发明名称 Detection of single and multimodal analytes
摘要 A method for detecting analyte in a sample comprises: (a) contacting said sample with at least one set comprising a cassette oligonucleotide and first, second, third and fourth proximity probes, which probes each comprise an analyte-binding domain and a nucleic acid domain and can simultaneously bind to the analyte, the nucleic acid domains of said first and third proximity probes being complementary in a first overlap region and the nucleic acid domains of said second and fourth proximity probes being complementary in a second overlap region; andsaid cassette oligonucleotide being complementary to the nucleic acid domain of said third proximity probe in a third overlap region and to the nucleic acid domains of said fourth proximity probe in a fourth overlap region;(b) allowing the overlap regions of said proximity probes and said cassette oligonucleotide to hybridise; and(c) detecting said hybridisation.;A kit is for performing the method.
申请公布号 US9029086(B2) 申请公布日期 2015.05.12
申请号 US201213612002 申请日期 2012.09.12
申请人 发明人 Moghaddam Masood Kamali
分类号 C12Q1/68;C07H21/04;G01N33/53 主分类号 C12Q1/68
代理机构 Porter Wright Morris & Arthur LLP 代理人 Porter Wright Morris & Arthur LLP
主权项 1. A method for detecting an analyte in a sample, wherein the analyte can simultaneously bind four analyte-binding domains, comprising: (a) contacting said sample with at least one set comprising a cassette oligonucleotide and first, second, third and fourth proximity probes, which probes each comprise an analyte-binding domain and a nucleic acid domain, wherein the respective analyte-binding domains simultaneously bind to the analyte; wherein the nucleic acid domains of said first and said third proximity probes include respective first overlapping regions which are complementary and can hybridize and the nucleic acid domains of said second and said fourth proximity probes include respective second overlapping regions which are complementary and can hybridize; and wherein said cassette oligonucleotide and the nucleic acid domain of said third proximity probe include respective third overlapping regions which are complementary and can hybridize, and said cassette oligonucleotide and the nucleic acid domain of said fourth proximity probe include respective fourth overlapping regions which are complementary and can hybridize; (b) hybridising the respective overlapping regions of said proximity probes and said cassette oligonucleotide; and (c) detecting the analyte in the sample based on detecting a hybridization product of step (b).
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