Invention Grant
- Patent Title: Exonuclease enabled proximity extension assays
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Application No.: US13981943Application Date: 2012-01-30
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Publication No.: US09777315B2Publication Date: 2017-10-03
- Inventor: Simon Fredriksson , Martin Lundberg , Anna Eriksson , Emma Rennel-Dickens
- Applicant: Simon Fredriksson , Martin Lundberg , Anna Eriksson , Emma Rennel-Dickens
- Applicant Address: SE Uppsala
- Assignee: OLINK PROTEOMICS AB
- Current Assignee: OLINK PROTEOMICS AB
- Current Assignee Address: SE Uppsala
- Agency: Porter Wright Morris & Arthur
- Priority: GB1101621.9 20110131
- International Application: PCT/EP2012/051474 WO 20120130
- International Announcement: WO2012/104261 WO 20120809
- Main IPC: C12Q1/68
- IPC: C12Q1/68 ; C12P19/34 ; G01N33/542 ; G01N33/558

Abstract:
The present invention relates to a proximity probe based detection assay (“proximity assay”) for an analyte in a sample, specifically a proximity probe extension assay (PEA), an in particular to an improvement in the method to reduce non-specific “background” signals, wherein the improvement comprises the use in such assays of a component comprising 3′ exonuclease activity, said method comprising: (a) contacting said sample with at least one set of at least first and second proximity probes, which probes each comprise an analyte-binding domain and a nucleic acid domain and can simultaneously bind to the analyte; (b) allowing the nucleic acid domains of the proximity probes to interact with each other upon binding of said proximity probes to said analyte, wherein said interaction comprises the formation of a duplex; (c) contacting said sample with a component comprising 3′ exonuclease activity; (d) extending the 3′ end of at least one nucleic acid domain of said duplex to generate an extension product, wherein the step may occur contemporaneously with or after step (c); and (e) amplifying and detecting the extension product.
Public/Granted literature
- US20140030721A1 Exonuclease Enabled Proximity Extension Assays Public/Granted day:2014-01-30
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