The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Apr. 05, 2016

Filed:

Jun. 10, 2013
Applicants:

The Regents of the University of Michigan, Ann Arbor, MI (US);

University of Houston, Houston, TX (US);

Inventors:

Xiaolian Gao, Houston, TX (US);

Hua Zhang, Houston, TX (US);

Peillin Yu, Houston, TX (US);

Eric Leproust, Campbell, CA (US);

Jean Philippe Pellois, New York, NY (US);

Qin Xiang, Houston, TX (US);

Xiaochuan Zhou, Houston, TX (US);

Assignees:

THE REGENTS OF THE UNIVERSITY OF MICHIGAN, Ann Arbor, MI (US);

UNIVERSITY OF HOUSTON, Houston, TX (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C40B 40/06 (2006.01); C40B 50/14 (2006.01); C40B 50/18 (2006.01); C07H 21/00 (2006.01); C07H 19/06 (2006.01); C07H 21/02 (2006.01);
U.S. Cl.
CPC ...
C07H 19/06 (2013.01);
Abstract

A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.


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