JPS6172797A - 合成オリゴヌクレオチド類の精製方法 - Google Patents
合成オリゴヌクレオチド類の精製方法Info
- Publication number
- JPS6172797A JPS6172797A JP60201877A JP20187785A JPS6172797A JP S6172797 A JPS6172797 A JP S6172797A JP 60201877 A JP60201877 A JP 60201877A JP 20187785 A JP20187785 A JP 20187785A JP S6172797 A JPS6172797 A JP S6172797A
- Authority
- JP
- Japan
- Prior art keywords
- oligonucleotides
- carrier
- adsorbed
- solution
- eluted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 108091034117 Oligonucleotide Proteins 0.000 title claims abstract description 28
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 238000000746 purification Methods 0.000 title abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 21
- 125000006239 protecting group Chemical group 0.000 claims abstract description 13
- 238000003776 cleavage reaction Methods 0.000 claims abstract description 6
- 230000007017 scission Effects 0.000 claims abstract description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 24
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- 239000001913 cellulose Substances 0.000 claims description 7
- 229920002678 cellulose Polymers 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 238000005342 ion exchange Methods 0.000 claims description 6
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 5
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 5
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 claims description 4
- AFQIYTIJXGTIEY-UHFFFAOYSA-N hydrogen carbonate;triethylazanium Chemical compound OC(O)=O.CCN(CC)CC AFQIYTIJXGTIEY-UHFFFAOYSA-N 0.000 claims description 4
- -1 polytetrafluoroethylene Polymers 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 238000010828 elution Methods 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229960005215 dichloroacetic acid Drugs 0.000 claims description 2
- 238000001179 sorption measurement Methods 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 4
- 239000007853 buffer solution Substances 0.000 claims 3
- 238000001704 evaporation Methods 0.000 claims 1
- 230000008020 evaporation Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 125000003729 nucleotide group Chemical group 0.000 description 14
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 14
- 239000002773 nucleotide Substances 0.000 description 13
- 239000000126 substance Substances 0.000 description 6
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 239000012634 fragment Substances 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000010511 deprotection reaction Methods 0.000 description 3
- 238000011033 desalting Methods 0.000 description 3
- 238000006642 detritylation reaction Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001962 electrophoresis Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- UUTKICFRNVKFRG-WDSKDSINSA-N (4R)-3-[oxo-[(2S)-5-oxo-2-pyrrolidinyl]methyl]-4-thiazolidinecarboxylic acid Chemical compound OC(=O)[C@@H]1CSCN1C(=O)[C@H]1NC(=O)CC1 UUTKICFRNVKFRG-WDSKDSINSA-N 0.000 description 1
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- GUBGYTABKSRVRQ-WFVLMXAXSA-N DEAE-cellulose Chemical compound OC1C(O)C(O)C(CO)O[C@H]1O[C@@H]1C(CO)OC(O)C(O)C1O GUBGYTABKSRVRQ-WFVLMXAXSA-N 0.000 description 1
- 230000006820 DNA synthesis Effects 0.000 description 1
- 241000220324 Pyrus Species 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- QRMKTNANRJCRCY-UHFFFAOYSA-N ethylammonium acetate Chemical compound CC[NH3+].CC([O-])=O QRMKTNANRJCRCY-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 238000002515 oligonucleotide synthesis Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 235000021017 pears Nutrition 0.000 description 1
- 150000004713 phosphodiesters Chemical class 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Saccharide Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19843433649 DE3433649A1 (de) | 1984-09-13 | 1984-09-13 | Verfahren zur aufreinigung synthetischer oligonucleotide |
| DE3433649.4 | 1984-09-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6172797A true JPS6172797A (ja) | 1986-04-14 |
| JPH0556359B2 JPH0556359B2 (en:Method) | 1993-08-19 |
Family
ID=6245325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60201877A Granted JPS6172797A (ja) | 1984-09-13 | 1985-09-13 | 合成オリゴヌクレオチド類の精製方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4997927A (en:Method) |
| EP (1) | EP0174525B1 (en:Method) |
| JP (1) | JPS6172797A (en:Method) |
| AT (1) | ATE55392T1 (en:Method) |
| CA (1) | CA1288363C (en:Method) |
| DE (2) | DE3433649A1 (en:Method) |
| DK (1) | DK174507B1 (en:Method) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11127854A (ja) * | 1997-10-28 | 1999-05-18 | Hitachi Ltd | 核酸の回収方法及び装置 |
| JPH11266864A (ja) * | 1998-03-19 | 1999-10-05 | Hitachi Ltd | 核酸の精製方法および精製用装置 |
| JP2000166556A (ja) * | 1998-12-10 | 2000-06-20 | Hitachi Ltd | 核酸の回収方法及び装置 |
| JP2002191351A (ja) * | 2001-10-19 | 2002-07-09 | Hitachi Ltd | 核酸の精製用装置および核酸捕捉用チップ |
| JP2004298195A (ja) * | 2004-07-09 | 2004-10-28 | Hitachi Ltd | 核酸の回収方法 |
| JP2005538116A (ja) * | 2002-08-02 | 2005-12-15 | シクロプス ゲノム サイエンス リミテッド | 核酸の安定化 |
| JP2007330271A (ja) * | 2007-09-21 | 2007-12-27 | Hitachi Ltd | 核酸の回収方法 |
| JP2019518759A (ja) * | 2016-06-14 | 2019-07-04 | バイオジェン・エムエイ・インコーポレイテッドＢｉｏｇｅｎ ＭＡ Ｉｎｃ． | オリゴヌクレオチドの精製のための疎水性相互作用クロマトグラフィー |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3433649A1 (de) * | 1984-09-13 | 1986-03-20 | Gesellschaft für Biotechnologische Forschung mbH (GBF), 3300 Braunschweig | Verfahren zur aufreinigung synthetischer oligonucleotide |
| US5262530A (en) | 1988-12-21 | 1993-11-16 | Applied Biosystems, Inc. | Automated system for polynucleotide synthesis and purification |
| US5047524A (en) * | 1988-12-21 | 1991-09-10 | Applied Biosystems, Inc. | Automated system for polynucleotide synthesis and purification |
| WO1996003417A1 (en) * | 1994-07-25 | 1996-02-08 | Hybridon, Inc. | Improved methods of detritylation for oligonucleotide synthesis |
| SE9500183D0 (sv) * | 1995-01-20 | 1995-01-20 | Pharmacia Biotech Ab | Method for the purifivation of short nucleic acids |
| WO1998035753A1 (de) * | 1997-02-17 | 1998-08-20 | GESELLSCHAFT FüR BIOTECHNOLOGISCHE FORSCHUNG MBH (GBF) | Vorrichtung für eine automatisierte chemische synthese |
| US6177559B1 (en) * | 1998-04-24 | 2001-01-23 | Transgenomic, Inc. | Process for separation of polynucleotide fragments |
| US5986085A (en) * | 1997-04-25 | 1999-11-16 | Transgenomic, Inc. | Matched ion polynucleotide chromatography (MIPC) process for separation of polynucleotide fragments |
| US6265168B1 (en) | 1998-10-06 | 2001-07-24 | Transgenomic, Inc. | Apparatus and method for separating and purifying polynucleotides |
| US20050136458A1 (en) * | 1998-12-31 | 2005-06-23 | Oligos, Etc, Inc. | Method for nucleic acid preparation |
| US6586586B1 (en) * | 2000-01-31 | 2003-07-01 | Isis Pharmaceuticals, Inc. | Purification of oligonucleotides |
| EP1412749A4 (en) * | 2001-06-28 | 2006-12-13 | Ia Inc | OPTICAL FIBER SENSOR ARRAY |
| US20030153741A1 (en) * | 2002-02-08 | 2003-08-14 | Marek Kwiatkowski | Methods for separating oligonucleotides |
| US7345163B2 (en) * | 2002-08-28 | 2008-03-18 | Quiatech Ab | Process for separating and deprotecting oligonucleotides |
| US20060178507A1 (en) * | 2004-12-30 | 2006-08-10 | Berry & Associates, Inc. | Fluorous oligonucleotide reagents and affinity purification of oligonucleotides |
| WO2006132588A1 (en) * | 2005-06-10 | 2006-12-14 | Quiatech Ab | Method for the purification of synthetic oligonucleotides containing one or several labels |
| EP4368628A4 (en) * | 2021-07-05 | 2025-11-26 | Japan Science & Tech Agency | NUCLEOTIDE PURIFICATION PROCESS, NUCLEOTIDE PURIFICATION DEVICE, HYDROPHOBIC REAGENT AND HYDROPHOBIC SUBSTRATE |
| CN116102599B (zh) * | 2022-12-29 | 2024-08-09 | 苏州梓熙生物科技有限公司 | 寡核苷酸氨解方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU638599A1 (ru) * | 1977-07-11 | 1978-12-25 | Московский Ордена Ленина И Ордена Трудового Красного Знамени Государственный Университет Им. М.В.Ломоносова | Способ получени фракций нуклеиновых кислот |
| US4430496A (en) * | 1980-01-17 | 1984-02-07 | Varian Associates, Inc. | Strong anion exchange composition and methods |
| JPS5862199A (ja) * | 1981-10-09 | 1983-04-13 | Wakunaga Yakuhin Kk | 精製された５′−末端トリリン酸化オリゴヌクレオチドの製造法 |
| SU1129213A1 (ru) * | 1982-06-01 | 1984-12-15 | Предприятие П/Я Г-4740 | Способ выделени нуклеозид-5-монофосфорных кислот |
| EP0108387B1 (en) * | 1982-11-04 | 1990-05-16 | F. Hoffmann-La Roche Ag | Preparation of recombinant growth releasing factors |
| JPS59104399A (ja) * | 1982-12-03 | 1984-06-16 | Takeda Chem Ind Ltd | ヌクレオチドおよびヌクレオシドの相互分離方法 |
| JPS604174A (ja) * | 1983-06-22 | 1985-01-10 | Toyo Soda Mfg Co Ltd | 核酸塩基およびヌクレオシドとヌクレオチドの分離方法 |
| JPS6036493A (ja) * | 1983-08-08 | 1985-02-25 | Nippon Zeon Co Ltd | 保護された核酸関連物質の分離法 |
| GB8405763D0 (en) * | 1984-03-06 | 1984-04-11 | Shell Int Research | Dissolution of nucleotides and polynucleotides in non-aqueous solvents |
| DE3433649A1 (de) * | 1984-09-13 | 1986-03-20 | Gesellschaft für Biotechnologische Forschung mbH (GBF), 3300 Braunschweig | Verfahren zur aufreinigung synthetischer oligonucleotide |
| DE3678988D1 (de) * | 1985-03-28 | 1991-06-06 | Chiron Corp | Reinigung von synthetischen oligomeren. |
-
1984
- 1984-09-13 DE DE19843433649 patent/DE3433649A1/de not_active Withdrawn
-
1985
- 1985-08-20 EP EP85110454A patent/EP0174525B1/de not_active Expired - Lifetime
- 1985-08-20 AT AT85110454T patent/ATE55392T1/de not_active IP Right Cessation
- 1985-08-20 DE DE8585110454T patent/DE3579081D1/de not_active Expired - Lifetime
- 1985-08-27 US US06/770,295 patent/US4997927A/en not_active Expired - Lifetime
- 1985-09-12 DK DK198504156A patent/DK174507B1/da not_active IP Right Cessation
- 1985-09-12 CA CA000490568A patent/CA1288363C/en not_active Expired - Lifetime
- 1985-09-13 JP JP60201877A patent/JPS6172797A/ja active Granted
Non-Patent Citations (1)
| Title |
|---|
| BIOCHEMICAL & BIOPHYSICAL RESEARCH COMMUNICATIONS=1974 * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11127854A (ja) * | 1997-10-28 | 1999-05-18 | Hitachi Ltd | 核酸の回収方法及び装置 |
| JPH11266864A (ja) * | 1998-03-19 | 1999-10-05 | Hitachi Ltd | 核酸の精製方法および精製用装置 |
| JP2000166556A (ja) * | 1998-12-10 | 2000-06-20 | Hitachi Ltd | 核酸の回収方法及び装置 |
| JP2002191351A (ja) * | 2001-10-19 | 2002-07-09 | Hitachi Ltd | 核酸の精製用装置および核酸捕捉用チップ |
| JP2005538116A (ja) * | 2002-08-02 | 2005-12-15 | シクロプス ゲノム サイエンス リミテッド | 核酸の安定化 |
| JP2004298195A (ja) * | 2004-07-09 | 2004-10-28 | Hitachi Ltd | 核酸の回収方法 |
| JP2007330271A (ja) * | 2007-09-21 | 2007-12-27 | Hitachi Ltd | 核酸の回収方法 |
| JP2019518759A (ja) * | 2016-06-14 | 2019-07-04 | バイオジェン・エムエイ・インコーポレイテッドＢｉｏｇｅｎ ＭＡ Ｉｎｃ． | オリゴヌクレオチドの精製のための疎水性相互作用クロマトグラフィー |
Also Published As
| Publication number | Publication date |
|---|---|
| US4997927A (en) | 1991-03-05 |
| DK415685A (da) | 1986-03-14 |
| EP0174525A3 (en) | 1986-12-30 |
| JPH0556359B2 (en:Method) | 1993-08-19 |
| CA1288363C (en) | 1991-09-03 |
| EP0174525B1 (de) | 1990-08-08 |
| DK174507B1 (da) | 2003-05-05 |
| ATE55392T1 (de) | 1990-08-15 |
| DK415685D0 (da) | 1985-09-12 |
| DE3579081D1 (de) | 1990-09-13 |
| DE3433649A1 (de) | 1986-03-20 |
| EP0174525A2 (de) | 1986-03-19 |
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| DE69619825T2 (de) | Kombinatorische bibliotheken aus markierten biochemischen verbindungen und verfahren zu ihrer herstellung | |
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