JP2004516928A5 - - Google Patents
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- JP2004516928A5 JP2004516928A5 JP2002554197A JP2002554197A JP2004516928A5 JP 2004516928 A5 JP2004516928 A5 JP 2004516928A5 JP 2002554197 A JP2002554197 A JP 2002554197A JP 2002554197 A JP2002554197 A JP 2002554197A JP 2004516928 A5 JP2004516928 A5 JP 2004516928A5
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- 239000003446 ligand Substances 0.000 description 288
- 239000000126 substance Substances 0.000 description 117
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- 150000002500 ions Chemical class 0.000 description 52
- 230000003993 interaction Effects 0.000 description 49
- 238000001179 sorption measurement Methods 0.000 description 48
- 229920002684 Sepharose Polymers 0.000 description 43
- 238000005342 ion exchange Methods 0.000 description 41
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- 150000003839 salts Chemical class 0.000 description 36
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 35
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- 239000000872 buffer Substances 0.000 description 33
- 238000006467 substitution reaction Methods 0.000 description 33
- -1 sulfopropyl groups Chemical group 0.000 description 31
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 30
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- 239000002585 base Substances 0.000 description 26
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| SE0004932A SE0004932D0 (sv) | 2000-12-31 | 2000-12-31 | A method for mixed mode adsorption and mixed mode adsorbents |
| PCT/EP2001/014895 WO2002053252A2 (en) | 2000-12-31 | 2001-12-17 | A method for mixed mode adsorption and mixed mode adsorbents |
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Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6908770B1 (en) * | 1998-07-16 | 2005-06-21 | Board Of Regents, The University Of Texas System | Fluid based analysis of multiple analytes by a sensor array |
| US7173003B2 (en) | 2001-10-10 | 2007-02-06 | Neose Technologies, Inc. | Granulocyte colony stimulating factor: remodeling and glycoconjugation of G-CSF |
| US7214660B2 (en) * | 2001-10-10 | 2007-05-08 | Neose Technologies, Inc. | Erythropoietin: remodeling and glycoconjugation of erythropoietin |
| US20060228256A1 (en) * | 2003-02-07 | 2006-10-12 | Board Of Regents, The University Of Texas System | Multi-shell microspheres with integrated chomatographic and detection layers for use in array sensors |
| EP2055189A1 (en) | 2003-04-09 | 2009-05-06 | Neose Technologies, Inc. | Glycopegylation methods and proteins/peptides produced by the methods |
| US7943393B2 (en) * | 2003-07-14 | 2011-05-17 | Phynexus, Inc. | Method and device for extracting an analyte |
| WO2005012484A2 (en) | 2003-07-25 | 2005-02-10 | Neose Technologies, Inc. | Antibody-toxin conjugates |
| GB2407783A (en) * | 2003-11-07 | 2005-05-11 | Novexin Ltd | Chromatographic separation |
| US20080305992A1 (en) | 2003-11-24 | 2008-12-11 | Neose Technologies, Inc. | Glycopegylated erythropoietin |
| US8105849B2 (en) * | 2004-02-27 | 2012-01-31 | Board Of Regents, The University Of Texas System | Integration of fluids and reagents into self-contained cartridges containing sensor elements |
| US8101431B2 (en) * | 2004-02-27 | 2012-01-24 | Board Of Regents, The University Of Texas System | Integration of fluids and reagents into self-contained cartridges containing sensor elements and reagent delivery systems |
| WO2006010143A2 (en) | 2004-07-13 | 2006-01-26 | Neose Technologies, Inc. | Branched peg remodeling and glycosylation of glucagon-like peptide-1 [glp-1] |
| KR101243601B1 (ko) | 2004-10-21 | 2013-03-20 | 지이 헬스케어 바이오-사이언시스 에이비 | 크로마토그래피 리간드 |
| US20080176790A1 (en) | 2004-10-29 | 2008-07-24 | Defrees Shawn | Remodeling and Glycopegylation of Fibroblast Growth Factor (Fgf) |
| EP1693108A1 (en) | 2004-12-04 | 2006-08-23 | MERCK PATENT GmbH | Mixed-modal anion-exchange type separation material |
| US9029331B2 (en) * | 2005-01-10 | 2015-05-12 | Novo Nordisk A/S | Glycopegylated granulocyte colony stimulating factor |
| US20070154992A1 (en) * | 2005-04-08 | 2007-07-05 | Neose Technologies, Inc. | Compositions and methods for the preparation of protease resistant human growth hormone glycosylation mutants |
| WO2006127973A2 (en) * | 2005-05-24 | 2006-11-30 | Waters Inverstments Limited | Methods for separating and analyzing anionic compounds |
| WO2007053186A2 (en) | 2005-05-31 | 2007-05-10 | Labnow, Inc. | Methods and compositions related to determination and use of white blood cell counts |
| US20070105755A1 (en) * | 2005-10-26 | 2007-05-10 | Neose Technologies, Inc. | One pot desialylation and glycopegylation of therapeutic peptides |
| WO2007056191A2 (en) | 2005-11-03 | 2007-05-18 | Neose Technologies, Inc. | Nucleotide sugar purification using membranes |
| WO2007092827A2 (en) | 2006-02-08 | 2007-08-16 | Waters Investments Limited | Improved separation method |
| CA2655873C (en) | 2006-07-14 | 2017-10-17 | Wisconsin Alumni Research Foundation | Adsorptive membranes for trapping viruses |
| ES2516694T3 (es) * | 2006-07-21 | 2014-10-31 | Ratiopharm Gmbh | Glicosilación de péptidos a través de secuencias de glicosilación con unión en O |
| US8969532B2 (en) * | 2006-10-03 | 2015-03-03 | Novo Nordisk A/S | Methods for the purification of polypeptide conjugates comprising polyalkylene oxide using hydrophobic interaction chromatography |
| US20100041872A1 (en) * | 2006-10-04 | 2010-02-18 | Defrees Shawn | Glycerol linked pegylated sugars and glycopeptides |
| WO2008073620A2 (en) * | 2006-11-02 | 2008-06-19 | Neose Technologies, Inc. | Manufacturing process for the production of polypeptides expressed in insect cell-lines |
| 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 |
| KR20100016160A (ko) * | 2007-04-03 | 2010-02-12 | 바이오제너릭스 에이지 | 글리코페길화 ｇ―ｃｓｆ를 이용하는 치료 방법 |
| WO2008154639A2 (en) | 2007-06-12 | 2008-12-18 | Neose Technologies, Inc. | Improved process for the production of nucleotide sugars |
| CA2693334C (en) * | 2007-07-25 | 2015-07-07 | Ge Healthcare Bio-Sciences Ab | Separation matrix |
| CA2711503A1 (en) * | 2008-01-08 | 2009-07-16 | Biogenerix Ag | Glycoconjugation of polypeptides using oligosaccharyltransferases |
| KR101582841B1 (ko) | 2008-02-27 | 2016-01-11 | 노보 노르디스크 에이/에스 | 콘쥬게이트된 인자 ｖｉｉｉ 분자 |
| US8188242B2 (en) | 2008-04-08 | 2012-05-29 | Bio-Rad Laboratories, Inc. | Chromatography purification of antibodies |
| EP2459308A1 (en) * | 2009-07-28 | 2012-06-06 | instrAction GmbH | Specific sorbent for binding proteins and peptides, and separation method using the same |
| WO2011046494A1 (en) * | 2009-10-12 | 2011-04-21 | Ge Healthcare Bio-Sciences Ab | Separation matrices |
| JP5560347B2 (ja) | 2009-12-07 | 2014-07-23 | フレセニウス メディカル ケア ホールディングス インコーポレーテッド | ジルコニウムイオン交換収着剤を用いた浄水カートリッジ |
| MX2012006983A (es) * | 2009-12-17 | 2013-02-06 | Instraction Gmbh | Absorbente especifico para unir proteinas y peptidos, y metodo de separacion que utiliza el mismo. |
| EP2674753B1 (en) * | 2011-02-10 | 2020-05-13 | Sekisui Medical Co., Ltd. | Method for separating and detecting a nucleic acid strand |
| JP2012211110A (ja) * | 2011-03-31 | 2012-11-01 | Asahi Kasei Medical Co Ltd | 多孔質吸着膜 |
| EP2570181A1 (en) * | 2011-09-15 | 2013-03-20 | InstrAction GmbH | Sorbent comprising its surface an aliphatic unit having an anionic or deprotonizable group for the purfication of organic molecules |
| CN107754776B (zh) | 2012-05-15 | 2021-09-21 | 沃特世科技公司 | 色谱材料 |
| CN104487447B (zh) * | 2012-05-31 | 2018-10-30 | 新加坡科技研究局 | 用于降低蛋白制剂领域中的聚集物含量的混合的多官能性金属亲和表面 |
| RU2015114330A (ru) | 2012-09-17 | 2016-11-10 | У.Р. Грейс Энд Ко.-Конн. | Хроматографические среды и устройства |
| WO2014043644A1 (en) * | 2012-09-17 | 2014-03-20 | Alltech Associates, Inc. | Functionalized particulate support material and methods of making and using the same |
| JP2016513245A (ja) * | 2013-02-06 | 2016-05-12 | エイジェンシー・フォー・サイエンス，テクノロジー・アンド・リサーチ | タンパク質製剤の凝集体含有量を減少させる混合多官能金属親和性表面 |
| US10023608B1 (en) | 2013-03-13 | 2018-07-17 | Amgen Inc. | Protein purification methods to remove impurities |
| US11229896B2 (en) | 2014-01-16 | 2022-01-25 | W.R. Grace & Co.—Conn. | Affinity chromatography media and chromatography devices |
| JP6914189B2 (ja) | 2014-05-02 | 2021-08-04 | ダブリュー・アール・グレース・アンド・カンパニー−コーンＷ Ｒ Ｇｒａｃｅ ＆ Ｃｏ−Ｃｏｎｎ | 官能化担体材料並びに官能化担体材料を作製及び使用する方法 |
| CN107921407B (zh) | 2015-06-05 | 2022-07-05 | 格雷斯公司 | 生物处理吸附澄清剂及其制备和使用方法 |
| CN110844886A (zh) * | 2019-12-02 | 2020-02-28 | 锦西化工研究院有限公司 | 一种二硫化钠水溶液的合成方法 |
| CN111617747B (zh) * | 2020-05-11 | 2022-05-31 | 贵州大学 | 一种壳聚糖/纳米金属复合水凝胶及其制备方法和应用 |
| EP4308176A4 (en) * | 2021-03-17 | 2025-02-19 | Bio-Rad Laboratories, Inc. | MIXED-MODE CATION EXCHANGE CHROMATOGRAPHY LIGANDS BASED ON 1,3-DIOXOISOINDOLIN-2-YL STRUCTURES |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4767670A (en) * | 1987-01-21 | 1988-08-30 | E. I. Du Pont De Nemours And Company | Chromatographic supports for separation of oligonucleotides |
| JPH0564748A (ja) * | 1991-09-06 | 1993-03-19 | Tosoh Corp | イオン交換体 |
| US5652348A (en) * | 1994-09-23 | 1997-07-29 | Massey University | Chromatographic resins and methods for using same |
| SE9600590D0 (sv) | 1996-02-19 | 1996-02-19 | Pharmacia Biotech Ab | Sätt för kromatografisk separation av peptider och nukleinsyra samt ny högaffin jonbytesmatris |
| SE9802214D0 (sv) * | 1998-06-18 | 1998-06-18 | Amersham Pharm Biotech Ab | Jonbytare och användning därav |
| US6310199B1 (en) * | 1999-05-14 | 2001-10-30 | Promega Corporation | pH dependent ion exchange matrix and method of use in the isolation of nucleic acids |
| SE9904197D0 (sv) | 1999-11-22 | 1999-11-22 | Amersham Pharm Biotech Ab | A method for anion exchange adsorption on matrices carrying mixed mode ligands |
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- 2001-12-17 CA CA2431012A patent/CA2431012C/en not_active Expired - Lifetime
- 2001-12-17 EP EP01985893A patent/EP1345695A2/en not_active Withdrawn
- 2001-12-17 US US10/451,192 patent/US7008542B2/en not_active Expired - Lifetime
- 2001-12-17 WO PCT/EP2001/014895 patent/WO2002053252A2/en not_active Ceased
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