used to incorporate an anthraquinone group into an oligonucleotide, either internally or at 5' end.
Useful phosphoramidite for the incorporation of 2'-deoxyxanthosine (dX) nucleotides into oligonucleotides.
Tricyclic fluorescent dC nucleoside analogue.
Phosphoramidite used to incorporate a 2-amino-modified deoxyadenosine into an oligonucleotide.
Nucleoside phosphoramidite useful in Click Chemistry reactions.
FRET acceptor for tricyclic fluorescent dC nucleoside analogues.
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