DE60017083T2 - Einfaches verfahren zur herstellung von markierten konjugaten - Google Patents
Einfaches verfahren zur herstellung von markierten konjugaten Download PDFInfo
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- DE60017083T2 DE60017083T2 DE60017083T DE60017083T DE60017083T2 DE 60017083 T2 DE60017083 T2 DE 60017083T2 DE 60017083 T DE60017083 T DE 60017083T DE 60017083 T DE60017083 T DE 60017083T DE 60017083 T2 DE60017083 T2 DE 60017083T2
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- 239000005090 green fluorescent protein Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000003018 immunoassay Methods 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000002523 lectin Substances 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 108700041430 link Proteins 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000002751 oligonucleotide probe Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- RXNXLAHQOVLMIE-UHFFFAOYSA-N phenyl 10-methylacridin-10-ium-9-carboxylate Chemical compound C12=CC=CC=C2[N+](C)=C2C=CC=CC2=C1C(=O)OC1=CC=CC=C1 RXNXLAHQOVLMIE-UHFFFAOYSA-N 0.000 description 1
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 108010004335 phycoerythrocyanin Proteins 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 238000011533 pre-incubation Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012460 protein solution Substances 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 108010054624 red fluorescent protein Proteins 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 150000003335 secondary amines Chemical group 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical class [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 108091005957 yellow fluorescent proteins Proteins 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/531—Production of immunochemical test materials
- G01N33/532—Production of labelled immunochemicals
Landscapes
- Health & Medical Sciences (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Pathology (AREA)
- Peptides Or Proteins (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11668999P | 1999-01-22 | 1999-01-22 | |
| US116689P | 1999-01-22 | ||
| PCT/US2000/001350 WO2000043784A1 (en) | 1999-01-22 | 2000-01-21 | Simple method for labeled conjugate production |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60017083D1 DE60017083D1 (de) | 2005-02-03 |
| DE60017083T2 true DE60017083T2 (de) | 2005-12-22 |
Family
ID=22368643
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60017083T Expired - Lifetime DE60017083T2 (de) | 1999-01-22 | 2000-01-21 | Einfaches verfahren zur herstellung von markierten konjugaten |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP1145007B1 (enExample) |
| JP (1) | JP4731018B2 (enExample) |
| AT (1) | ATE286250T1 (enExample) |
| AU (1) | AU771248B2 (enExample) |
| CA (1) | CA2359234C (enExample) |
| DE (1) | DE60017083T2 (enExample) |
| WO (1) | WO2000043784A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005015212A1 (en) * | 2003-08-07 | 2005-02-17 | Cellfree Sciences Co., Ltd. | Reagent for producing a protein chip |
| GB2478359B (en) * | 2010-03-05 | 2018-09-12 | Innova Biosciences Ltd | Conjugation reactions |
| US8877892B2 (en) | 2011-03-15 | 2014-11-04 | Innova Biosciences Limited | Conjugation reactions |
| JP2017083461A (ja) * | 2016-12-21 | 2017-05-18 | イノーバ・バイオサイエンシズ・リミテッドＩｎｎｏｖａ Ｂｉｏｓｃｉｅｎｃｅｓ Ｌｔｄ | 共役反応 |
| CN109490298B (zh) * | 2018-12-04 | 2021-02-02 | 郑州大学 | 一种可视化偶联反应试剂盒 |
| CN110108868B (zh) * | 2019-05-27 | 2022-09-06 | 蓝怡科技集团股份有限公司 | 一种酶标记的方法及其应用 |
| CN111044732A (zh) * | 2019-12-27 | 2020-04-21 | 桂林优利特医疗电子有限公司 | 用于流式细胞仪法cd45抗原检测的试剂盒及其制备方法 |
| CN114354950A (zh) * | 2022-01-18 | 2022-04-15 | 北京易斯威特生物科技股份有限公司 | 一种性激素功能联合检测用试纸条、制备方法及其应用 |
| CN114539368B (zh) * | 2022-02-16 | 2023-08-29 | 上海万子健生物科技有限公司 | 一种链霉亲和素藻红蛋白冻干粉的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4732864A (en) * | 1983-10-06 | 1988-03-22 | E. I. Du Pont De Nemours And Company | Trace-labeled conjugates of metallothionein and target-seeking biologically active molecules |
| US5202451A (en) * | 1988-02-17 | 1993-04-13 | Neorx Corporation | Anchimeric radiometal chelating compounds |
| JP2731613B2 (ja) * | 1989-12-12 | 1998-03-25 | 株式会社クラレ | 酵素免疫測定用カートリツジ、それを用いた測定方法及び測定装置 |
| CA2168283A1 (en) * | 1996-01-29 | 1997-07-30 | John Michael Lee | Preparation of biological material for implants |
| US6159698A (en) * | 1996-07-18 | 2000-12-12 | Dade Behring Marburg Gmbh | Reagents for assays for mycophenolic acid |
-
2000
- 2000-01-21 DE DE60017083T patent/DE60017083T2/de not_active Expired - Lifetime
- 2000-01-21 CA CA2359234A patent/CA2359234C/en not_active Expired - Fee Related
- 2000-01-21 AU AU25118/00A patent/AU771248B2/en not_active Ceased
- 2000-01-21 EP EP00903358A patent/EP1145007B1/en not_active Expired - Lifetime
- 2000-01-21 AT AT00903358T patent/ATE286250T1/de not_active IP Right Cessation
- 2000-01-21 WO PCT/US2000/001350 patent/WO2000043784A1/en not_active Ceased
- 2000-01-21 JP JP2000595154A patent/JP4731018B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2359234A1 (en) | 2000-07-27 |
| EP1145007B1 (en) | 2004-12-29 |
| DE60017083D1 (de) | 2005-02-03 |
| AU771248B2 (en) | 2004-03-18 |
| JP4731018B2 (ja) | 2011-07-20 |
| EP1145007A1 (en) | 2001-10-17 |
| JP2002535657A (ja) | 2002-10-22 |
| CA2359234C (en) | 2011-11-15 |
| WO2000043784A1 (en) | 2000-07-27 |
| ATE286250T1 (de) | 2005-01-15 |
| AU2511800A (en) | 2000-08-07 |
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|---|---|---|---|
| 8364 | No opposition during term of opposition |