US2008090959A1PendingUtilityA1
Epoxide polymer surfaces
Est. expirySep 30, 2017(expired)· nominal 20-yr term from priority
C08L 63/00C40B 80/00C40B 40/06B82Y 30/00B01J 2219/00677B01J 2219/00605B01J 2219/00626B01J 2219/00659B01J 2219/00621B01J 2219/0061B01J 2219/00531B01J 2219/00635B01J 2219/00612C07B 2200/11B01J 2219/00711C12Q 1/6834B01J 2219/00317C09D 4/00B01J 2219/00722B01J 2219/00637B01J 2219/00608C07H 21/00C07C 323/42C40B 60/14C07C 235/84B01J 2219/00619B01J 2219/00716C07C 45/63
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Abstract
Method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate. The reagent composition includes epoxide groups capable of covalently binding to the target molecule. Optionally, the composition can contain photoreactive groups for use in attaching the reagent composition to the surface. The reagent composition can be used to provide activated slides for use in preparing microarrays of nucleic acids.
Claims
exact text as granted — not AI-modified1 . A reagent composition for attaching a target molecule to the surface of a substrate, the reagent composition comprising a polymeric backbone adapted to be covalently attached to the surface and comprising one or more pendent epoxide groups adapted to form covalent bonds with corresponding functional groups on the target molecule.
2 . A reagent composition according to claim 1 wherein the reagent comprises a polymer formed by the polymerization of one or more monomers selected from the group glycidyl acrylate, glycidyl methacrylate, allylglycidyl ether, and glycidyl vinyl ether.
3 . A reagent composition according to claim 1 wherein the reagent comprises a polymer formed by the polymerization of one or more monomers of the formula:
where R 1 is either CH 3 or H and X is a noninterfering radical, preferably selected from the group:
where m=2-6 and n=1-10;
where n=1-10
—(CH 2 ) m —O—(CH 2 )—
where m=0 or 1; and
where m=1-20 and n=1-10.
4 . A reagent composition according to claim 1 wherein the reagent comprises a polymer synthesized by reacting hydroxyl- or amine-containing polymers with diepoxides.
5 . A reagent composition according to claim 1 wherein the target molecule comprises a nucleic acid and the surface comprises the surface of a support formed of organosilane-pretreated glass, organosilane-pretreated silicon, silicon hydride, or plastic.
6 . A reagent composition according to claim 5 wherein the nucleic acid comprises an underivatized nucleic acid.
7 . A reagent composition according to claim 6 wherein the underivatized nucleic acid comprises an oligonucleotide.
8 . A reagent composition according to claim 1 wherein the composition further comprises one or more latent reactive groups comprising photoreactive groups for covalently attaching the reagent composition to the surface upon application of energy from a suitable source.
9 . A reagent composition according to claim 8 wherein the target molecule is a nucleic acid and the photoreactive groups are selected from the group consisting of photoreactive aryl ketones.
10 . A reagent composition according to claim 1 wherein the polymeric backbone is selected from the group consisting of acrylics, vinyls, nylons, polyurethanes and polyethers, and the backbone further comprises one or more pendent photoreactive groups selected from the group consisting of aryl ketones.
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