PL215170B1 - Sposób wytwarzania rozpuszczalnego kompleksu zawierajacego amyloidogenne bialko docelowe oraz bialko opiekuncze z klasy izomeraz peptydyloprolilowych - Google Patents
Sposób wytwarzania rozpuszczalnego kompleksu zawierajacego amyloidogenne bialko docelowe oraz bialko opiekuncze z klasy izomeraz peptydyloprolilowychInfo
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- PL215170B1 PL215170B1 PL367679A PL36767902A PL215170B1 PL 215170 B1 PL215170 B1 PL 215170B1 PL 367679 A PL367679 A PL 367679A PL 36767902 A PL36767902 A PL 36767902A PL 215170 B1 PL215170 B1 PL 215170B1
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- Prior art keywords
- hiv
- protein
- chaperone
- leu
- fkpa
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| HUE037408T2 (hu) | 2011-06-10 | 2018-08-28 | Univ Oregon Health & Science | CMV glikoproteinek és rekombináns vektorok |
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| AR093778A1 (es) | 2012-11-08 | 2015-06-24 | Hoffmann La Roche | PROTEINAS LIGANTES DE ANTIGENO ANTI-HER3/HER4 DE UNION A LA HORQUILLA b DE HER3 Y A LA HORQUILLA b DE HER4 |
| MA38165A1 (fr) | 2012-11-08 | 2018-07-31 | Hoffmann La Roche | Protéines de liaison à l'antigène her3 se liant à l'épingle à cheveux beta de her3 |
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| MX2016014416A (es) | 2014-05-14 | 2017-02-23 | Hoffmann La Roche | Anticuerpos anti-her3 que se unen a la horquilla beta de her3. |
| BR112016025056A2 (pt) | 2014-05-14 | 2018-02-20 | F. Hoffmann-La Roche Ag | uso de pelo menos um polipeptídeo, anticorpo biespecífico, anticorpo biespecífico isolado, anticorpo her3/her2 biespecífico, célula hospedeira, método de produção do anticorpo biespecífico her3/her2, imunoconjugado e formulação farmacêutica |
| CN107532190B (zh) | 2014-12-01 | 2021-07-09 | 菲尼克斯公司 | 用于肽生产的融合伴侣 |
| CA2974343A1 (en) * | 2015-02-13 | 2016-08-18 | Sekisui Chemical Co., Ltd. | Nucleic acid, fusion protein, recombined cell, and isoprene or cyclic terpene production method |
| EP3069730A3 (en) | 2015-03-20 | 2017-03-15 | International Aids Vaccine Initiative | Soluble hiv-1 envelope glycoprotein trimers |
| US9931394B2 (en) | 2015-03-23 | 2018-04-03 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
| JP6967002B2 (ja) * | 2015-12-15 | 2021-11-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | トランスグルタミナーゼ認識部位を有するfkbpドメイン |
| ES2796479T3 (es) | 2016-05-31 | 2020-11-27 | Hoffmann La Roche | Procedimiento de pretratamiento para la detección rápida del antígeno central del VHC |
| JP2019523863A (ja) | 2016-05-31 | 2019-08-29 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ウイルス抗原の血清学的検出方法 |
| EP3472322B1 (en) * | 2016-06-20 | 2022-01-05 | MetGen Oy | Method for obtaining active insoluble xylose isomerase |
| JP7068323B2 (ja) | 2017-02-02 | 2022-05-16 | エフ.ホフマン-ラ ロシュ アーゲー | 少なくとも2種のペグ化された分析物特異的結合剤を使用する免疫アッセイ |
| CN110709410B (zh) | 2017-04-26 | 2024-07-02 | 豪夫迈·罗氏有限公司 | 可溶性和免疫反应性寨卡病毒ns1多肽 |
| CN110996986B (zh) | 2017-07-27 | 2024-07-19 | 豪夫迈·罗氏有限公司 | Hcv抗原的多表位融合蛋白及其用途 |
| CN110066343B (zh) * | 2019-05-23 | 2021-04-09 | 北京新创生物工程有限公司 | 一种用于检测hiv新发感染的重组抗原及其应用 |
| CN115843334B (zh) | 2020-04-23 | 2026-01-13 | 豪夫迈·罗氏有限公司 | 用于抗体免疫测定的冠状核衣壳抗原 |
| WO2023012321A1 (en) | 2021-08-06 | 2023-02-09 | Roche Diagnostics Gmbh | Chimeric igg-fc-binding ligand polypeptide and uses thereof for igg affinity purification |
| US20250298022A1 (en) | 2022-05-03 | 2025-09-25 | Roche Diagnostics Operations, Inc. | Hiv gp41 variants for immunodiagnostic assays |
| WO2025098623A1 (en) | 2023-11-09 | 2025-05-15 | Roche Diagnostics Gmbh | Transglutaminase substrates for labeling |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2095818B (en) | 1981-03-27 | 1985-10-02 | Exxon Research Engineering Co | Staged adsorption/resorption heat pump |
| US4735896A (en) | 1986-03-04 | 1988-04-05 | United Biomedical, Inc. | Synthetic peptide and process of using same for the detection and diagnosis of AIDS and pre-AIDS conditions |
| US4879212A (en) | 1986-04-02 | 1989-11-07 | United Biomedical Inc. | Peptide composition and method for the detection of antibodies to HTLV-III |
| US6024983A (en) | 1986-10-24 | 2000-02-15 | Southern Research Institute | Composition for delivering bioactive agents for immune response and its preparation |
| DE3705686C2 (de) | 1987-02-23 | 1995-11-30 | Boehringer Mannheim Gmbh | Verfahren zur Bestimmung von Antikörpern |
| NZ224663A (en) | 1987-05-28 | 1990-11-27 | Amrad Corp Ltd | Fusion proteins containing glutathione-s-transferase and expression of foreign polypeptides using glutathione-s-transferase encoding vectors |
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| CA2003383A1 (en) * | 1988-11-23 | 1990-05-23 | Sushil G. Devare | Synthetic dna derived recombinant hiv antigens |
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| WO1993013200A1 (en) * | 1991-12-20 | 1993-07-08 | Novo Nordisk A/S | A process for the preparation of lipase |
| JP2001504572A (ja) | 1992-04-09 | 2001-04-03 | アボツト・ラボラトリーズ | Hiv抗原及びhiv抗体を検出するためのアッセイ |
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| ATE195347T1 (de) | 1992-10-02 | 2000-08-15 | Res Corp Technologies Inc | Methoden der erhöhung der sekretion von überexpremierten proteinen |
| US5459051A (en) | 1993-03-26 | 1995-10-17 | Celtrix Pharmaceuticals, Inc. | Methods and vectors for over-expression of ubiquitin fusion proteins in host cells |
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| AU3968595A (en) | 1994-10-25 | 1996-05-15 | Board Of Trustees Of The Leland Stanford Junior University | Conditional transformation of genetically engineered cells |
| WO1996041865A1 (en) | 1995-06-07 | 1996-12-27 | Ariad Gene Therapeutics, Inc. | Rapamcycin-based regulation of biological events |
| WO1997010502A1 (en) | 1995-09-15 | 1997-03-20 | Merck & Co., Inc. | A high throughput assay using fusion proteins |
| US5723125A (en) * | 1995-12-28 | 1998-03-03 | Tanox Biosystems, Inc. | Hybrid with interferon-alpha and an immunoglobulin Fc linked through a non-immunogenic peptide |
| GB9614114D0 (en) | 1996-07-05 | 1996-09-04 | Amcor Packaging Uk Ltd | New packages |
| JP2001501093A (ja) | 1996-09-26 | 2001-01-30 | メディカル リサーチ カウンシル | シャペロン断片 |
| US6225082B1 (en) * | 1997-05-09 | 2001-05-01 | Research Corporation Technologies, Inc. | Myelin basic protein MRNA transport and translation enhancer sequences |
| US5989868A (en) * | 1997-09-12 | 1999-11-23 | The Board Of Regents Of The University Of Oklahoma | Fusion protein systems designed to increase soluble cytoplasmic expression of heterologous proteins in esherichia coli |
| JP2002508971A (ja) | 1998-01-15 | 2002-03-26 | アリアド・ジーン・セラピューティクス・インコーポレーテッド | 多量体キメラ蛋白質を使用する生物学的イベントの調節 |
| DE19913117A1 (de) * | 1998-05-06 | 1999-11-11 | Roche Diagnostics Gmbh | Entstörung durch Rheumafaktoren |
| US6248329B1 (en) * | 1998-06-01 | 2001-06-19 | Ramaswamy Chandrashekar | Parasitic helminth cuticlin nucleic acid molecules and uses thereof |
| ATE473755T1 (de) | 1998-10-02 | 2010-07-15 | Rhein Biotech Proz & Prod Gmbh | Methode zur herstellung von (poly)peptiden unter verwendung von verkürzten varianten von sv40 large t antigen mit einem intakten n terminus |
| EP1127140A2 (en) | 1998-11-06 | 2001-08-29 | President And Fellows Of Harvard College | Fk506-based regulation of biological events |
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| AU4933200A (en) | 1999-05-14 | 2000-12-05 | Medical Research Council | Oligomeric chaperone proteins |
| GB9913437D0 (en) | 1999-06-09 | 1999-08-11 | Medical Res Council | Fusion proteins |
| EP1077263A1 (de) * | 1999-07-29 | 2001-02-21 | F.Hoffmann-La Roche Ag | Verfahren zur Herstellung von natürlich gefalteten und sekretierten Proteinen durch Co-Sekretion von Chaperonen |
| CA2403718A1 (en) * | 2000-03-17 | 2001-09-27 | Panacos Pharmaceuticals, Inc. | A method for generating immunogens that elicit neutralizing antibodies against fusion-active regions of hiv envelope proteins |
| JP2002262883A (ja) * | 2001-03-13 | 2002-09-17 | Sekisui Chem Co Ltd | モノクローナル抗体の製造方法 |
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