Useful disulfide synthon.
Monofluoro-substituted cyclooctyne (MFCO) suitable for copper-free Click reactions.
CPG column used to incorporate a thiol functionality, with ether spacer, at the 3' end of an oligonucleotide.
Linker useful in Click Chemistry reactions.
Useful azide synthon for downstream Click Chemistry applications.
Used to incorporate a folate functionality into biomolecules by Click Chemistry, for recognition by overexpressed folate receptors in cancer cells.
Allows the introduction of a 5-aminoallyl-deoxyuridine residue into oligonucleotides for the purpose of post-synthetic labeling by acylation.
Phosphoramidite used to incorporate an amino-modified dT into an oligonucleotide, with a 15-atom spacer.
Amino-functionalised linker synthon.
Phosphoramidite for the incorporation of a 2-thiodeoxythymidine modification into oligonucleotides.
A bi-functional linker with potential applications in oligonucleotide Click ligations.
Useful amine-modified deoxyguanosine phosphoramidite, with a C6 spacer.
Used to incorporate a desthiobiotin functionality into biomolecules, for ligation via Saudinger ligation or Click Chemistry.
Phosphoramidite for the incorporation of a carboxylate function either internally or at the 5' end of an oligonucloetide, with a dT nucleobase.
CPG column for the incorporation of an amino function at the 3' end of an oligonucleotide.
An amino-modifier phosphoramidite with an acid-labile DMT protecting group.
Used to incorporate cholesterol functionality into biomolecules via Click Chemistry.
Phosphoramidite for the efficient incorporation of a 2-thiouridine modification into oligonucleotides.
Allows incorporation of a useful hydrazine moiety for post-synthetic modification of oligonucleotides, with spacer.
Phosphoramidite used to incorporate a 8-amino-modified deoxyguanosine into an oligonucleotide.
Reactive functional groups, such as primary amine, thiol, and carboxylate, are incorporated into oligos to enable post-synthesis conjugation with various affinity, reporter, and protein labels, as well as solid surfaces such as glass slides and gold microspheres.
Using reactive functional groups is useful for incorporating modifications that are unavailable as phosphoramidites or unstable during oligonucleotide synthesis and deprotection.
For most of the modifications, we offer phosphoramidites and reagents for incorporation to your oligo at the 3’-end, 5’-end, and internally. The reagents are available with various linker types (TEG, carbon) and protective agents (e.g., Fmoc, MMT).
Acrydite-modified oligos covalently react with thiol-modified surfaces or can be used in polyacrylamide gels during polymerization.
The aldehyde function is often used to conjugate biopolymers to other molecules via reductive amination or adduct formation with hydroxylamines, hydrazines, and semicarbazides. You can also use aldehydes to immobilize oligos onto solid surfaces.
We offer a wide range of phosphoramidites, CPG, and other reagents for incorporating amino functionalities at the 5’- and 3’-ends of an oligo or internally. You can choose the type of linker (e.g., carbon, TEG), linker length (C3 to C12), and protection group (e.g., TFA, MMT, Fmoc) that best suit your applications.
Carboxylate modifiers can be used to introduce a carboxylic acid function at the 5’-end of an oligonucleotide that is available for conjugation to amines whilst still on the solid support. This strategy avoids the problems of low yields, long reaction times and the need for excess reactants often encountered by other post-cleavage solution methods. Internal carboxylate function can also be achieved.
We offer a wide range of Click Chemistry reagents which can be used as reliable labelling methods. Our Click-mates™ collection includes alkynes for the classic Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click reaction”, as well as the streamlined copper-free click modifications. The Click-easy™ alkynes can help you to simplify bioconjugation work by employing cyclo-alkynes for efficient uncatalyzed click ligation.
We offer glyceryl CPG to incorporate a glyceryl functionality at the 3' end of an oligo which is readily oxidized to an aldehyde or further oxidized to the corresponding carboxylic acid. Either the aldehyde or the carboxylate may be used for conjugation to amino-functionalised biomolecules. This is an effective strategy for 3' post-synthetic modification with amines, as 3'-functionalised carboxylate and aldehyde solid supports are not commonly available.
We offer hydrazide phosphoramidites to incorporate a useful hydrazine moiety at the 5’-end of an oligo for use with post-synthesis covalent attachment chemistry.
Thiol groups are often used to attach labels, such as fluorescent tags and biotin. Conjugation to a thiol is orthogonal to that of an amino functionality; it is not uncommon to have both groups in the same oligo (e.g., 3’-amino and 5’-thiol).
Thioctic acid is particularly useful for conjugating an oligo to gold and silver nanoparticles, making it important for biosensing technologies and self-assembling DNA applications.