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Working together to meet the demand for SARS-CoV-2 probes and primers

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Universal base phosphoramidite.

A fluorescent analogue of cytidine.

Convertible nucleoside phosphoramidite that allows the formation of N4-alkyl-C residues in RNA for structural studies.

Des-methyl analog of cytidine useful for probing the hydrogen-bonding characterisitcs in oligonucleotides.

Useful amino-modified deoxyadenosine phosphoramidite.

Useful amino-modified deoxyadenosine phosphoramidite.

A stable phosphoramidite analogue of N3-methyladenine (3-Me-A).

Photochromic nucleoside (PCN) phosphoramidite that provides reversible duplex regulation via a light induced trans-cis isomerization.

Useful for incorporating 7-Deaza-modified guanosine into oligonucleotides to disrupt unwanted hydrogen bonding.

A convertible nucleoside phosphoramidite that allows the formation of N2-alkyl-G residues in RNA for structural studies.

A fluorescent nucleoside phosphoramidite useful for probing the characterisitcs of DNA repair complexes.

Features a nucleobase that is isosteric with adenine but offers a different pi-electron distribution.

Useful modified deoxyctidine phosphoramidite.

Useful addtion to the nebularine family for hydrogen bonding studies.

Useful phosphoramidite for oxidative studies of thymidine.

The C-nucleoside 2'-deoxypseudouridine, in contrast to dU, forms stable C:pseudoU-A triplets.

Phosphoramidite enables incorporation of a nitrogen atom in place of the methine group at position 6 of the thymine ring in oligonucleotides.

Phosphoramidite enables incorporation of an N3-o-anisoyl protected 6-aza-dU residue into oligonucleotides.

Phosphoramidite used to incorporate N1-Methylpseudouridine into oligonucleotides for the investigation of RNA methylation .

A C-nucleoside phosphoramidite that is isosteric with deoxycytidine and has additional hydrogen-bonding ability.

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