Array compositions and methods of making same
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C12Q-001/68
C12M-001/00
G01N-015/06
출원번호
US-0931271
(2001-08-16)
발명자
/ 주소
Dickinson, Todd
Coblentz, Kenneth D.
Carlson, Edward
출원인 / 주소
Illumina, Inc.
대리인 / 주소
Knobbe, Martens, Olson & Bear LLP
인용정보
피인용 횟수 :
77인용 특허 :
64
초록▼
The invention relates to sensor compositions comprising a composite array of individual arrays, to allow for simultaneous processing of a number of samples. The invention further provides methods of making and using the composite arrays. The invention further provides a hybridization chamber for use
The invention relates to sensor compositions comprising a composite array of individual arrays, to allow for simultaneous processing of a number of samples. The invention further provides methods of making and using the composite arrays. The invention further provides a hybridization chamber for use with a composite array.
대표청구항▼
1. An array composition comprising:(a) a rigid support;(b) a molded layer with at least a first assay location comprising discrete sites, wherein each of said discrete sites is configured to hold a single microsphere, and wherein said molded layer is adhered to said rigid support;(c) an adhesive lay
1. An array composition comprising:(a) a rigid support;(b) a molded layer with at least a first assay location comprising discrete sites, wherein each of said discrete sites is configured to hold a single microsphere, and wherein said molded layer is adhered to said rigid support;(c) an adhesive layer disposed between said rigid support and said molded layer; and(d) a population of microspheres comprising at least a first and a second subpopulation, wherein said first subpopulation comprises a first bioactive agent and said second subpopulation comprises a second bioactive agent wherein said microspheres are randomly distributed on said sites. 2. An array composition according to claim 1, wherein said sites are separated by a distance of at least about 5 μm. 3. An array composition according to claim 1, wherein said sites are separated by a distance of at most about 100 μm. 4. An array composition according to claim 1, wherein said rigid support is formatted to the dimensions of a microscope slide. 5. An array composition according to claim 1, wherein said molded layer comprises at least a second assay location comprising discrete sites. 6. An array composition according to claim 5, wherein said first and second assay locations are separated by a fluid barrier. 7. An array composition according to claim 6, wherein said fluid barrier is a physical fluid barrier. 8. An array composition according to claim 7, wherein said physical fluid barrier comprises a material that is added to said molded layer. 9. An array composition according to claim 8, wherein said molded layer comprises said physical fluid barrier. 10. An array composition according to claim 6, wherein said fluid barrier comprises a physico-chemical surface coating. 11. An array composition according to claim 1, wherein said first and second bioactive agents comprise nucleic acids. 12. An array composition according to claim 1, wherein said first and second bioactive agents comprise proteins. 13. A method for making an array composition containing at least a first assay location having discrete sites comprising the steps of:(a) contacting a surface of a template structure, said surface comprising one or more sets of projections, with a moldable material;(b) removing said moldable material from said surface of said template structure, whereby said removed moldable material forms a molded layer with at least a first assay location comprising discrete sites, wherein each of said discrete sites is configured to hold a single microsphere;(c) applying a layer of adhesive to adhere said molded layer to a rigid support in order to maintain the molded layer in a planar configuration; and(d) randomly distributing microspheres on said molded layer such that individual discrete sites comprise microspheres, wherein said microspheres comprise at least a first and a second subpopulation, wherein said first subpopulation comprises a first bioactive agent and said second subpopulation comprises a second bioactive agent. 14. The method according to claim 13, wherein the projections in said one or more sets of projections are separated by a distance of at least about 5 μm. 15. The method according to claim 13, wherein the projections in said one or more sets of projections are separated by a distance of at most about 100 μm. 16. The method according to claim 13, wherein said template structure is cylindrical, and steps (a) and (b) are carried out by a continuous process of rolling said cylindrical template structure wherein at a first portion of the cylinder, the cylinder is contacted with a moldable material and at a second portion of the cylinder, solidified moldable material is removed from the cylinder as a molded layer. 17. The method according to claim 13, wherein said molded layer is flexible. 18. The method according to claim 17, wherein prior to step (c), said flexible molded layer is stored in rolled form. 19. The method according to claim 13, wherein s aid molded layer comprises at least a second assay location comprising discrete sites. 20. The method according to claim 19, wherein said first and second assay locations are separated by a fluid barrier. 21. The method according to claim 19, further comprising the step of adding a fluid barrier to said molded layer, which fluid barrier separates said first and second assay locations. 22. The method according to claim 13, wherein said rigid support is formatted to at least one dimension of a microscope slide. 23. The method according to claim 13, further comprising a step of applying a releasing agent to said surface of said template structure prior to said contacting step. 24. The method according to claim 13, further comprising the step of coating the back surface of said molded layer with an adhering agent. 25. An array composition comprising:(a) a molded layer having an upper surface and a planar lower surface, wherein said upper surface comprises a first assay location comprising discrete sites, each of which is configured to hold a single microsphere;(b) a rigid support adhered to said planar lower surface and adapted to maintain said molded layer in a planar configuration; and(c) a population of microspheres comprising at least a first and a second subpopulation, wherein said first subpopulation comprises a first bioactive agent and said second subpopulation comprises a second bioactive agent, and wherein said microspheres are randomly distributed on said sites. 26. An array composition according to claim 25, wherein said sites are separated by a distance of at least about 5 μm. 27. An array composition according to claim 25, wherein said sites are separated by a distance of at most about 100 μm. 28. An array composition according to claim 25, wherein said molded layer comprises at least a second assay location comprising discrete sites. 29. An array composition according to claim 28, wherein said first and second assay locations are separated by a fluid barrier. 30. An array composition according to claim 29, wherein said fluid barrier is a physical fluid barrier. 31. An array composition according to claim 30, wherein said physical fluid barrier comprises a material that is added to said molded layer. 32. An array composition according to claim 31, wherein said molded layer comprises said physical fluid barrier. 33. An array composition according to claim 29, wherein said fluid barrier comprises a physico-chemical surface coating. 34. An array composition according to claim 25, wherein said first and second bioactive agents comprise nucleic acids. 35. An array composition according to claim 25, wherein said first and second bioactive agents comprise proteins. 36. An array composition according to claim 25, wherein said moldable layer is between 50 μm-1 mm in thickness. 37. An array composition according to claim 25, wherein said moldable layer is approximately 1 mm in thickness. 38. An array composition according to claim 25, wherein the rigid structure has optical properties. 39. An array composition according to claim 38, wherein the optical properties are selected from the group consisting of: having low autofluorescence, being transparent, being selectively transparent, being absorptive, being selectively absorptive, being opaque and being reflective. 40. An array composition according to claim 25, wherein the rigid support is composed of a material selected from the group consisting of: aluminum, iron, steel, an alloy, a ceramic, fiberglass, silicon, semiconductor materials, glass, rigid plastics, and rigid polymers.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (64)
Walt David R. (Lexington MA), Absorbance modulated fluorescence detection methods and sensors.
Honda Mitsuru (Tokyo JPX) Kawamura Takahisa (Yokohama JPX) Koike Atsushi (Chiba JPX) Murai Keiichi (Kashiwa JPX), Apparatus for producing a substrate having a surface with a plurality of spherical dimples for photoconductive members.
Ekins Roger P. (Department of Molecular Endocrinology University College and Middlesex School of Medicine Mortimer Street London W1N 8AA GBX) Chu Frederick W. (Department of Molecular Endocrinology U, Binding assay employing labelled reagent.
Still W. Clark (Clinton NY) Wigler Michael H. (Lloyd Harbor NY) Ohlmeyer Michael H. J. (Plainsboro NJ) Dillard Lawrence W. (Plainsboro NJ) Reader John C. (Princeton NJ), Complex combinatorial chemical libraries encoded with tags.
Goodman Barry D. (Baldwin NY) Wynne James J. (Mount Kisco NY) Kaufman Hershall W. (Setauket NY) Jacobs Jason M. (Baldwin NY), Dental procedures and apparatus using ultraviolet radiation.
Barany Francis ; Lubin Matthew ; Belgrader Phillip, Detection of nucleic acid sequence differences using coupled ligase detection and polymerase chain reactions.
Sutton Richard C. (Rochester NY) Ponticello Ignazio S. (Pittsford NY) Cummins Thomas J. (Rochester NY) Zander Dennis R. (Penfield NY) Donish William H. (Rochester NY), Element and method for nucleic acid amplification and detection using adhered probes.
Walt, David R.; Barnard, Steven M., Fiber optic array sensors, apparatus, and methods for concurrently visualizing and chemically detecting multiple analytes of interest in a fluid sample.
Gerdt David W. (P.O. Box 8175 Charlottesville VA 22906) Herr John C. (P.O. Box 8175 Charlottesville VA 22906), Fiber optic evanscent wave sensor for immunoassay.
Walt David R. (Lexington MA) Bernard Steven M. (Basel CHX), Fiber optic sensor, apparatus, and methods for detecting an organic analyte in a fluid or vapor sample.
Walt David R. (Lexington MA), Fiber optic sensors, apparatus, and detection methods using controlled release polymers and reagent formulations held wi.
Walt David R. (Lexington MA), Fiber optic sensors, apparatus, and detection methods using fluid erodible controlled release polymers for delivery of r.
Walt David R. (Lexington MA) Barnard Steven M. (Medford MA), Imaging fiber optic array sensors, apparatus, and methods for concurrently detecting multiple analytes of interest in a.
Nikiforov Theo (Baltimore MD) Karn Jonathan (Little Shelord GBX) Goelet Philip (Cockeysville MD), Ligase/polymerase mediated genetic bit analysis of single nucleotide polymorphisms and its use in genetic analysis.
Stabile Paul J. ; Ludington David Norman ; York Pamela Kay ; Rosen Arye ; Cherukuri Satyam Choudary ; Zanzucchi Peter John ; Heaney Paul, Massively parallel detection.
Seifert Kevin R. (Forest Lake MN) Lynch Laurie (Eden Prairie MN) Johnson Debra K. (Andover MN) Kalla Jonathan (St. Louis Park MN) Fowler William (Minneapolis MN), Method for manufacturing fiber optic sensors.
Sutton Richard Calvin ; Ponticello Ignazio Salvatore ; Cummins Thomas Joseph ; Zander Dennis Roland ; Donish William Harold ; Chen Paul Hong-Dze ; Findlay John Bruce, Method for nucleic acid amplification and detection using adhered probes.
Walt David R. (Lexington MA) Barnard Steven M. (Medford MA), Method of making imaging fiber optic sensors to concurrently detect multiple analytes of interest in a fluid sample.
Brown James F. ; Silver Jonathan E. ; Kalinina Olga V.,CAX, Method of sampling, amplifying and quantifying segment of nucleic acid, polymerase chain reaction assembly having nanoliter-sized sample chambers, and method of filling assembly.
Sosnowski Ronald G. ; Butler William F. ; Tu Eugene ; Nerenberg Michael I. ; Heller Michael J. ; Edman Carl F., Methods and procedures for molecular biological analysis and diagnostics.
Ishii Jennifer K. (San Diego CA) Ghosh Soumitra (San Diego CA), Non-isotopic detection of nucleic acids using a polystyrene support-based sandwich hybridization assay and compositions.
Walt David R. ; Michael Karri L ; Chadha Suneet, Optical sensor apparatus for far-field viewing and making optical analytical measurements at remote locations.
Walt David R. (Lexington MA) Kauer John S. (Weston MA), Optical sensor, optical sensing apparatus, and methods for detecting an analyte of interest using spectral recognition p.
Walt David R. (Lexington MA) Pantano Paul (Everett MA), Superresolution imaging fiber for subwavelength light energy generation and near-field optical microscopy.
Dower William J. (Menlo Park CA) Barrett Ronald W. (Sunnyvale CA) Gallop Mark A. (Palo Alto CA) Needels Michael C. (Oakland CA), Synthesizing and screening molecular diversity.
Barany Francis ; Zebala John ; Nickerson Deborah ; Kaiser ; Jr. Robert J. ; Hood Leroy, Thermostable ligase mediated DNA amplification system for the detection of genetic diseases.
Barany Francis ; Zebala John ; Nickerson Deborah ; Kaiser ; Jr. Robert J. ; Hood Leroy, Thermostable ligase mediated DNA amplification system for the detection of genetic diseases.
Barany Francis (New York NY) Zebala John (New York NY) Nickerson Deborah (Seattle WA) Kaiser ; Jr. Robert J. (Seattle WA) Hood Leroy (Seattle WA), Thermostable ligase-mediated DNA amplifications system for the detection of genetic disease.
Walt David R. (Lexington MA) Bronk Karen S. (Somerville MA), Thin film fiber optic sensor array and apparatus for concurrent viewing and chemical sensing of a sample.
Testa, Gregory A.; Poulsen, Tim Svenstrup; Matthiesen, Steen Hauge; Rasmussen, Ole Feldballe; Winther, Lars, Apparatus and method for processing biological samples and a reservoir therefor.
Rothberg,Jonathan M.; Bader,Joel S.; Dewell,Scott B.; McDade,Keith; Simpson,John W.; Berka,Jan; Colangelo,Christopher M.; Weiner,Michael P., Apparatus and method for sequencing a nucleic acid.
Testa, Gregory A.; Poulsen, Tim Svenstrup; Matthiesen, Steen Hauge; Rasmussen, Ole Feldballe; Winther, Lars, Apparatus and methods for processing biological samples and a reservoir therefor.
Testa, Gregory A.; Poulsen, Tim Svenstrup; Matthiesen, Steen Hauge; Rasmussen, Ole Feldballe; Winther, Lars, Apparatus and methods for processing biological samples and a reservoir therefor.
Stuelpnagel, John R.; Chee, Mark S.; Auger, Steven R.; Wang, Gan G.; Casas, Laura S.; Baker, Shawn Christopher; Kain, Robert C., Array kits and processing systems.
Triener, Alexander; Allegoren, Erik; Feng, Wenyi; Buermann, Dale; Olson, Erik; Osmus, James, Assay instrument for detecting optical signals from samples having a controlled optics adjustment system based on the priority statuses of the samples.
Fuchs, Martin; Wang, Ying-Xin; Huang, Yi-Shuian; Krueger, Neil X., Devices and methods for enrichment and alteration of circulating tumor cells and other particles.
Rothberg,Jonathan M.; Bader,Joel S.; Dewell,Scott B.; McDade,Keith; Simpson,John W.; Berka,Jan; Colangelo,Christopher M., Method of sequencing a nucleic acid.
Rothberg,Jonathan M.; Bader,Joel S.; Dewell,Scott B.; McDade,Keith; Simpson,John W.; Berka,Jan; Colangelo,Christopher M., Method of sequencing a nucleic acid.
Rothberg,Jonathan M.; Bader,Joel S.; Dewell,Scott B.; McDade,Keith; Simpson,John W.; Berka,Jan; Colangelo,Christopher M., Method of sequencing a nucleic acid.
Lebl, Michal; Perbost, Michel; DeRosier, Chad F.; Nibbe, Mark J.; Burgett, Steve R.; Heiner, David L., Methods and compositions for processing chemical reactions.
Lebl, Michal; Perbost, Michel; Derosier, Chad F.; Nibbe, Mark J.; Burgett, Steve R.; Heiner, David L., Methods and compositions for processing chemical reactions.
Rawlings, Stephen; Rao, Venkatesh Mysore Nagaraja; Ang, Beng Keong; Udpa, Nitin, Methods, carrier assemblies, and systems for imaging samples for biological or chemical analysis.
Bowen, M. Shane; Gunderson, Kevin L.; Lin, Shengrong; Rogert Bacigalupo, Maria Candelaria; Vijayan, Kandaswamy; Wu, Yir-Shyuan; Venkatesan, Bala Murali; Tsay, James; Beierle, John M.; Berti, Lorenzo; Park, Sang Ryul, Microarray fabrication system and method.
Bowen, M. Shane; Gunderson, Kevin L.; Lin, Shengrong; Rogert Bacigalupo, Maria Candelaria; Vijayan, Kandaswamy; Wu, Yir-Shyuan; Venkatesan, Bala Murali; Tsay, James; Beierle, John M.; Berti, Lorenzo; Park, Sang Ryul, Microarray fabrication system and method.
Pacholski, Claudia; Miskelly, Gordon M.; Sailor, Michael J., Multiple superimposed interface pattern porous microstructure multi layer biosensing method.
Dubowski, Jan J.; Ding, Ximing; Frost, Eric H.; Escher, Emanuel, Quantum dot template for fast and simultaneous detection of different infectious agents.
Bedingham, William; Carter, Chad J.; Harkins, Robert A.; Harms, Michael R.; Kokaisel, Christopher R.; North, Diane; Wood, Kenneth B., Sample processing devices and carriers.
Seo, Sung-Min; Lee, Do-Bu; Lee, Joong Hwan; Paek, Mun-Cheol; Ku, Su-Jin, System for integrated analysis of real-time polymerase chain reaction and DNA chip and method for integrated analysis using the same.
Triener, Alexander; Allegoren, Erik; Feng, Wenyi; Buermann, Dale; Olson, Erik; Osmus, James, Systems, methods, and apparatuses including a moveable optical component for detecting optical signals from a sample.
Reed, Mark T.; Williamson, Eric; Crane, Bryan; Leung, Patrick; Buermann, Dale; Kindwall, Alexander P.; Erie, Frederick; Pratt, Mark; Harris, Jason; Carson, Andrew James; Hong, Stanley S.; Bryant, Jason; Wang, Mark; Verkade, Drew, Systems, methods, and apparatuses to image a sample for biological or chemical analysis.
Williamson, Erik; Crane, Bryan; Leung, Patrick; Verkade, Drew; Reed, Mark T., Systems, methods, and apparatuses to image a sample for biological or chemical analysis.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.