发明名称 Processes for detecting or quantifying nucleic acids using an array of fixed or immobilized nucleic acids
摘要 This invention provides novel compositions and processes for analyte detection, quantification and amplification. Nucleic acid arrays and libraries of analytes are usefully incorporated into such compositions and processes. Universal detection elements, signaling entities and the like are employed to detect and if necessary or desirable, to quantify analytes. Amplification of target analytes are also provided by the compositions and processes of this invention.
申请公布号 US9617584(B2) 申请公布日期 2017.04.11
申请号 US201514812293 申请日期 2015.07.29
申请人 Enzo Biochem, Inc. 发明人 Rabbani Elazar;Stavrianopoulos Jannis G.;Donegan James J.;Coleman Jack
分类号 C12P19/34;C12Q1/68;C07H21/00;C12N15/10;B01J19/00;C40B40/00 主分类号 C12P19/34
代理机构 代理人 Diamond, Esq. Paul
主权项 1. A process for detecting or quantifying more than one nucleic acid of interest in a library comprising the steps of: a) providing: (i) an array of fixed or immobilized nucleic acids identical or complementary in part or whole to sequences of said nucleic acids of interest;(ii) a library of nucleic acid analytes which may contain the nucleic acids of interest sought to be detected or quantified;(iii) a first set of primers and a second set of primers, wherein the first set of primers comprises at least one production center;(iv) polymerizing means for synthesizing nucleic acid copies of said nucleic acid analytes using the first set of primers and the second set of primers;(v) a set of oligonucleotides or polynucleotides complementary to at least one segment or sequence of said second set of primers;(vi) ligating means for ligating said set of oligonucleotides or polynucleotides (v); and(vii) synthesizing means for synthesizing nucleic acid copies under isothermal or isostatic conditions from a production center; b) contacting said library of nucleic acid analytes with said first set of primers to form more than one first bound entity, each comprising a first set primer hybridized to a nucleic acid analyte; c) using said polymerizing means, extending said bound first set primers of the first bound entities using said nucleic acid analytes of the first bound entities as templates to form first copies of said analytes; d) using said ligating means, ligating said set of oligonucleotides or polynucleotides a)(v) to the 3′ end of said first copies formed in step c) to form more than one ligated product; e) contacting said ligated products with said second set of primers to form more than one second bound entity, each comprising a second set primer hybridize to one of the ligated products; f) using said polymerizing means, extending said bound second set primers of the second bound entities using said ligated products of the second bound entities as templates to form more than one complex comprising said ligated products and said extended second set primers; g) using said synthesizing means, synthesizing under isothermal or isostatic conditions from a production center in said first set of primers incorporated in said complexes one or more nucleic acid copies; h) hybridizing said nucleic acid copies formed in step g) to said array of nucleic acids provided in step a) (i); and i) detecting or quantifying any of said hybridized copies obtained in step h).
地址 New York NY US