BRPI0518207B1 - Método de separação de um ou mais anticorpos de um ou mais outros compostos em uma amostra líquida - Google Patents
Método de separação de um ou mais anticorpos de um ou mais outros compostos em uma amostra líquida Download PDFInfo
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- BRPI0518207B1 BRPI0518207B1 BRPI0518207-7A BRPI0518207A BRPI0518207B1 BR PI0518207 B1 BRPI0518207 B1 BR PI0518207B1 BR PI0518207 A BRPI0518207 A BR PI0518207A BR PI0518207 B1 BRPI0518207 B1 BR PI0518207B1
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- Treatment Of Liquids With Adsorbents In General (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (5)
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| SE0402558A SE0402558D0 (sv) | 2004-10-21 | 2004-10-21 | A process for the purification of antibodies |
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| SE0402910 | 2004-11-26 | ||
| PCT/SE2005/001591 WO2006043895A1 (en) | 2004-10-21 | 2005-10-21 | A method of antibody purification |
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| WO2005073711A2 (en) | 2004-01-20 | 2005-08-11 | Pall Corporation | Chromatographic material for the absorption of proteins at physiological ionic strength |
| JP4831436B2 (ja) | 2004-10-21 | 2011-12-07 | ジーイー・ヘルスケア・バイオサイエンス・アクチボラグ | クロマトグラフィーリガンド |
| US9910341B2 (en) | 2005-01-31 | 2018-03-06 | The Invention Science Fund I, Llc | Shared image device designation |
| US9489717B2 (en) | 2005-01-31 | 2016-11-08 | Invention Science Fund I, Llc | Shared image device |
| US8606383B2 (en) | 2005-01-31 | 2013-12-10 | The Invention Science Fund I, Llc | Audio sharing |
| US8902320B2 (en) | 2005-01-31 | 2014-12-02 | The Invention Science Fund I, Llc | Shared image device synchronization or designation |
| US20060170956A1 (en) | 2005-01-31 | 2006-08-03 | Jung Edward K | Shared image devices |
| US9325781B2 (en) | 2005-01-31 | 2016-04-26 | Invention Science Fund I, Llc | Audio sharing |
| US9082456B2 (en) | 2005-01-31 | 2015-07-14 | The Invention Science Fund I Llc | Shared image device designation |
| US20060174203A1 (en) | 2005-01-31 | 2006-08-03 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Viewfinder for shared image device |
| US9124729B2 (en) | 2005-01-31 | 2015-09-01 | The Invention Science Fund I, Llc | Shared image device synchronization or designation |
| TW200639190A (en) * | 2005-02-04 | 2006-11-16 | Showa Denko Kk | Packing material for ion chromatography |
| US9967424B2 (en) | 2005-06-02 | 2018-05-08 | Invention Science Fund I, Llc | Data storage usage protocol |
| US9001215B2 (en) | 2005-06-02 | 2015-04-07 | The Invention Science Fund I, Llc | Estimating shared image device operational capabilities or resources |
| US9942511B2 (en) | 2005-10-31 | 2018-04-10 | Invention Science Fund I, Llc | Preservation/degradation of video/audio aspects of a data stream |
| US8681225B2 (en) | 2005-06-02 | 2014-03-25 | Royce A. Levien | Storage access technique for captured data |
| US9819490B2 (en) | 2005-05-04 | 2017-11-14 | Invention Science Fund I, Llc | Regional proximity for shared image device(s) |
| US10003762B2 (en) | 2005-04-26 | 2018-06-19 | Invention Science Fund I, Llc | Shared image devices |
| US9451200B2 (en) | 2005-06-02 | 2016-09-20 | Invention Science Fund I, Llc | Storage access technique for captured data |
| US9093121B2 (en) | 2006-02-28 | 2015-07-28 | The Invention Science Fund I, Llc | Data management of an audio data stream |
| NZ611859A (en) | 2006-04-05 | 2014-12-24 | Abbvie Biotechnology Ltd | Antibody purification |
| US9375499B2 (en) | 2006-07-14 | 2016-06-28 | Wisconsin Alumni Research Foundation | Adsorptive membranes for trapping viruses |
| US7999085B2 (en) * | 2007-01-09 | 2011-08-16 | Bio-Rad Laboratories, Inc. | Enhanced capacity and purification of protein by mixed mode chromatography in the presence of aqueous-soluble nonionic organic polymers |
| US7691980B2 (en) * | 2007-01-09 | 2010-04-06 | Bio-Rad Laboratories, Inc. | Enhanced capacity and purification of antibodies by mixed mode chromatography in the presence of aqueous-soluble nonionic organic polymers |
| US8092683B2 (en) * | 2007-01-10 | 2012-01-10 | Ge Healthcare Bio-Sciences Ab | Multi-modal ion exchange chromatography resins |
| AU2008279841B2 (en) | 2007-07-25 | 2013-05-02 | Cytiva Bioprocess R&D Ab | Separation matrix |
| KR101163307B1 (ko) * | 2007-10-26 | 2012-07-05 | 아사히 가세이 케미칼즈 가부시키가이샤 | 단백질의 정제 방법 |
| WO2009058769A1 (en) * | 2007-10-30 | 2009-05-07 | Schering Corporation | Purification of antibodies containing hydrophobic variants |
| EP2265129B1 (en) * | 2008-04-08 | 2015-10-28 | Bio-Rad Laboratories, Inc. | Chromatography purification of antibodies |
| DE102008018734B4 (de) * | 2008-04-14 | 2013-03-21 | Sartorius Stedim Biotech Gmbh | Hydrophobe Cellulose-Membran, Verfahren zu ihrer Herstellung und ihre Verwendung in der hydrophoben Interaktionschromatographie |
| DE102008018732B4 (de) * | 2008-04-14 | 2022-06-09 | Sartorius Stedim Biotech Gmbh | Verfahren zur Stofftrennung unter Verwendung einer Cellulosehydrat-Membran in der Größenausschlusschromatographie |
| DE102008055821A1 (de) * | 2008-04-14 | 2009-10-15 | Sartorius Stedim Biotech Gmbh | Cellulosehydrat-Membran, Verfahren zur ihrer Herstellung und Verwendung davon |
| FR2931838B1 (fr) | 2008-06-02 | 2010-06-11 | Millipore Corp | Installation pour traiter un liquide biologique. |
| WO2010030222A1 (en) * | 2008-09-12 | 2010-03-18 | Ge Healthcare Bio-Sciences Ab | Enhanced protein aggregate removal with multimodal anion exchangers in the presence of protein-excluded zwitterions |
| WO2010071208A1 (ja) * | 2008-12-19 | 2010-06-24 | 武田薬品工業株式会社 | 抗体の精製方法 |
| FR2940145B1 (fr) | 2008-12-24 | 2011-03-25 | Millipore Corp | Chariot et installation de traitement d'un liquide biologique |
| JP2010158624A (ja) * | 2009-01-08 | 2010-07-22 | Asahi Kasei Chemicals Corp | 多孔質吸着膜、及び当該多孔質吸着膜を用いたたんぱく質の精製方法 |
| FR2941385B1 (fr) | 2009-01-23 | 2011-04-01 | Millipore Corp | Procede pour fournir un circuit pour liquide biologique et circuit obtenu. |
| US9441011B2 (en) | 2009-07-03 | 2016-09-13 | Asahi Kasei Chemicals Corporation | Method for purification of antibody using porous membrane having amino group and alkyl group both bound to graft chain immobilized on porous substrate |
| EP2459308A1 (en) | 2009-07-28 | 2012-06-06 | instrAction GmbH | Specific sorbent for binding proteins and peptides, and separation method using the same |
| US8277649B2 (en) | 2009-12-14 | 2012-10-02 | General Electric Company | Membranes and associated methods for purification of antibodies |
| FR2955119B1 (fr) | 2010-01-13 | 2012-12-28 | Millipore Corp | Circuit pour liquide biologique |
| EP4492053A3 (en) | 2010-05-25 | 2025-03-19 | F. Hoffmann-La Roche AG | Methods of purifying polypeptides |
| FR2960796B1 (fr) | 2010-06-08 | 2014-01-24 | Millipore Corp | Dispositif pour une installation de traitement de liquide biologique |
| FR2960795B1 (fr) | 2010-06-08 | 2012-07-27 | Millipore Corp | Dispositif pour une installation de traitement de liquide biologique |
| FR2960794B1 (fr) | 2010-06-08 | 2012-07-27 | Millipore Corp | Dispositif pour une installation de traitement de liquide biologique |
| FR2961713B1 (fr) | 2010-06-23 | 2012-08-10 | Millipore Corp | Poche pour circuit d'une installation de traitement de liquide biologique |
| FR2961711B1 (fr) | 2010-06-23 | 2012-08-17 | Millipore Corp | Poche pour circuit d'une installation de traitement de liquide biologique |
| KR101997543B1 (ko) | 2010-07-30 | 2019-07-09 | 이엠디 밀리포어 코포레이션 | 크로마토그래피 매질 및 방법 |
| FR2963573B1 (fr) | 2010-08-03 | 2012-08-31 | Millipore Corp | Chariot de pompage pour une installation de traitement de liquide biologique |
| MX2013003182A (es) * | 2010-09-20 | 2013-04-24 | Abbvie Inc | Purificacion de anticuerpos por cromatografia de lecho movil simulada. |
| EP2655412B1 (en) * | 2010-12-21 | 2018-01-17 | F. Hoffmann-La Roche AG | Isoform enriched antibody preparation and method for obtaining it |
| FR2973396B1 (fr) | 2011-03-28 | 2013-05-10 | Millipore Corp | Installation de traitement de liquide biologique |
| EP2702077A2 (en) | 2011-04-27 | 2014-03-05 | AbbVie Inc. | Methods for controlling the galactosylation profile of recombinantly-expressed proteins |
| EP2570184A1 (en) * | 2011-09-15 | 2013-03-20 | InstrAction GmbH | Sorbent comprising on its surface an aromatic ring system having an anionic or deprotonizable group for the purification of organic molecules |
| EP2570185A1 (en) * | 2011-09-15 | 2013-03-20 | InstrAction GmbH | Sorbent comprising an aromatic ring system on its surface for the purification of organic molecules |
| US8802448B2 (en) | 2011-07-27 | 2014-08-12 | Pall Corporation | Mixed mode ligands |
| EP2578286A1 (en) * | 2011-10-04 | 2013-04-10 | Merck Patent GmbH | Method and apparatus for chromatographic purification |
| DK2768857T3 (da) * | 2011-10-19 | 2020-02-03 | Novimmune Sa | Fremgangsmåder til oprensning af antistoffer |
| US9309282B2 (en) | 2011-10-19 | 2016-04-12 | Bio-Rad Laboratories, Inc. | Solid phase for mixed-mode chromatographic purification of proteins |
| EP2773439A4 (en) * | 2011-10-31 | 2015-07-01 | Merck Sharp & Dohme | CHROMATOGRAPHY METHOD FOR RESOLVING HETEROGENIC ANTIBODY AGGREGATES |
| WO2013075740A1 (en) * | 2011-11-23 | 2013-05-30 | Sanofi | Antibody purification method |
| EP2782925B1 (en) * | 2011-11-23 | 2024-03-06 | Sanofi | Protein purification using bis-tris buffer |
| CN104812491B (zh) | 2012-03-08 | 2018-06-19 | 生物辐射实验室股份有限公司 | 阴离子交换-疏水性混合模式 |
| SG10201701224UA (en) * | 2012-03-12 | 2017-04-27 | Merck Patent Gmbh | Removal of protein aggregates from biopharmaceutical preparations in a flowthrough mode |
| US9150645B2 (en) | 2012-04-20 | 2015-10-06 | Abbvie, Inc. | Cell culture methods to reduce acidic species |
| US9067990B2 (en) | 2013-03-14 | 2015-06-30 | Abbvie, Inc. | Protein purification using displacement chromatography |
| WO2013158273A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Methods to modulate c-terminal lysine variant distribution |
| US9249182B2 (en) | 2012-05-24 | 2016-02-02 | Abbvie, Inc. | Purification of antibodies using hydrophobic interaction chromatography |
| RU2501008C1 (ru) * | 2012-06-14 | 2013-12-10 | Федеральное государственное бюджетное учреждение "Научно-исследовательский институт клинической иммунологии" Сибирского отделения Российской академии медицинских наук (ФГБУ "НИИКИ" СОРАМН) | СПОСОБ АФФИННОГО ВЫДЕЛЕНИЯ АУТОАНТИТЕЛ КЛАССА IgG К ИММУНОРЕГУЛЯТОРНОМУ ЦИТОКИНУ TNF |
| FR2993572B1 (fr) | 2012-07-23 | 2016-04-15 | Emd Millipore Corp | Circuit pour liquide biologique comportant une vanne a pincement |
| AU2013309506A1 (en) | 2012-09-02 | 2015-03-12 | Abbvie Inc. | Methods to control protein heterogeneity |
| US9512214B2 (en) | 2012-09-02 | 2016-12-06 | Abbvie, Inc. | Methods to control protein heterogeneity |
| SG11201501597VA (en) * | 2012-09-03 | 2015-04-29 | Kaneka Corp | Mix-mode antibody affinity separation matrix and purification method using same, and target molecule |
| SG11201404681VA (en) | 2012-09-17 | 2014-09-26 | Grace W R & Co | Chromatography media and devices |
| WO2014077762A1 (en) | 2012-11-13 | 2014-05-22 | Ge Healthcare Bio-Sciences Ab | Multimodal anion exchange matrices |
| JP6639236B2 (ja) | 2013-02-26 | 2020-02-05 | ナトリックス セパレイションズ インコーポレーテッド | 混合モードクロマトグラフィー膜 |
| IL274646B (en) | 2013-03-08 | 2022-09-01 | Genzyme Corp | Integrated continuous production of medicinal substances from medical protein |
| EP2830651A4 (en) | 2013-03-12 | 2015-09-02 | Abbvie Inc | HUMAN ANTIBODIES THAT BIND TNF-ALPHA AND PREPARATION METHODS |
| US10023608B1 (en) * | 2013-03-13 | 2018-07-17 | Amgen Inc. | Protein purification methods to remove impurities |
| US9499614B2 (en) | 2013-03-14 | 2016-11-22 | Abbvie Inc. | Methods for modulating protein glycosylation profiles of recombinant protein therapeutics using monosaccharides and oligosaccharides |
| WO2014159579A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | MUTATED ANTI-TNFα ANTIBODIES AND METHODS OF THEIR USE |
| US9017687B1 (en) | 2013-10-18 | 2015-04-28 | Abbvie, Inc. | Low acidic species compositions and methods for producing and using the same using displacement chromatography |
| US9994609B2 (en) | 2013-03-15 | 2018-06-12 | Biogen Ma Inc. | Hydrophobic interaction protein chromatography under no-salt conditions |
| TWI631132B (zh) * | 2013-05-06 | 2018-08-01 | 賽諾菲公司 | 用於純化抗體之連續多步驟方法 |
| JPWO2015041218A1 (ja) | 2013-09-17 | 2017-03-02 | 株式会社カネカ | 新規抗体精製方法及びそれから得られる抗体(NovelAntibodyPurificationMethodandAntibodyobtainedtherefrom)、並びに陽イオン交換基を用いた新規抗体精製法及びそれから得られる抗体(NovelAntibodyPurificationmethodusingCationExchangerandAntibodyobtainedtherefrom) |
| EP3052640A2 (en) | 2013-10-04 | 2016-08-10 | AbbVie Inc. | Use of metal ions for modulation of protein glycosylation profiles of recombinant proteins |
| US9181337B2 (en) | 2013-10-18 | 2015-11-10 | Abbvie, Inc. | Modulated lysine variant species compositions and methods for producing and using the same |
| US8946395B1 (en) | 2013-10-18 | 2015-02-03 | Abbvie Inc. | Purification of proteins using hydrophobic interaction chromatography |
| US9085618B2 (en) | 2013-10-18 | 2015-07-21 | Abbvie, Inc. | Low acidic species compositions and methods for producing and using the same |
| US20150139988A1 (en) | 2013-11-15 | 2015-05-21 | Abbvie, Inc. | Glycoengineered binding protein compositions |
| EP3698870A1 (en) | 2013-12-12 | 2020-08-26 | EMD Millipore Corporation | Protein separations using an acrylamide containing filter |
| SG11201605712SA (en) | 2014-01-16 | 2016-08-30 | Grace W R & Co | Affinity chromatography media and chromatography devices |
| TWI709570B (zh) | 2014-01-17 | 2020-11-11 | 美商健臻公司 | 無菌層析法及製法 |
| TWI709569B (zh) * | 2014-01-17 | 2020-11-11 | 美商健臻公司 | 無菌層析樹脂及其用於製造方法的用途 |
| EP3094391B1 (en) * | 2014-01-17 | 2024-11-20 | Repligen Corporation | Sterilizing chromatography columns |
| US20240100450A9 (en) * | 2014-01-17 | 2024-03-28 | Repligen Corporation | Sterilizing chromatography columns |
| WO2015138928A2 (en) | 2014-03-14 | 2015-09-17 | Bio-Rad Laboratories, Inc. | Mixed mode ligands |
| CN107847907A (zh) | 2014-05-02 | 2018-03-27 | 格雷斯公司 | 官能化载体材料以及制备和使用官能化载体材料的方法 |
| US10155799B2 (en) * | 2014-07-21 | 2018-12-18 | Merck Sharp & Dohme Corp. | Chromatography process for purification of insulin and insulin analogs |
| TW201628649A (zh) | 2014-10-09 | 2016-08-16 | 再生元醫藥公司 | 減少醫藥調配物中微可見顆粒之方法 |
| CA2966515C (en) | 2014-12-08 | 2021-04-27 | Emd Millipore Corporation | Mixed bed ion exchange adsorber |
| US10695744B2 (en) | 2015-06-05 | 2020-06-30 | W. R. Grace & Co.-Conn. | Adsorbent biprocessing clarification agents and methods of making and using the same |
| WO2017174422A1 (en) * | 2016-04-06 | 2017-10-12 | Ge Healthcare Bioprocess R&D Ab | Chromatography matrix |
| US11020686B2 (en) | 2016-08-16 | 2021-06-01 | Regeneron Pharmaceuticals, Inc. | Methods for quantitating individual antibodies from a mixture |
| BR112019006689A2 (pt) | 2016-10-25 | 2019-06-25 | Regeneron Pharma | métodos e sistemas para análise de dados de cromatografia |
| CN109964123A (zh) * | 2016-11-18 | 2019-07-02 | 捷恩智株式会社 | 抗体的纯化方法 |
| KR20240152951A (ko) | 2017-01-30 | 2024-10-22 | 리제너론 파마슈티칼스 인코포레이티드 | 크로마토그래피에서 바이오버든을 감소시키기 위한 조성물 및 방법 |
| US12042538B2 (en) | 2017-09-19 | 2024-07-23 | Regeneron Pharmaceuticals, Inc. | Methods of reducing particle formation and compositions formed thereby |
| US11534780B2 (en) | 2017-11-14 | 2022-12-27 | General Electric Company | Spray nozzle device for delivering a restorative coating through a hole in a case of a turbine engine |
| US11161128B2 (en) | 2017-11-14 | 2021-11-02 | General Electric Company | Spray nozzle device for delivering a restorative coating through a hole in a case of a turbine engine |
| CN111683976B (zh) | 2018-02-05 | 2022-11-18 | 生物辐射实验室股份有限公司 | 具有阴离子交换-疏水混合模式配体的色谱树脂 |
| WO2019170635A1 (en) | 2018-03-05 | 2019-09-12 | Chiral Technologies Europe Sas | Composite material for bioseparations |
| CN111818981B (zh) | 2018-03-05 | 2022-07-05 | 欧洲手性技术股份公司 | 用于生物分离的复合材料 |
| CN111818980B (zh) | 2018-03-08 | 2022-10-11 | 生物辐射实验室股份有限公司 | 阴离子交换-疏水混合模式色谱树脂 |
| EP3765481A2 (en) * | 2018-03-15 | 2021-01-20 | Klawego GmbH & Co. KG | Composite materials for the depletion of contaminants from solutions |
| EP3546475A1 (en) | 2018-03-27 | 2019-10-02 | Sanofi | Full flow-through process for purifying recombinant proteins |
| TWI853823B (zh) | 2018-07-02 | 2024-09-01 | 美商里珍納龍藥品有限公司 | 自混合物製備多肽之系統及方法 |
| US10737259B2 (en) | 2018-08-31 | 2020-08-11 | Pall Corporation | Salt tolerant anion exchange medium |
| US11045773B2 (en) | 2018-08-31 | 2021-06-29 | Pall Corporation | Salt tolerant porous medium |
| EP3843869A1 (en) | 2018-08-31 | 2021-07-07 | Genzyme Corporation | Sterile chromatography resin and use thereof in manufacturing processes |
| WO2020193483A1 (en) | 2019-03-27 | 2020-10-01 | Cytiva Sweden Ab | A method for separating biomolecules |
| CN113646630B (zh) * | 2019-03-29 | 2024-05-07 | 百时美施贵宝公司 | 测量色谱树脂的疏水性的方法 |
| CN114040815B (zh) | 2019-09-05 | 2024-06-28 | 生物辐射实验室股份有限公司 | 阴离子交换-疏水混合模式色谱树脂 |
| EP4019125A1 (en) | 2020-12-22 | 2022-06-29 | Sartorius Stedim Biotech GmbH | Chromatographic material and method of producing same |
| GB202110014D0 (en) | 2021-07-12 | 2021-08-25 | Cytiva Bioprocess R & D Ab | A method for separating adeno-associated virus capsids, compositions obtained by said method and uses thereof |
| WO2023104770A1 (en) | 2021-12-07 | 2023-06-15 | Cytiva Bioprocess R&D Ab | Separation matrix and methods for separating target molecules |
| GB202202777D0 (en) | 2022-03-01 | 2022-04-13 | Cytiva Bioprocess R & D Ab | A method for separating supercoiled plasmid DNA |
| GB202206123D0 (en) | 2022-04-27 | 2022-06-08 | Cytiva Bioprocess R & D Ab | A pre-screening method and a method for separating adeno-associated virus capsids |
| GB202214280D0 (en) | 2022-09-29 | 2022-11-16 | Cytiva Vioprocess R&D Ab | Chromatography ligand and chromatography material, and uses thereof |
| GB202215814D0 (en) | 2022-10-26 | 2022-12-07 | Cytiva Bioprocess R & D Ab | A chromatography device, system, and use thereof for analytic separation |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2405555A (en) * | 1946-08-13 | Manufacture of heterocyclic bases | ||
| US3467656A (en) * | 1967-09-06 | 1969-09-16 | Hoffmann La Roche | 4-aryl-3,1-benzoxazine-2-thione |
| SE462046C (sv) | 1982-08-23 | 1998-04-27 | Pharmacia Biotech Ab | Hybrid-DNA-vektor innehållande DNA-sekvens från Staphylococcus aureus, förfarande för dess framställning och bakterie innehållande densamma |
| US5151350A (en) * | 1982-10-27 | 1992-09-29 | Repligen Corporation | Cloned genes encoding recombinant protein a |
| US4983722A (en) * | 1988-06-08 | 1991-01-08 | Miles Inc. | Removal of protein A from antibody preparations |
| US5322859A (en) * | 1993-02-08 | 1994-06-21 | University Of Iowa Research Foundation | Antiglaucoma drug composition and method |
| US5429746A (en) * | 1994-02-22 | 1995-07-04 | Smith Kline Beecham Corporation | Antibody purification |
| US5652348A (en) * | 1994-09-23 | 1997-07-29 | Massey University | Chromatographic resins and methods for using same |
| US6117996A (en) * | 1995-09-20 | 2000-09-12 | Novo Nordisk A/S | Triazine based ligands and use thereof |
| GB9519197D0 (en) * | 1995-09-20 | 1995-11-22 | Affinity Chromatography Ltd | Novel affinity ligands and their use |
| SE9601368D0 (sv) * | 1996-04-11 | 1996-04-11 | Pharmacia Biotech Ab | Process for the production of a porous cross-linked polysaccharide gel |
| AU729039C (en) * | 1996-08-30 | 2001-08-02 | Upfront Chromatography A/S | Isolation of immunoglobulins |
| SE9700383D0 (sv) * | 1997-02-04 | 1997-02-04 | Pharmacia Biotech Ab | An adsorption/separation method and a medium for adsorption/separation |
| US5908960A (en) * | 1997-05-07 | 1999-06-01 | Smithkline Beecham Corporation | Compounds |
| ES2364086T3 (es) * | 1999-07-07 | 2011-08-24 | Zymogenetics, Inc. | Receptor de citoquina humana. |
| SE9904197D0 (sv) * | 1999-11-22 | 1999-11-22 | Amersham Pharm Biotech Ab | A method for anion exchange adsorption on matrices carrying mixed mode ligands |
| EP1288198B1 (en) * | 2000-06-08 | 2006-12-20 | Kaneka Corporation | Process for the production of sulfonic esters |
| SE0004932D0 (sv) | 2000-12-31 | 2000-12-31 | Apbiotech Ab | A method for mixed mode adsorption and mixed mode adsorbents |
| WO2002053256A1 (en) * | 2001-01-05 | 2002-07-11 | Pro-Chem, Inc. | Devices and methods for purification |
| US6652853B2 (en) * | 2001-03-08 | 2003-11-25 | Ludwig Institute For Cancer Research | Method for treating cancer using A33 specific antibodies and chemotherapeutic agents |
| DE10155984A1 (de) | 2001-11-15 | 2003-05-28 | Boehringer Ingelheim Pharma | Verfahren zur Reduktion des Liganden-leakage von Affinitätschromatographie-Matrices |
| DK1601697T3 (da) * | 2003-02-28 | 2007-10-01 | Lonza Biologics Plc | Oprensning af antistof ved protein A- og ionbytningskromatografi |
| CA2552639C (en) * | 2004-02-27 | 2012-05-01 | Ge Healthcare Bio-Sciences Ab | A process for the purification of antibodies |
| EP1793926B1 (en) | 2004-09-22 | 2016-11-23 | GE Healthcare BioProcess R&D AB | Method of preparing a chromatography matrix |
| US9266041B2 (en) * | 2004-10-21 | 2016-02-23 | Ge Healthcare Bio-Sciences Ab | Chromatography ligand |
| JP4831436B2 (ja) * | 2004-10-21 | 2011-12-07 | ジーイー・ヘルスケア・バイオサイエンス・アクチボラグ | クロマトグラフィーリガンド |
| US7691980B2 (en) * | 2007-01-09 | 2010-04-06 | Bio-Rad Laboratories, Inc. | Enhanced capacity and purification of antibodies by mixed mode chromatography in the presence of aqueous-soluble nonionic organic polymers |
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