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公开(公告)号:WO2023072448A1
公开(公告)日:2023-05-04
申请号:PCT/EP2022/071967
申请日:2022-08-04
Applicant: RESOLVE BIOSCIENCES GMBH
Inventor: KORFHAGE, Christian , FABER, Cynthia , MEIER, Andreas
IPC: C07H21/00 , C12Q1/68 , C12Q1/6834 , C12Q1/6837 , C12Q1/6858
Abstract: The technology provided herein relates to methods for of mounting/sticking a biological sample on a surface by contacting said biological sample on said surface with a reducing agent.
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公开(公告)号:WO2023059549A1
公开(公告)日:2023-04-13
申请号:PCT/US2022/045541
申请日:2022-10-03
Applicant: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Inventor: WOLLMAN, Roy
IPC: C12Q1/6813 , C12Q1/6832 , C12Q1/6834 , C12Q1/6886 , G01N29/24
Abstract: Methods for utilizing a nucleic acid-based multilevel perceptron are provided.
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公开(公告)号:WO2022256143A1
公开(公告)日:2022-12-08
申请号:PCT/US2022/028408
申请日:2022-05-10
Applicant: MICROSOFT TECHNOLOGY LICENSING, LLC
Inventor: CHEN, Yuan-Jyue , NGUYEN, Bichlien Hoang , STRAUSS, Karin , SMITH, Jake Allen
IPC: C12Q1/6806 , C12Q1/6823 , C12Q1/6834 , G16B50/00
Abstract: Electrode controlled hybridization is used to change local pH and selectively assemble oligonucleotide complexes on the surface of a microelectrode array. The oligonucleotide complexes have sticky ends that provide locations for subsequent oligonucleotide complexes to hybridize. The order in which specific oligonucleotide complexes are joined together encodes information. Controlled activation of individual electrodes in the microelectrode array creates negative voltages that reduces a buffer solution and raises the pH in proximity to the electrodes. At higher pH levels double-stranded oligonucleotides de-hybridize. Nicks between oligonucleotide complexes and oligonucleotides anchored to the microelectrode array are closed creating covalent attachments. De-hybridized single-stranded oligonucleotides are removed leaving only the oligonucleotides connected to microelectrode array. Thus, during a given round of synthesis, oligonucleotide complexes are added only to the locations on the microelectrode array where the electrodes are not activated.
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公开(公告)号:WO2022232027A1
公开(公告)日:2022-11-03
申请号:PCT/US2022/026147
申请日:2022-04-25
Applicant: MESO SCALE TECHNOLOGIES, LLC.
Inventor: KENTEN, John H. , NIKOLENKO, Galina
IPC: G01N33/50 , C12Q1/6834 , G01N33/573
Abstract: Described herein is a method of preparing a bifunctional assay surface. In particular, a method is provided for preparing an assay surface that includes a primary reagent and a secondary reagent. In one aspect, the primary and secondary reagents are immobilized on the assay surface by different surface chemistries. In one aspect, a method is provided for preparing an assay surface that includes a proteinaceous primary reagent and a thiol-containing secondary reagent. In one aspect, a method is provided for preparing an assay surface that includes a capture-target hybrid and a thiol-containing secondary reagent.
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公开(公告)号:WO2022173266A1
公开(公告)日:2022-08-18
申请号:PCT/KR2022/002185
申请日:2022-02-15
Applicant: 사회복지법인 삼성생명공익재단
IPC: B01L3/00 , C12Q1/6834 , C12Q1/6844
Abstract: 본 발명의 재조합 효소-중합효소 등온증폭 장치는 등온증폭을 실시함과 동시에 표면형광증폭이 일어나므로 민감도 및 특이도가 우수하며 소형화가 가능하므로 임상 현장의 병원체 진단에 이용될 수 있다.
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公开(公告)号:WO2022165188A1
公开(公告)日:2022-08-04
申请号:PCT/US2022/014329
申请日:2022-01-28
Applicant: ILLUMINA, INC. , ILLUMINA CAMBRIDGE LIMITED
Inventor: WU, Yir-Shyuan , GORPE-YASAR, Filiz , KHURANA, Tarun Kuman , BOUTELL, Jonathan Mark
IPC: C12Q1/6806 , C12Q1/6834 , C12Q1/6844
Abstract: The disclosure relates to methods, compositions, and kits for improving seeding efficiency of flow cells with polynucleotides, and applications thereof, including for sequencing.
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公开(公告)号:WO2022147134A1
公开(公告)日:2022-07-07
申请号:PCT/US2021/065525
申请日:2021-12-29
Applicant: 10X GENOMICS, INC.
Inventor: MCDERMOTT, Geoffrey , PATTERSON, David Michael , PRICE, Andrew D. , RAMACHANDRAN IYER, Eswar Prasad , SCHNALL-LEVIN, Michael
IPC: B01J19/00 , C12Q1/6834
Abstract: Provided in some aspects are methods for light-controlled in situ surface patterning of a substrate. Compositions such as nucleic acid arrays produced by the methods are also disclosed. In some embodiments, provided herein is photocontrollable hybridization, where oligonucleotides with photo-caged bases prevent hybridization of complementary nucleic acid strands. Uncaging of the oligonucleotides allows hybridization and/or ligation of nucleic acid molecules at the exposed area. A large diversity of barcodes can be created in molecules on the substrate via sequential rounds of light exposure, hybridization, and ligation.
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公开(公告)号:WO2022147005A1
公开(公告)日:2022-07-07
申请号:PCT/US2021/065340
申请日:2021-12-28
Applicant: 10X GENOMICS, INC.
Inventor: LUNDEBERG, Joakim , VILLACAMPA, Eva Gracia
IPC: C12Q1/6834
Abstract: Provided herein are methods and kits for determining the optimal conditions for analyte capture in biological samples.
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公开(公告)号:WO2022139292A1
公开(公告)日:2022-06-30
申请号:PCT/KR2021/018869
申请日:2021-12-13
Applicant: 에스에프씨 주식회사
IPC: C09K11/06 , C09B67/00 , C12Q1/6818 , C12Q1/6834
Abstract: 본 발명은 DNA를 포함한 핵산의 표지가 가능함과 동시에 들뜬 에너지 준위에서 발광 특성을 나타내는 형광성 리포터 및 이의 다양한 용도에 관한 것이다.
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公开(公告)号:WO2022060728A1
公开(公告)日:2022-03-24
申请号:PCT/US2021/050262
申请日:2021-09-14
Applicant: PALAMEDRIX, INC.
Inventor: GOPINATH, Ashwin , ROTHEMUND, Paul , SHETTY, Rishabh , BOWEN, Shane
IPC: B82Y5/00 , B82Y40/00 , C12Q1/6834 , G01N33/487 , G01N33/543
Abstract: Provided herein are structures and methods for detecting one or more analyte molecules present in a sample. In some embodiments, the one or more analyte molecules are detected using one or more supramolecular structures. In some embodiments, the one or more supramolecular structures are specifically designed to minimize cross-reactivity with each other. In some embodiments, the supramolecular structures are bi-stable, wherein the supramolecular structures shift from an unstable state to a stable state through interaction with one or more analyte molecules from the sample. In some embodiments, the stable state supramolecular structures are configured to provide a signal for analyte molecule detection and quantification. In some embodiments, the signal correlates to a DNA signal, such that detection and quantification of an analyte molecule comprises converting the presence of the analyte molecule into a DNA signal.
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