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:
Feb. 27, 2018

Filed:

Oct. 25, 2012
Applicants:

Helmholtz-zentrum Fuer Umweltforschung Gmbh—ufz, Leipzig, DE;

Albert-ludwigs-universitaet Freiburg, Freiburg im Breisgau, DE;

Inventors:

Guenter Roth, Freiburg im Breisgau, DE;

Christine Reinemann, Leipzig, DE;

Beate Strehlitz, Leipzig, DE;

Assignee:

Albert-Ludwigs-Universitaet Freiburg, Freiburg im Breisgau, DE;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/68 (2006.01); C07H 21/02 (2006.01); C07H 21/04 (2006.01); G01N 33/53 (2006.01); C12N 15/10 (2006.01); C12N 5/00 (2006.01);
U.S. Cl.
CPC ...
G01N 33/5308 (2013.01); C12N 15/1048 (2013.01); C12Q 1/6811 (2013.01);
Abstract

The invention relates to a method for identifying aptamers, having the following steps —bringing a mixture of oligonucleotides into contact with an aptamer target structure and binding at least some of the oligonucleotides to the target structure, —separating the oligonucleotides which have been bound to the aptamer target structure from the aptamer target structure and from oligonucleotides that are not bound to the aptamer target structure, —amplifying individual oligonucleotides which were bound to the aptamer target structure in a physically separate manner and producing a plurality of physically separate amplicons, each amplicon predominantly containing one type of oligonucleotides, —specifying a specific marker for a plurality of the physically separate amplicons such that each of the marked amplicons can be uniquely identified using the specified marker of the amplicon, —sequencing oligonucleotides in a plurality of marked amplicons and assigning the marker that is specific for the amplicon to the sequence of the type of oligonucleotides in the amplicon for each amplicon examined by means of the sequencing process —analyzing the binding properties of the types of oligonucleotides to the aptamer target structure and assigning the analyzed binding properties to the specific markers of the amplicons and to the sequences of the types of oligonucleotides.


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