WO1999041007A2 - Method and apparatus for chemical and biochemical reactions using photo-generated reagents - Google Patents
Method and apparatus for chemical and biochemical reactions using photo-generated reagents Download PDFInfo
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- WO1999041007A2 WO1999041007A2 PCT/US1999/002945 US9902945W WO9941007A2 WO 1999041007 A2 WO1999041007 A2 WO 1999041007A2 US 9902945 W US9902945 W US 9902945W WO 9941007 A2 WO9941007 A2 WO 9941007A2
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- C40B60/00—Apparatus specially adapted for use in combinatorial chemistry or with libraries
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- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
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JP2000531248A JP4503828B2 (ja) | 1998-02-11 | 1999-02-10 | 光生成試薬を用いる化学反応および生化学反応のための方法および装置 |
AT99906913T ATE246041T1 (de) | 1998-02-11 | 1999-02-10 | Vorrichtung zur durchführung chemischer und biochemischer reaktionen unter anwendung von photoerzeugten reagenzien |
EP99906913A EP1054726B1 (en) | 1998-02-11 | 1999-02-10 | Apparatus for chemical and biochemical reactions using photo-generated reagents |
AU26714/99A AU755239B2 (en) | 1998-02-11 | 1999-02-10 | Method and apparatus for chemical and biochemical reactions using photo-generated reagents |
CA002319587A CA2319587C (en) | 1998-02-11 | 1999-02-10 | Method and apparatus for chemical and biochemical reactions using photo-generated reagents |
DE69909972T DE69909972T2 (de) | 1998-02-11 | 1999-02-10 | Vorrichtung zur durchführung chemischer und biochemischer reaktionen unter anwendung von photoerzeugten reagenzien |
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Cited By (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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EP1066506A1 (en) * | 1998-02-23 | 2001-01-10 | Wisconsin Alumni Research Foundation | Method and apparatus for synthesis of arrays of dna probes |
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US6838447B2 (en) | 2001-03-26 | 2005-01-04 | Linden Technologies, Inc. | Particulate compositions for chemical synthesis |
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US6962822B2 (en) | 2002-08-07 | 2005-11-08 | International Business Machines Corporation | Discrete nano-textured structures in biomolecular arrays, and method of use |
WO2006117556A2 (en) * | 2005-05-04 | 2006-11-09 | The Institute Of Cancer Research: Royal Cancer Hospital | Materials and methods for the photodirected synthesis of oligonucleotide arrays |
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US7435575B2 (en) | 2000-12-28 | 2008-10-14 | Roche Molecular Systems, Inc. | Method for processing a nucleic acid sample by oscillating a cartridge, a system and a cartridge for performing such a method |
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US7862996B2 (en) | 2005-12-29 | 2011-01-04 | Affymetrix, Inc. | Use of acid scavengers for the synthesis of standard length and long-mer nucleic acid arrays |
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US8822158B2 (en) | 2009-02-25 | 2014-09-02 | Roche Molecular Systems, Inc. | Miniaturized, high-throughput nucleic acid analysis |
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Publication number | Priority date | Publication date | Assignee | Title |
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US20040115654A1 (en) * | 2002-12-16 | 2004-06-17 | Intel Corporation | Laser exposure of photosensitive masks for DNA microarray fabrication |
US7923550B2 (en) * | 2003-04-14 | 2011-04-12 | Xiaolian Gao | Reagent compounds and methods of making and using the same |
US7858387B2 (en) * | 2003-04-30 | 2010-12-28 | Perkinelmer Health Sciences, Inc. | Method of scanning a sample plate surface mask in an area adjacent to a conductive area using matrix-assisted laser desorption and ionization mass spectrometry |
KR100561842B1 (ko) | 2003-08-25 | 2006-03-16 | 삼성전자주식회사 | 단량체 광산발생제 조성물, 상기 조성물로 코팅된 기판,상기 단량체 광산발생제 조성물을 이용하여 기판상에서화합물을 합성하는 방법 및 상기 방법에 의하여 제조된마이크로어레이 |
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US20050272059A1 (en) * | 2004-02-12 | 2005-12-08 | Xiaolian Gao | Method for providing microarrays |
CA2557841A1 (en) * | 2004-02-27 | 2005-09-09 | President And Fellows Of Harvard College | Polony fluorescent in situ sequencing beads |
WO2005089110A2 (en) * | 2004-02-27 | 2005-09-29 | President And Fellows Of Harvard College | Polynucleotide synthesis |
US7435074B2 (en) * | 2004-03-13 | 2008-10-14 | International Business Machines Corporation | Method for fabricating dual damascence structures using photo-imprint lithography, methods for fabricating imprint lithography molds for dual damascene structures, materials for imprintable dielectrics and equipment for photo-imprint lithography used in dual damascence patterning |
US20050214779A1 (en) * | 2004-03-29 | 2005-09-29 | Peck Bill J | Methods for in situ generation of nucleic acid arrays |
DE102004019098A1 (de) | 2004-04-20 | 2005-11-10 | Chemogenix Gmbh | Photolabile Schutzgruppen |
DE102004056980A1 (de) * | 2004-11-25 | 2006-06-01 | Clondiag Chip Technologies Gmbh | Verfahren zur ortsspezifischen Synthese von Biopolymeren auf festen Trägern |
DE102004062256A1 (de) * | 2004-12-23 | 2006-07-13 | Basf Ag | Hochempfindliches Verfahren zur Detektion von Unterschieden zwischen den physikalisch messbaren Eigenschaften einer Probe und einer Referenz |
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US20090023609A1 (en) * | 2005-12-08 | 2009-01-22 | Moon Youn Jung | Programmable mask for fabricating biomolecule array or polymer array, apparatus for fabricating biomolecule array or polymer array including the programmable mask, and method of fabricating biomolecule array or polymer array using the programmable mask and photochemical synthesis apparatus |
WO2007078833A2 (en) * | 2005-12-16 | 2007-07-12 | The Curators Of The University Of Missouri | Reusable pcr amplification system and method |
JP2007256001A (ja) * | 2006-03-22 | 2007-10-04 | Oki Electric Ind Co Ltd | 有機化合物合成装置および有機化合物合成用基板 |
JP2007252249A (ja) * | 2006-03-22 | 2007-10-04 | Oki Electric Ind Co Ltd | 有機化合物合成装置,光照射装置,有機化合物合成用基板および有機化合物の合成方法 |
EP1996947A1 (en) * | 2006-03-24 | 2008-12-03 | The Regents of the University of Michigan | Method for forming molecular sequences on surfaces |
US20070231805A1 (en) * | 2006-03-31 | 2007-10-04 | Baynes Brian M | Nucleic acid assembly optimization using clamped mismatch binding proteins |
KR100745990B1 (ko) * | 2006-07-17 | 2007-08-06 | 삼성전자주식회사 | 마이크로 어레이의 제조 방법 |
WO2008027558A2 (en) | 2006-08-31 | 2008-03-06 | Codon Devices, Inc. | Iterative nucleic acid assembly using activation of vector-encoded traits |
US9096953B2 (en) * | 2006-09-29 | 2015-08-04 | Intel Corporation | Method for high throughput, high volume manufacturing of biomolecule micro arrays |
US20080161204A1 (en) * | 2006-10-06 | 2008-07-03 | Mo-Huang Li | Microwell array for parallel synthesis of chain molecules |
US8345241B1 (en) | 2006-12-19 | 2013-01-01 | J. A. Woollam Co., Inc. | Application of digital light processor in imaging ellipsometer and the like systems |
WO2008082506A1 (en) * | 2006-12-19 | 2008-07-10 | J.A. Woollam Co., Inc. | Application of digital light processor in scanning spectrometer and imaging ellipsometer and the like systems |
US8749782B1 (en) | 2006-12-19 | 2014-06-10 | J.A. Woollam Co., Inc. | DLP base small spot investigation system |
JP2010516625A (ja) | 2007-01-24 | 2010-05-20 | インサート セラピューティクス, インコーポレイテッド | 制御された薬物送達のためのテザー基を有するポリマー−薬物コンジュゲート |
US20100093554A1 (en) * | 2007-06-01 | 2010-04-15 | Keting Chu | Methods for identifying biomarkers, autoantibody signatures, and stratifying subject groups using peptide arrays |
US8039612B2 (en) * | 2007-10-15 | 2011-10-18 | Honeywell International, Inc. | Synthesis of oligonucleotides or phosphorothioate oligonucleotide with a capping agent of N-methylimidazole free of 1,3,5-trimethylhexahydro-1,3,5-triazine |
US20100047876A1 (en) * | 2008-08-08 | 2010-02-25 | President And Fellows Of Harvard College | Hierarchical assembly of polynucleotides |
US8808986B2 (en) | 2008-08-27 | 2014-08-19 | Gen9, Inc. | Methods and devices for high fidelity polynucleotide synthesis |
US20100112558A1 (en) * | 2008-11-03 | 2010-05-06 | Xiaolian Gao | Probe Bead Synthesis and Use |
US10207240B2 (en) | 2009-11-03 | 2019-02-19 | Gen9, Inc. | Methods and microfluidic devices for the manipulation of droplets in high fidelity polynucleotide assembly |
EP2503888A4 (en) * | 2009-11-23 | 2015-07-29 | Cerulean Pharma Inc | POLYMERS ON CYCLODEXTRINBASIS FOR THERAPEUTIC ADMINISTRATION |
WO2011066185A1 (en) | 2009-11-25 | 2011-06-03 | Gen9, Inc. | Microfluidic devices and methods for gene synthesis |
WO2011066186A1 (en) | 2009-11-25 | 2011-06-03 | Gen9, Inc. | Methods and apparatuses for chip-based dna error reduction |
WO2011085075A2 (en) | 2010-01-07 | 2011-07-14 | Gen9, Inc. | Assembly of high fidelity polynucleotides |
US8716467B2 (en) | 2010-03-03 | 2014-05-06 | Gen9, Inc. | Methods and devices for nucleic acid synthesis |
US10240194B2 (en) | 2010-05-13 | 2019-03-26 | Gen9, Inc. | Methods for nucleotide sequencing and high fidelity polynucleotide synthesis |
WO2011150168A1 (en) | 2010-05-28 | 2011-12-01 | Gen9, Inc. | Methods and devices for in situ nucleic acid synthesis |
ES2548400T3 (es) | 2010-11-12 | 2015-10-16 | Gen9, Inc. | Métodos y dispositivos para la síntesis de ácidos nucleicos |
WO2012064975A1 (en) | 2010-11-12 | 2012-05-18 | Gen9, Inc. | Protein arrays and methods of using and making the same |
JP2012131718A (ja) | 2010-12-20 | 2012-07-12 | Samsung Electronics Co Ltd | 化合物合成方法、マイクロアレイ、酸転写用組成物及びバイオチップ製造用組成物 |
US8450131B2 (en) | 2011-01-11 | 2013-05-28 | Nanohmics, Inc. | Imprinted semiconductor multiplex detection array |
US9828696B2 (en) | 2011-03-23 | 2017-11-28 | Nanohmics, Inc. | Method for assembly of analyte filter arrays using biomolecules |
US9252175B2 (en) | 2011-03-23 | 2016-02-02 | Nanohmics, Inc. | Method for assembly of spectroscopic filter arrays using biomolecules |
US9752176B2 (en) | 2011-06-15 | 2017-09-05 | Ginkgo Bioworks, Inc. | Methods for preparative in vitro cloning |
WO2012174337A1 (en) | 2011-06-15 | 2012-12-20 | Gen9, Inc. | Methods for preparative in vitro cloning |
EP2944693B1 (en) | 2011-08-26 | 2019-04-24 | Gen9, Inc. | Compositions and methods for high fidelity assembly of nucleic acids |
JP2014531908A (ja) | 2011-10-14 | 2014-12-04 | プレジデント アンド フェローズ オブ ハーバード カレッジ | 構造アッセンブリによる配列決定 |
US9150853B2 (en) | 2012-03-21 | 2015-10-06 | Gen9, Inc. | Methods for screening proteins using DNA encoded chemical libraries as templates for enzyme catalysis |
EP4001427A1 (en) | 2012-04-24 | 2022-05-25 | Gen9, Inc. | Methods for sorting nucleic acids and multiplexed preparative in vitro cloning |
US9914967B2 (en) | 2012-06-05 | 2018-03-13 | President And Fellows Of Harvard College | Spatial sequencing of nucleic acids using DNA origami probes |
JP6509727B2 (ja) | 2012-06-25 | 2019-05-15 | ギンゴー バイオワークス, インコーポレイテッド | 核酸アセンブリおよび高処理シークエンシングのための方法 |
CN104662544B (zh) | 2012-07-19 | 2018-08-03 | 哈佛大学校长及研究员协会 | 利用核酸存储信息的方法 |
US20140094432A1 (en) | 2012-10-02 | 2014-04-03 | Cerulean Pharma Inc. | Methods and systems for polymer precipitation and generation of particles |
US9476089B2 (en) | 2012-10-18 | 2016-10-25 | President And Fellows Of Harvard College | Methods of making oligonucleotide probes |
US10138509B2 (en) | 2013-03-12 | 2018-11-27 | President And Fellows Of Harvard College | Method for generating a three-dimensional nucleic acid containing matrix |
TWI721929B (zh) | 2013-08-05 | 2021-03-11 | 美商扭轉生物科技有限公司 | 重新合成之基因庫 |
US9645391B2 (en) | 2013-11-27 | 2017-05-09 | Tokyo Electron Limited | Substrate tuning system and method using optical projection |
JP6676527B6 (ja) * | 2013-11-27 | 2020-05-20 | 東京エレクトロン株式会社 | 光学投影を使用する基板チューニングシステム及び方法 |
CA2961743A1 (en) * | 2014-09-17 | 2016-03-24 | Ibis Biosciences, Inc. | Sequencing by synthesis using pulse read optics |
CN107532129B (zh) | 2014-12-09 | 2022-09-13 | 生命技术公司 | 高效小体积核酸合成 |
CA2975852A1 (en) | 2015-02-04 | 2016-08-11 | Twist Bioscience Corporation | Methods and devices for de novo oligonucleic acid assembly |
WO2016126987A1 (en) | 2015-02-04 | 2016-08-11 | Twist Bioscience Corporation | Compositions and methods for synthetic gene assembly |
WO2016172377A1 (en) | 2015-04-21 | 2016-10-27 | Twist Bioscience Corporation | Devices and methods for oligonucleic acid library synthesis |
IL258164B (en) | 2015-09-18 | 2022-09-01 | Twist Bioscience Corp | Methods to regulate the activity of proteins and cells and a method for the production of nucleic acids |
WO2017053450A1 (en) | 2015-09-22 | 2017-03-30 | Twist Bioscience Corporation | Flexible substrates for nucleic acid synthesis |
CN108603307A (zh) | 2015-12-01 | 2018-09-28 | 特韦斯特生物科学公司 | 功能化表面及其制备 |
US10386351B2 (en) | 2015-12-07 | 2019-08-20 | Nanohmics, Inc. | Methods for detecting and quantifying analytes using gas species diffusion |
US10386365B2 (en) | 2015-12-07 | 2019-08-20 | Nanohmics, Inc. | Methods for detecting and quantifying analytes using ionic species diffusion |
KR102632268B1 (ko) * | 2016-01-11 | 2024-01-31 | 삼성전자주식회사 | 포토 레지스트 조성물 및 이를 이용한 반도체 장치의 제조 방법 |
WO2018038772A1 (en) | 2016-08-22 | 2018-03-01 | Twist Bioscience Corporation | De novo synthesized nucleic acid libraries |
JP6871364B2 (ja) | 2016-09-21 | 2021-05-12 | ツイスト バイオサイエンス コーポレーション | 核酸に基づくデータ保存 |
EA201991262A1 (ru) | 2016-12-16 | 2020-04-07 | Твист Байосайенс Корпорейшн | Библиотеки вариантов иммунологического синапса и их синтез |
SG11201907713WA (en) | 2017-02-22 | 2019-09-27 | Twist Bioscience Corp | Nucleic acid based data storage |
EP3595674A4 (en) | 2017-03-15 | 2020-12-16 | Twist Bioscience Corporation | BANKS OF VARIANTS OF IMMUNOLOGICAL SYNAPSE AND THEIR SYNTHESIS |
CN111566209A (zh) | 2017-06-12 | 2020-08-21 | 特韦斯特生物科学公司 | 无缝核酸装配方法 |
WO2018231864A1 (en) | 2017-06-12 | 2018-12-20 | Twist Bioscience Corporation | Methods for seamless nucleic acid assembly |
US20190009240A1 (en) * | 2017-07-10 | 2019-01-10 | The Charles Stark Draper Laboratory, Inc. | Apparatus Enabling High Density Information Storage in Molecular Chains |
US11407837B2 (en) | 2017-09-11 | 2022-08-09 | Twist Bioscience Corporation | GPCR binding proteins and synthesis thereof |
KR20240024357A (ko) | 2017-10-20 | 2024-02-23 | 트위스트 바이오사이언스 코포레이션 | 폴리뉴클레오타이드 합성을 위한 가열된 나노웰 |
US10936953B2 (en) | 2018-01-04 | 2021-03-02 | Twist Bioscience Corporation | DNA-based digital information storage with sidewall electrodes |
US20200384436A1 (en) * | 2018-01-05 | 2020-12-10 | Centrillion Technologies, Inc. | Methods for fabricating high resolution dna array and its application in sequencing |
KR20210013128A (ko) | 2018-05-18 | 2021-02-03 | 트위스트 바이오사이언스 코포레이션 | 핵산 하이브리드화를 위한 폴리뉴클레오타이드, 시약 및 방법 |
US11131615B2 (en) | 2018-06-07 | 2021-09-28 | Nanohmics, Inc. | Sensor and methods for detecting and quantifying ions and molecules |
JP7430701B2 (ja) | 2018-07-23 | 2024-02-13 | ディーエヌエー スクリプト | 核酸鎖の大規模並列酵素合成 |
SG11202109283UA (en) | 2019-02-26 | 2021-09-29 | Twist Bioscience Corp | Variant nucleic acid libraries for antibody optimization |
AU2020229349A1 (en) | 2019-02-26 | 2021-10-14 | Twist Bioscience Corporation | Variant nucleic acid libraries for GLP1 receptor |
EP3987019A4 (en) | 2019-06-21 | 2023-04-19 | Twist Bioscience Corporation | BARCODE-BASED NUCLEIC ACID SEQUENCE ARRANGEMENT |
CN114729389B (zh) | 2019-09-23 | 2024-03-08 | Dna斯克瑞普特公司 | 增加多核苷酸的无模板酶促合成中的长序列产率 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5143854A (en) * | 1989-06-07 | 1992-09-01 | Affymax Technologies N.V. | Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof |
WO1993002992A1 (en) * | 1991-08-07 | 1993-02-18 | H & N Instruments, Inc. | Synthesis of chain chemical compounds |
WO1996011878A1 (en) * | 1994-10-18 | 1996-04-25 | The Regents Of The University Of California | The combinatorial synthesis of novel materials |
US5677195A (en) * | 1991-11-22 | 1997-10-14 | Affymax Technologies N.V. | Combinatorial strategies for polymer synthesis |
WO1997039151A1 (en) * | 1996-04-17 | 1997-10-23 | Affymetrix, Inc. | Photolabile polymer array synthesis methods |
Family Cites Families (84)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2644341C2 (de) * | 1976-10-01 | 1984-08-02 | Ernst Leitz Wetzlar Gmbh, 6330 Wetzlar | Verfahren und Anordnungen zur automatischen Verwirklichung des Köhler'schen Beleuchtungsprinzipes |
US4146329A (en) * | 1977-09-14 | 1979-03-27 | The United States Of America As Represented By The Secretary Of The Navy | Autoalignment system for high power laser |
JPS5534490A (en) * | 1978-09-01 | 1980-03-11 | Canon Inc | Alignment device |
US4367251A (en) * | 1980-04-21 | 1983-01-04 | General Electric Company | UV Curable compositions and substrates treated therewith |
US4571603A (en) * | 1981-11-03 | 1986-02-18 | Texas Instruments Incorporated | Deformable mirror electrostatic printer |
US4719615A (en) * | 1983-08-22 | 1988-01-12 | Optical Data, Inc. | Erasable optical data storage medium |
US4662746A (en) * | 1985-10-30 | 1987-05-05 | Texas Instruments Incorporated | Spatial light modulator and method |
US4596992A (en) * | 1984-08-31 | 1986-06-24 | Texas Instruments Incorporated | Linear spatial light modulator and printer |
US5096279A (en) * | 1984-08-31 | 1992-03-17 | Texas Instruments Incorporated | Spatial light modulator and method |
US4615595A (en) * | 1984-10-10 | 1986-10-07 | Texas Instruments Incorporated | Frame addressed spatial light modulator |
US5202231A (en) * | 1987-04-01 | 1993-04-13 | Drmanac Radoje T | Method of sequencing of genomes by hybridization of oligonucleotide probes |
US5525464A (en) * | 1987-04-01 | 1996-06-11 | Hyseq, Inc. | Method of sequencing by hybridization of oligonucleotide probes |
US6031091A (en) | 1987-09-21 | 2000-02-29 | Gen-Probe Incorporated | Non-nucleotide linking reagents for nucleotide probes |
US5585481A (en) * | 1987-09-21 | 1996-12-17 | Gen-Probe Incorporated | Linking reagents for nucleotide probes |
US5158855A (en) | 1987-09-24 | 1992-10-27 | Hitachi, Ltd. | α-diazoacetoacetates and photosensitive resin compositions containing the same |
US5028939A (en) * | 1988-08-23 | 1991-07-02 | Texas Instruments Incorporated | Spatial light modulator system |
US5744101A (en) * | 1989-06-07 | 1998-04-28 | Affymax Technologies N.V. | Photolabile nucleoside protecting groups |
US5424186A (en) | 1989-06-07 | 1995-06-13 | Affymax Technologies N.V. | Very large scale immobilized polymer synthesis |
US5141813A (en) * | 1989-08-28 | 1992-08-25 | Clontech Laboratories, Inc. | Multifunctional controlled pore glass reagent for solid phase oligonucleotide synthesis |
US5252743A (en) * | 1989-11-13 | 1993-10-12 | Affymax Technologies N.V. | Spatially-addressable immobilization of anti-ligands on surfaces |
US5083857A (en) * | 1990-06-29 | 1992-01-28 | Texas Instruments Incorporated | Multi-level deformable mirror device |
DE69132531T2 (de) * | 1990-12-06 | 2001-09-13 | Affymetrix Inc | Verbindungen und ihre Verwendung in einer binären Synthesestrategie |
US5401607A (en) * | 1991-04-17 | 1995-03-28 | Polaroid Corporation | Processes and compositions for photogeneration of acid |
US5474796A (en) | 1991-09-04 | 1995-12-12 | Protogene Laboratories, Inc. | Method and apparatus for conducting an array of chemical reactions on a support surface |
EP0537524A1 (en) | 1991-10-17 | 1993-04-21 | Shipley Company Inc. | Radiation sensitive compositions and methods |
US5846708A (en) | 1991-11-19 | 1998-12-08 | Massachusetts Institiute Of Technology | Optical and electrical methods and apparatus for molecule detection |
US5384261A (en) * | 1991-11-22 | 1995-01-24 | Affymax Technologies N.V. | Very large scale immobilized polymer synthesis using mechanically directed flow paths |
US5412087A (en) * | 1992-04-24 | 1995-05-02 | Affymax Technologies N.V. | Spatially-addressable immobilization of oligonucleotides and other biological polymers on surfaces |
US5247180A (en) * | 1991-12-30 | 1993-09-21 | Texas Instruments Incorporated | Stereolithographic apparatus and method of use |
US5656741A (en) * | 1992-03-30 | 1997-08-12 | Barrskogen, Inc. | Process and reagents for processing synthetic oligonucleotides |
GB9207381D0 (en) * | 1992-04-03 | 1992-05-13 | Ici Plc | Synthesis of oligonucleotides |
US6219015B1 (en) | 1992-04-28 | 2001-04-17 | The Board Of Directors Of The Leland Stanford, Junior University | Method and apparatus for using an array of grating light valves to produce multicolor optical images |
US5324483B1 (en) * | 1992-10-08 | 1996-09-24 | Warner Lambert Co | Apparatus for multiple simultaneous synthesis |
US5837832A (en) * | 1993-06-25 | 1998-11-17 | Affymetrix, Inc. | Arrays of nucleic acid probes on biological chips |
DE4331012A1 (de) * | 1993-09-13 | 1995-03-16 | Bayer Ag | Nukleinsäuren-bindende Oligomere mit N-Verzweigung für Therapie und Diagnostik |
US5583688A (en) * | 1993-12-21 | 1996-12-10 | Texas Instruments Incorporated | Multi-level digital micromirror device |
US5578832A (en) * | 1994-09-02 | 1996-11-26 | Affymetrix, Inc. | Method and apparatus for imaging a sample on a device |
US5631734A (en) * | 1994-02-10 | 1997-05-20 | Affymetrix, Inc. | Method and apparatus for detection of fluorescently labeled materials |
US6051374A (en) | 1994-02-14 | 2000-04-18 | Abbott Laboratories | Non-A, non-B, non-C, non-D, non-E hepatitis reagents and methods for their use |
US5517280A (en) * | 1994-04-12 | 1996-05-14 | The Board Of Trustees Of The Leland Stanford, Jr. University | Photolithography system |
US5666190A (en) * | 1994-04-12 | 1997-09-09 | The Board Of Trustees Of The Leland Stanford, Jr. University | Method of performing lithography using cantilever array |
US5883705A (en) * | 1994-04-12 | 1999-03-16 | The Board Of Trustees Of The Leland Stanford, Jr. University | Atomic force microscope for high speed imaging including integral actuator and sensor |
US5514789A (en) | 1994-04-21 | 1996-05-07 | Barrskogen, Inc. | Recovery of oligonucleotides by gas phase cleavage |
US5571639A (en) * | 1994-05-24 | 1996-11-05 | Affymax Technologies N.V. | Computer-aided engineering system for design of sequence arrays and lithographic masks |
US5539567A (en) * | 1994-06-16 | 1996-07-23 | Texas Instruments Incorporated | Photolithographic technique and illuminator using real-time addressable phase shift light shift |
AU689924B2 (en) * | 1994-06-23 | 1998-04-09 | Affymax Technologies N.V. | Photolabile compounds and methods for their use |
US5552471A (en) * | 1994-08-17 | 1996-09-03 | The Perkin-Elmer Corporation | Solid support reagents for the synthesis of 3'-Nitrogen containing polynucleotides |
US5556752A (en) * | 1994-10-24 | 1996-09-17 | Affymetrix, Inc. | Surface-bound, unimolecular, double-stranded DNA |
US5504614A (en) * | 1995-01-31 | 1996-04-02 | Texas Instruments Incorporated | Method for fabricating a DMD spatial light modulator with a hardened hinge |
US5599695A (en) * | 1995-02-27 | 1997-02-04 | Affymetrix, Inc. | Printing molecular library arrays using deprotection agents solely in the vapor phase |
US5535047A (en) * | 1995-04-18 | 1996-07-09 | Texas Instruments Incorporated | Active yoke hidden hinge digital micromirror device |
US5624711A (en) | 1995-04-27 | 1997-04-29 | Affymax Technologies, N.V. | Derivatization of solid supports and methods for oligomer synthesis |
TW284907B (en) * | 1995-06-07 | 1996-09-01 | Cauldron Lp | Removal of material by polarized irradiation and back side application for radiation |
US5835256A (en) * | 1995-06-19 | 1998-11-10 | Reflectivity, Inc. | Reflective spatial light modulator with encapsulated micro-mechanical elements |
JP2000502341A (ja) | 1995-12-22 | 2000-02-29 | ユーニヴァスィティ テクノロヂィズ インタナショナル インク. | オリゴヌクレオチド合成のための再利用可能の固体支持体、その製法、およびその使用法 |
US6043353A (en) | 1995-12-22 | 2000-03-28 | University Technologies International, Inc. | Reusable solid support for oligonucleotide synthesis, process for production thereof and process for use thereof |
US5567294A (en) * | 1996-01-30 | 1996-10-22 | Board Of Governors, University Of Alberta | Multiple capillary biochemical analyzer with barrier member |
US5869696A (en) | 1996-04-22 | 1999-02-09 | Beckman Instruments, Inc. | Universal solid supports and methods for their use |
US6005125A (en) | 1996-05-06 | 1999-12-21 | Rutgers The State University Of New Jersey | Universal allyl linker for solid-phase nucleic acid synthesis |
JP3456348B2 (ja) * | 1996-09-19 | 2003-10-14 | トヨタ自動車株式会社 | ディーゼル機関の排気浄化装置 |
US5942608A (en) | 1996-10-29 | 1999-08-24 | Council of Sciemtific & Industrial Research and Department of Biotechnology | Process for preparing a universal support for the synthesis of oligonucleotides |
US5953153A (en) * | 1996-10-29 | 1999-09-14 | Texas Instruments Incorporated | Spatial light modulator with improved light shield |
WO1998020967A1 (en) | 1996-11-14 | 1998-05-22 | Affymetrix, Inc. | Chemical amplification for the synthesis of patterned arrays |
US5750672A (en) | 1996-11-22 | 1998-05-12 | Barrskogen, Inc. | Anhydrous amine cleavage of oligonucleotides |
DE19707432A1 (de) * | 1997-02-25 | 1998-08-27 | Bodenseewerk Geraetetech | Vorrichtung zur Umschaltung von optischen Bildern zwischen verschiedenen Kanälen |
US5768009A (en) * | 1997-04-18 | 1998-06-16 | E-Beam | Light valve target comprising electrostatically-repelled micro-mirrors |
US6210878B1 (en) * | 1997-08-08 | 2001-04-03 | The Regents Of The University Of California | Array-based detection of genetic alterations associated with disease |
AU9220498A (en) | 1997-09-04 | 1999-03-22 | Bayer Corporation | Oligonucleotide probes bearing quenchable fluorescent labels, and methods of usethereof |
US20040035690A1 (en) * | 1998-02-11 | 2004-02-26 | The Regents Of The University Of Michigan | Method and apparatus for chemical and biochemical reactions using photo-generated reagents |
CA2319587C (en) | 1998-02-11 | 2004-09-21 | University Of Houston | Method and apparatus for chemical and biochemical reactions using photo-generated reagents |
EP2259046A3 (en) * | 1998-02-23 | 2011-11-30 | Wisconsin Alumni Research Foundation | Method for synthesis of arrays of dna probes |
US6271957B1 (en) * | 1998-05-29 | 2001-08-07 | Affymetrix, Inc. | Methods involving direct write optical lithography |
US6295153B1 (en) * | 1998-06-04 | 2001-09-25 | Board Of Regents, The University Of Texas System | Digital optical chemistry micromirror imager |
US6215579B1 (en) * | 1998-06-24 | 2001-04-10 | Silicon Light Machines | Method and apparatus for modulating an incident light beam for forming a two-dimensional image |
WO2000012524A1 (en) | 1998-08-27 | 2000-03-09 | Bayer Corporation | Purification of oligomers using dual-end selection |
DE59915204D1 (de) | 1998-08-28 | 2010-10-28 | Febit Holding Gmbh | Verfahren zur herstellung von biochemischen reaktionsträgern |
US5991066A (en) * | 1998-10-15 | 1999-11-23 | Memsolutions, Inc. | Membrane-actuated charge controlled mirror |
EP1149109B1 (en) | 1999-02-05 | 2009-09-16 | Amersham Biosciences Corp. | Method for deprotecting oligonucleotides |
WO2000047598A1 (en) | 1999-02-10 | 2000-08-17 | Macrogen Inc. | Method and apparatus for compound library preparation using optical modulator |
JP2002538790A (ja) | 1999-03-08 | 2002-11-19 | プロトジーン・ラボラトリーズ・インコーポレーテッド | 長いdna配列を経済的に合成し、そして組み立てるための方法および組成物 |
DE19914279C1 (de) * | 1999-03-25 | 2000-09-07 | Jena Optronik Gmbh | Anordnung zum optischen Auslesen der Information von einem matrixförmigen Substrat mit einer Vielzahl von Einzelproben |
AU2001272714A1 (en) | 2000-06-13 | 2001-12-24 | Proligo Llc | Universal solid supports for solid phase oligosynthesis and methods for their preparation and use |
US6869696B2 (en) * | 2002-05-10 | 2005-03-22 | Sensient Imaging Technologies Gmbh | Organic red electro-luminescent device including a heterocyclic emitter |
JP4505763B2 (ja) | 2007-01-31 | 2010-07-21 | ヒューレット−パッカード デベロップメント カンパニー エル.ピー. | ノードクラスタの管理 |
-
1999
- 1999-02-10 CA CA002319587A patent/CA2319587C/en not_active Expired - Fee Related
- 1999-02-10 WO PCT/US1999/002945 patent/WO1999041007A2/en active IP Right Grant
- 1999-02-10 JP JP2000531248A patent/JP4503828B2/ja not_active Expired - Fee Related
- 1999-02-10 EP EP10180861A patent/EP2332645A1/en not_active Withdrawn
- 1999-02-10 AU AU26714/99A patent/AU755239B2/en not_active Ceased
- 1999-02-10 AT AT99906913T patent/ATE246041T1/de not_active IP Right Cessation
- 1999-02-10 US US09/248,093 patent/US6426184B1/en not_active Expired - Lifetime
- 1999-02-10 EP EP99906913A patent/EP1054726B1/en not_active Revoked
- 1999-02-10 DE DE69909972T patent/DE69909972T2/de not_active Revoked
-
2002
- 2002-05-29 US US10/157,442 patent/US7838466B2/en not_active Expired - Fee Related
- 2002-09-11 US US10/241,411 patent/US7491680B2/en not_active Expired - Fee Related
- 2002-12-04 US US10/309,627 patent/US20030186427A1/en not_active Abandoned
-
2003
- 2003-01-13 US US10/340,928 patent/US7544638B2/en not_active Expired - Lifetime
- 2003-04-21 US US10/419,380 patent/US20040023368A1/en not_active Abandoned
-
2010
- 2010-11-19 US US12/949,988 patent/US20110170075A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5143854A (en) * | 1989-06-07 | 1992-09-01 | Affymax Technologies N.V. | Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof |
WO1993002992A1 (en) * | 1991-08-07 | 1993-02-18 | H & N Instruments, Inc. | Synthesis of chain chemical compounds |
US5677195A (en) * | 1991-11-22 | 1997-10-14 | Affymax Technologies N.V. | Combinatorial strategies for polymer synthesis |
WO1996011878A1 (en) * | 1994-10-18 | 1996-04-25 | The Regents Of The University Of California | The combinatorial synthesis of novel materials |
WO1997039151A1 (en) * | 1996-04-17 | 1997-10-23 | Affymetrix, Inc. | Photolabile polymer array synthesis methods |
Non-Patent Citations (1)
Title |
---|
See also references of EP1054726A2 * |
Cited By (86)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7491680B2 (en) | 1998-02-11 | 2009-02-17 | The Regents Of The University Of Michigan | Device for chemical and biochemical reactions using photo-generated reagents |
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US6375903B1 (en) | 1998-02-23 | 2002-04-23 | Wisconsin Alumni Research Foundation | Method and apparatus for synthesis of arrays of DNA probes |
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US6271957B1 (en) | 1998-05-29 | 2001-08-07 | Affymetrix, Inc. | Methods involving direct write optical lithography |
EP0961174A2 (en) * | 1998-05-29 | 1999-12-01 | Affymetrix, Inc. (a California Corporation) | Compositions and methods involving direct write optical lithography |
US6480324B2 (en) | 1998-05-29 | 2002-11-12 | Affymetrix, Inc. | Methods involving direct write optical lithography |
US6295153B1 (en) | 1998-06-04 | 2001-09-25 | Board Of Regents, The University Of Texas System | Digital optical chemistry micromirror imager |
US8415101B2 (en) | 1998-06-04 | 2013-04-09 | Roche Nimblegen, Inc. | Digital optical chemistry micromirror imager |
EP2273270A1 (de) * | 1998-08-28 | 2011-01-12 | febit holding GmbH | Verfahren und Vorrichtung zur Herstellung und/oder Analyse von biochemischen Reaktionsträgern |
WO2000013017A3 (de) * | 1998-08-28 | 2000-07-20 | Febit Ferrarius Biotech Gmbh | Verfahren und vorrichtung zur herstellung und/oder analyse von biochemischen reaktionsträgern |
WO2000013017A2 (de) * | 1998-08-28 | 2000-03-09 | Febit Ferrarius Biotechnology Gmbh | Verfahren und vorrichtung zur herstellung und/oder analyse von biochemischen reaktionsträgern |
US7097974B1 (en) | 1998-08-28 | 2006-08-29 | Febit Biotech Gmbh | Support for a method for determining an analyte and a method for producing the support |
EP1180111A1 (en) * | 1999-02-10 | 2002-02-20 | Macrogen Inc. | Method and apparatus for compound library preparation using optical modulator |
EP1180111A4 (en) * | 1999-02-10 | 2003-03-26 | Macrogen Inc | METHOD AND DEVICE FOR PRODUCING CONNECTION LIBRARIES BY MEANS OF OPTICAL MODULATOR |
FR2798675A1 (fr) * | 1999-09-16 | 2001-03-23 | Centre Nat Rech Scient | Procede et dispositif de fabrication d'un support porteur d'une pluralite de sequences polynucleotidiques et/ou peptidiques differentes |
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JP2004501665A (ja) * | 2000-07-03 | 2004-01-22 | ゼオトロン コーポレイション | 光生成試薬を用いて化学反応を行なうためのデバイスおよび方法 |
WO2002026373A1 (fr) * | 2000-09-27 | 2002-04-04 | Centre National De La Recherche Scientifique (C.N.R.S.) | Procede et dispositif de fabrication d'un support porteur d'une pluralite de sequences polynucleotidiques et/ou peptidiques differentes |
US7470540B2 (en) | 2000-10-17 | 2008-12-30 | Febit Ag | Method and device for the integrated synthesis and analysis of analytes on a support |
US7435575B2 (en) | 2000-12-28 | 2008-10-14 | Roche Molecular Systems, Inc. | Method for processing a nucleic acid sample by oscillating a cartridge, a system and a cartridge for performing such a method |
US7807807B2 (en) | 2001-03-14 | 2010-10-05 | The Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
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US7211654B2 (en) | 2001-03-14 | 2007-05-01 | Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
US8053187B2 (en) | 2001-03-14 | 2011-11-08 | The Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
US8461317B2 (en) | 2001-03-14 | 2013-06-11 | The Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
US9303055B2 (en) | 2001-03-14 | 2016-04-05 | The Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
US7553958B2 (en) | 2001-03-14 | 2009-06-30 | The Regents Of The University Of Michigan | Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports |
US6855501B2 (en) | 2001-03-26 | 2005-02-15 | Linden Technologies, Inc. | Transfer of arrayed chemical compositions |
US6838447B2 (en) | 2001-03-26 | 2005-01-04 | Linden Technologies, Inc. | Particulate compositions for chemical synthesis |
WO2003000644A1 (en) * | 2001-06-21 | 2003-01-03 | The Institute Of Cancer Research | Photolabile esters and their uses |
US7301049B2 (en) | 2001-06-21 | 2007-11-27 | The Institute Of Cancer Research | Photolabile esters and their uses |
WO2003008088A3 (de) * | 2001-07-17 | 2003-05-30 | Frieder Breitling | Verfahren und anordnung zum anbringen von in transportmitteln immobilisierten substanzen sowie monomerpartikel |
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WO2004004885A1 (de) * | 2002-07-05 | 2004-01-15 | Marcel Rogalla | Verfahren und programmierbare beleuchtungsvorrichtung zur hochauflösenden, massiv parallelen, räumlichen synthese und analyse von microarrays |
US7354777B2 (en) | 2002-08-07 | 2008-04-08 | International Business Machines Corporation | Discrete nano-textured structures in biomolecular arrays, and method of use |
US6962822B2 (en) | 2002-08-07 | 2005-11-08 | International Business Machines Corporation | Discrete nano-textured structures in biomolecular arrays, and method of use |
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US10640764B2 (en) | 2002-09-12 | 2020-05-05 | Gen9, Inc. | Microarray synthesis and assembly of gene-length polynucleotides |
US10774325B2 (en) | 2002-09-12 | 2020-09-15 | Gen9, Inc. | Microarray synthesis and assembly of gene-length polynucleotides |
EP1547678A3 (en) * | 2003-12-22 | 2005-09-21 | Affymetrix, Inc. (a Delaware Corporation) | Process for high-yield synthesis of nucleic acid arrays |
WO2006117556A2 (en) * | 2005-05-04 | 2006-11-09 | The Institute Of Cancer Research: Royal Cancer Hospital | Materials and methods for the photodirected synthesis of oligonucleotide arrays |
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US7722824B2 (en) | 2005-08-02 | 2010-05-25 | Wisconsin Alumni Research Foundation | Synthesis of arrays of oligonucleotides and other chain molecules |
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US8062844B2 (en) | 2005-12-29 | 2011-11-22 | Affymetrix, Inc. | Use of acid scavengers for the synthesis of standard length and long-mer nucleic acid arrays |
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US8822158B2 (en) | 2009-02-25 | 2014-09-02 | Roche Molecular Systems, Inc. | Miniaturized, high-throughput nucleic acid analysis |
US9347092B2 (en) | 2009-02-25 | 2016-05-24 | Roche Molecular System, Inc. | Solid support for high-throughput nucleic acid analysis |
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Also Published As
Publication number | Publication date |
---|---|
AU2671499A (en) | 1999-08-30 |
EP1054726B1 (en) | 2003-07-30 |
CA2319587A1 (en) | 1999-08-19 |
US20040023368A1 (en) | 2004-02-05 |
US20030143131A1 (en) | 2003-07-31 |
CA2319587C (en) | 2004-09-21 |
DE69909972T2 (de) | 2004-05-13 |
US20080318806A1 (en) | 2008-12-25 |
WO1999041007B1 (en) | 2000-01-13 |
AU755239B2 (en) | 2002-12-05 |
US20020081582A1 (en) | 2002-06-27 |
US7491680B2 (en) | 2009-02-17 |
US20110170075A1 (en) | 2011-07-14 |
JP2002502698A (ja) | 2002-01-29 |
JP4503828B2 (ja) | 2010-07-14 |
US20030138363A1 (en) | 2003-07-24 |
WO1999041007A3 (en) | 1999-11-11 |
US7544638B2 (en) | 2009-06-09 |
ATE246041T1 (de) | 2003-08-15 |
EP1054726A2 (en) | 2000-11-29 |
US20030186427A1 (en) | 2003-10-02 |
US6426184B1 (en) | 2002-07-30 |
US7838466B2 (en) | 2010-11-23 |
DE69909972D1 (de) | 2003-09-04 |
EP2332645A1 (en) | 2011-06-15 |
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