CA3084920C - Methods for isolating microvesicles and extracting nucleic acids from biological samples - Google Patents
Methods for isolating microvesicles and extracting nucleic acids from biological samples Download PDFInfo
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- CA3084920C CA3084920C CA3084920A CA3084920A CA3084920C CA 3084920 C CA3084920 C CA 3084920C CA 3084920 A CA3084920 A CA 3084920A CA 3084920 A CA3084920 A CA 3084920A CA 3084920 C CA3084920 C CA 3084920C
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- C12N15/1006—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers
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| AU2012253366A1 (en) * | 2011-05-11 | 2014-01-09 | Exosome Diagnostics, Inc. | Nucleic acid extraction from heterogeneous biological materials |
| US11268085B2 (en) | 2014-05-27 | 2022-03-08 | Exosome Diagnostics, Inc. | Methods for isolating microvesicles and extracting nucleic acids from biological samples |
| AU2015287763B2 (en) | 2014-07-09 | 2019-08-08 | Exosome Diagnostics, Inc. | Methods for isolating microvesicles and extracting nucleic acids from biological samples |
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| EP3443117A1 (en) | 2016-04-15 | 2019-02-20 | Exosome Diagnostics, Inc. | Plasma-based detection of anaplastic lymphoma kinase (alk) nucleic acids and alk fusion transcripts and uses thereof in diagnosis and treatment of cancer |
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| ES2908932T3 (es) | 2016-05-05 | 2022-05-04 | Exosome Diagnostics Inc | Perfilado de ácidos nucleicos de microvesícula y usos del mismo como características distintivas en diagnóstico de rechazo de trasplante renal |
| US10808240B2 (en) * | 2016-05-13 | 2020-10-20 | Exosome Diagnostics, Inc. | Automated and manual methods for isolation of extracellular vesicles and co-isolation of cell-free DNA from biofluids |
| AU2017313138B2 (en) | 2016-08-17 | 2024-01-04 | The Regents Of The University Of California | A novel immunoprobe-based method to assess organ injury status through a biofluid-based cell-free DNA (cfDNA) assay |
| WO2018052011A1 (ja) | 2016-09-14 | 2018-03-22 | 東レ株式会社 | セルフリーｄｎａの回収方法 |
| WO2018076018A1 (en) | 2016-10-21 | 2018-04-26 | Exosome Diagnostics, Inc. | Sequencing and analysis of exosome associated nucleic acids |
| CA3044056A1 (en) | 2016-11-30 | 2018-06-07 | Exosome Diagnostics, Inc. | Methods and compositions to detect mutations in plasma using exosomal rna and cell free dna from non-small cell lung cancer patients |
| KR20190100174A (ko) * | 2016-12-23 | 2019-08-28 | 엑소팜 리미티드 | 미세소포 및 엑소좀의 정제 또는 단리를 위한 방법 및 조성물 |
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| CA3048212A1 (en) * | 2017-01-06 | 2018-07-12 | Mantra Bio, Inc. | Systems and methods for algorithmic extracellular vesicle population discovery and characterization |
| KR101875594B1 (ko) * | 2017-01-13 | 2018-07-06 | ㈜로제타엑소좀 | 금속을 이용한 세포밖 소포체의 분리 방법 |
| GB201706680D0 (en) * | 2017-04-27 | 2017-06-14 | Ge Healthcare Uk Ltd | Device and method for sample isolation |
| EP3635139A1 (en) | 2017-05-17 | 2020-04-15 | Exosome Diagnostics, Inc. | Microvesicle nucleic acids and/or proteins and uses thereof as markers of renal transplant rejection |
| CN107267440A (zh) * | 2017-06-09 | 2017-10-20 | 李刚 | 适用于外泌体提取的提取试剂及应用及其提取方法 |
| EP3652315A4 (en) | 2017-07-12 | 2021-09-01 | Exosome Diagnostics, Inc. | METHODS FOR ISOLATION AND ENRICHMENT OF EXTRACELLULAR VESICLE POPULATIONS DERIVED FROM BIOFLUIDS, AND ASSOCIATED METHODS OF USE |
| US11390864B2 (en) | 2017-07-12 | 2022-07-19 | Illumina, Inc. | Nucleic acid extraction materials, systems, and methods |
| WO2019018537A1 (en) * | 2017-07-18 | 2019-01-24 | Exosome Diagnostics, Inc. | NUCLEIC ACID SEQUENCING ASSOCIATED WITH EXOSOMAL ISOLATION IN PATIENTS WITH MULTIPLE GLIOBLASTOMA |
| CN111148828A (zh) * | 2017-07-26 | 2020-05-12 | 罗塞塔外排体株式会社 | 利用阳离子分离细胞外囊泡的方法 |
| WO2019060369A1 (en) * | 2017-09-20 | 2019-03-28 | Molecular Stethoscope, Inc. | METHODS AND SYSTEMS FOR DETECTION OF TISSUE DISORDERS |
| WO2019089836A1 (en) | 2017-10-31 | 2019-05-09 | Encodia, Inc. | Kits for analysis using nucleic acid encoding and/or label |
| US11260347B2 (en) * | 2017-12-26 | 2022-03-01 | Limited Liability Company “Prostagnost” | Method and device for separating extracellular vesicles from biological liquids with the aid of cascade ultrafiltration |
| WO2019164227A1 (ko) * | 2018-02-20 | 2019-08-29 | 고려대학교 산학협력단 | 엑소좀을 분리하기 위한 다중 컬럼 및 엑소좀 분리 방법 |
| WO2019236853A1 (en) | 2018-06-06 | 2019-12-12 | Exosome Diagnostics, Inc. | Methods for developing urine biomarkers and for detecting bladder cancer |
| EP3807616A4 (en) | 2018-06-18 | 2022-03-23 | Exopharm Limited | METHODS AND COMPOSITIONS FOR PURIFICATION OR ISOLATION OF MICROVESICLES AND EXOSOMES |
| CN108841777A (zh) * | 2018-06-22 | 2018-11-20 | 北京恩泽康泰生物科技有限公司 | 基于静电吸附的胞外囊泡及其内含物的提取方法及装置 |
| JP7426725B2 (ja) * | 2018-10-30 | 2024-02-02 | Ｃｒａｉｆ株式会社 | 細胞外小胞を捕捉するために用いられるデバイス、細胞外小胞の保存方法および移送方法 |
| WO2020106853A1 (en) | 2018-11-20 | 2020-05-28 | Exosome Diagnostics, Inc. | Compositions and methods for internal controls of microvesicle isolations |
| CN114072499B (zh) | 2019-04-30 | 2024-08-06 | Encodia公司 | 用于制备分析物的方法和相关试剂盒 |
| EP4010488A1 (en) * | 2019-08-08 | 2022-06-15 | Biocartis NV | Novel nucleic acid purification chemistry |
| EP4031865A2 (en) | 2019-09-18 | 2022-07-27 | Exosome Diagnostics, Inc. | Compositions, methods, and kits for the isolation of extracellular vesicles |
| WO2021089606A1 (en) * | 2019-11-04 | 2021-05-14 | Nasasbiotech, S.L. | Method for isolating nucleic acids |
| EP4077659A1 (en) * | 2019-12-16 | 2022-10-26 | QIAGEN GmbH | Enrichment method |
| EP4077660A1 (en) * | 2019-12-16 | 2022-10-26 | QIAGEN GmbH | Method for enriching vesicular rna |
| WO2021215539A1 (ja) * | 2020-04-24 | 2021-10-28 | 東洋紡株式会社 | イオン交換膜 |
| WO2021215878A1 (ko) * | 2020-04-24 | 2021-10-28 | 고려대학교 산학협력단 | 미세소포체 분리방법 및 미세소포체 분리장치 |
| US20230203587A1 (en) | 2020-05-29 | 2023-06-29 | Exosome Diagnostics, Inc. | Use of microvesicle signature for the diagnosis and treatment of kidney transplant rejection |
| EP4263383A4 (en) | 2020-12-17 | 2024-10-23 | Nephrosant, Inc. | KITS FOR STABILIZATION OF URINE SAMPLES |
| WO2022263500A1 (en) * | 2021-06-17 | 2022-12-22 | Qiagen Gmbh | Method for isolating non-vesicular mirna |
| US20250075258A1 (en) | 2021-07-16 | 2025-03-06 | Exosome Diagnostics, Inc. | Methods of detecting sjogren's syndrome using salivary exosomes |
| DE102021208893B3 (de) | 2021-08-13 | 2022-11-17 | Hahn-Schickard-Gesellschaft für angewandte Forschung e.V. | Isolieren von Analyten unterschiedlicher Analyt-Klassen |
| EP4419911A4 (en) * | 2021-10-28 | 2025-03-05 | 10X Genomics, Inc. | Methods for sample preparation |
| AU2023221644A1 (en) | 2022-02-18 | 2024-09-12 | Bio-Techne Corporation | Use of microvesicle signatures in the identification and treatment of renal disorders |
| WO2024054572A1 (en) | 2022-09-07 | 2024-03-14 | Exosome Diagnostics, Inc. | Methods of detecting sjögren's syndrome using salivary exosomes |
| CN115960885B (zh) * | 2022-10-09 | 2023-12-12 | 南京诺唯赞生物科技股份有限公司 | 一种提取肝素钠样品中核酸的方法及组合物 |
| KR102784335B1 (ko) * | 2023-02-09 | 2025-03-19 | 순천향대학교 산학협력단 | 세포유리핵산의 고농축화 분리 방법 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4935342A (en) | 1986-12-01 | 1990-06-19 | Syngene, Inc. | Method of isolating and purifying nucleic acids from biological samples |
| US5438128A (en) | 1992-02-07 | 1995-08-01 | Millipore Corporation | Method for rapid purifiction of nucleic acids using layered ion-exchange membranes |
| US5639606A (en) | 1993-04-06 | 1997-06-17 | The University Of Rochester | Method for quantitative measurement of gene expression using multiplex competitive reverse transcriptase-polymerase chain reaction |
| AU689815B2 (en) * | 1993-08-30 | 1998-04-09 | Promega Corporation | Nucleic acid purification compositions and methods |
| FR2788780B1 (fr) * | 1999-01-27 | 2001-03-30 | Ap Cells Inc | Procede de preparation de vesicules membranaires |
| GB9927320D0 (en) | 1999-11-18 | 2000-01-12 | Chiron Spa | Exosome separation |
| US6812023B1 (en) | 2000-04-27 | 2004-11-02 | Anosys, Inc. | Methods of producing membrane vesicles |
| WO2008045505A2 (en) * | 2006-10-10 | 2008-04-17 | Xenomics, Inc. | Compositions, methods and kits for isolating nucleic acids from body fluids using anion exchange media |
| EP2245199B1 (en) | 2008-02-01 | 2013-11-13 | The General Hospital Corporation | Use of microvesicles in diagnosis, prognosis and treatment of medical diseases and conditions |
| WO2010065765A2 (en) * | 2008-12-04 | 2010-06-10 | Aethlon Medical, Inc. | Affinity capture of circulating biomarkers |
| WO2010141862A2 (en) * | 2009-06-05 | 2010-12-09 | Mayo Foundation For Medical Education And Research | Methods and materials for isolating exosomes |
| US20130158247A1 (en) | 2010-06-01 | 2013-06-20 | Qiagen Gmbh | Method for isolating and/or purifying nucleic acid(s) |
| WO2012006476A2 (en) * | 2010-07-07 | 2012-01-12 | Aethlon Medical, Inc. | Methods and compositions for quantifying exosomes |
| US8945509B2 (en) * | 2010-08-20 | 2015-02-03 | Life Technologies Corporation | Magnetic beads having surface glycoconjugates and use thereof |
| WO2012064993A1 (en) * | 2010-11-10 | 2012-05-18 | Exosome Diagnosties, Inc. | Method for isolation of nucleic acid containing particles and extraction of nucleic acids therefrom |
| SG190450A1 (en) * | 2010-12-20 | 2013-06-28 | Agency Science Tech & Res | Method of purifying exosomes |
| AU2012253366A1 (en) * | 2011-05-11 | 2014-01-09 | Exosome Diagnostics, Inc. | Nucleic acid extraction from heterogeneous biological materials |
| BR112013032232A2 (pt) * | 2011-06-16 | 2016-09-20 | Caris Life Sciences Switzerland Holdings S A R L | método de caracterização de câncer através do uso de biomarcador de ácido nucleico |
| KR20140005688A (ko) * | 2012-07-06 | 2014-01-15 | 삼성전자주식회사 | 사용자 인터페이스 방법 및 장치 |
| US11136627B2 (en) | 2012-08-30 | 2021-10-05 | Exosome Diagnostics, Inc. | Controls for nucleic acid assays |
| KR101933621B1 (ko) * | 2012-09-28 | 2018-12-28 | 삼성전자주식회사 | 소포를 분리하기 위한 조성물, 키트 및 이를 이용하여 소포를 분리하는 방법 |
| MX392552B (es) | 2013-01-03 | 2025-03-11 | Exosome Diagnostics Inc | Métodos para aislar microvesículas. |
| AU2015287763B2 (en) | 2014-07-09 | 2019-08-08 | Exosome Diagnostics, Inc. | Methods for isolating microvesicles and extracting nucleic acids from biological samples |
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