FI105555B - Infrapuna-väriaineella merkityt nukleotidit ja niiden käyttö nukleiinihappojen osoittamiseksi - Google Patents
Infrapuna-väriaineella merkityt nukleotidit ja niiden käyttö nukleiinihappojen osoittamiseksi Download PDFInfo
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- FI105555B FI105555B FI951630A FI951630A FI105555B FI 105555 B FI105555 B FI 105555B FI 951630 A FI951630 A FI 951630A FI 951630 A FI951630 A FI 951630A FI 105555 B FI105555 B FI 105555B
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- 150000002730 mercury Chemical class 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000004712 monophosphates Chemical class 0.000 description 1
- 238000003541 multi-stage reaction Methods 0.000 description 1
- 239000006225 natural substrate Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000009871 nonspecific binding Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 229910000064 phosphane Inorganic materials 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 239000002212 purine nucleoside Substances 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000002901 radioactive waste Substances 0.000 description 1
- 239000011535 reaction buffer Substances 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004366 reverse phase liquid chromatography 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
- 239000002336 ribonucleotide Substances 0.000 description 1
- 125000002652 ribonucleotide group Chemical group 0.000 description 1
- 229920002477 rna polymer Polymers 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- WGTODYJZXSJIAG-UHFFFAOYSA-N tetramethylrhodamine chloride Chemical compound [Cl-].C=12C=CC(N(C)C)=CC2=[O+]C2=CC(N(C)C)=CC=C2C=1C1=CC=CC=C1C(O)=O WGTODYJZXSJIAG-UHFFFAOYSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 125000002264 triphosphate group Chemical class [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- DRTQHJPVMGBUCF-UHFFFAOYSA-N uracil arabinoside Natural products OC1C(O)C(CO)OC1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-UHFFFAOYSA-N 0.000 description 1
- 229940045145 uridine Drugs 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
- C07F9/5728—Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Saccharide Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4326466 | 1993-08-06 | ||
DE4326466A DE4326466A1 (de) | 1993-08-06 | 1993-08-06 | Infrarot-Farbstoff-markierte Nucleotide und ihre Verwendung in der Nucleinsäure-Detektion |
PCT/EP1994/002541 WO1995004747A1 (de) | 1993-08-06 | 1994-07-30 | Infrarot-farbstoff-markierte nucleotide und ihre verwendung in der nucleinsäure-detektion |
EP9402541 | 1994-07-30 |
Publications (3)
Publication Number | Publication Date |
---|---|
FI951630A FI951630A (fi) | 1995-04-05 |
FI951630A0 FI951630A0 (fi) | 1995-04-05 |
FI105555B true FI105555B (fi) | 2000-09-15 |
Family
ID=6494618
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI951630A FI105555B (fi) | 1993-08-06 | 1995-04-05 | Infrapuna-väriaineella merkityt nukleotidit ja niiden käyttö nukleiinihappojen osoittamiseksi |
Country Status (14)
Country | Link |
---|---|
US (1) | US6573374B1 (ja) |
EP (1) | EP0663922B1 (ja) |
JP (2) | JP2966524B2 (ja) |
KR (2) | KR0156095B1 (ja) |
AT (1) | ATE186304T1 (ja) |
AU (2) | AU671928B2 (ja) |
CA (1) | CA2145405C (ja) |
DE (2) | DE4326466A1 (ja) |
DK (1) | DK0663922T3 (ja) |
ES (1) | ES2140551T3 (ja) |
FI (1) | FI105555B (ja) |
NO (1) | NO303543B1 (ja) |
NZ (1) | NZ271092A (ja) |
WO (1) | WO1995004747A1 (ja) |
Families Citing this family (43)
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US5571388A (en) * | 1984-03-29 | 1996-11-05 | Li-Cor, Inc. | Sequencing near infrared and infrared fluorescense labeled DNA for detecting using laser diodes and suitable labels thereof |
US4729947A (en) * | 1984-03-29 | 1988-03-08 | The Board Of Regents Of The University Of Nebraska | DNA sequencing |
US6207421B1 (en) | 1984-03-29 | 2001-03-27 | Li-Cor, Inc. | DNA sequencing and DNA terminators |
US6004446A (en) * | 1984-03-29 | 1999-12-21 | Li-Cor, Inc. | DNA Sequencing |
US5360523A (en) * | 1984-03-29 | 1994-11-01 | Li-Cor, Inc. | DNA sequencing |
US6956032B1 (en) | 1986-04-18 | 2005-10-18 | Carnegie Mellon University | Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods |
US6048982A (en) * | 1986-04-18 | 2000-04-11 | Carnegie Mellon University | Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods |
US6225050B1 (en) | 1986-04-18 | 2001-05-01 | Carnegie Mellon University | Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods |
US5808044A (en) * | 1993-01-22 | 1998-09-15 | Pharmacia Biotech Inc. | Indocarbocyanine and benzindocarbocyanine phosphoramidites |
US6593148B1 (en) | 1994-03-01 | 2003-07-15 | Li-Cor, Inc. | Cyanine dye compounds and labeling methods |
US6150510A (en) | 1995-11-06 | 2000-11-21 | Aventis Pharma Deutschland Gmbh | Modified oligonucleotides, their preparation and their use |
DE4438918A1 (de) * | 1994-11-04 | 1996-05-09 | Hoechst Ag | Modifizierte Oligonukleotide, deren Herstellung sowie deren Verwendung |
JP4981197B2 (ja) * | 1996-10-08 | 2012-07-18 | クレアテク バイオテクノロジー ベー.ファー. | ヌクレオチドを標識付けする方法、標識ヌクレオチド及び有用な中間体 |
US6027709A (en) * | 1997-01-10 | 2000-02-22 | Li-Cor Inc. | Fluorescent cyanine dyes |
US5986086A (en) * | 1997-06-20 | 1999-11-16 | Amersham Pharmacia Biotech Inc. | Non-sulfonated cyanine dyes for labeling nucleosides and nucleotides |
US7875440B2 (en) | 1998-05-01 | 2011-01-25 | Arizona Board Of Regents | Method of determining the nucleotide sequence of oligonucleotides and DNA molecules |
US6780591B2 (en) | 1998-05-01 | 2004-08-24 | Arizona Board Of Regents | Method of determining the nucleotide sequence of oligonucleotides and DNA molecules |
EP1163372A4 (en) * | 1999-03-24 | 2002-10-02 | Princeton Separations | CHEMICALLY REACTIVE CYANINE DYES AND DERIVATIVES IN A LEVEL |
US6818395B1 (en) | 1999-06-28 | 2004-11-16 | California Institute Of Technology | Methods and apparatus for analyzing polynucleotide sequences |
JP4989013B2 (ja) * | 2000-09-19 | 2012-08-01 | リ−コール インコーポレーティッド | シアニン色素 |
US7597878B2 (en) | 2000-09-19 | 2009-10-06 | Li-Cor, Inc. | Optical fluorescent imaging |
EP1317464B1 (en) * | 2000-10-11 | 2009-05-13 | Applera Corporation | Fluorescent nucleobase conjugates having anionic linkers |
US6331632B1 (en) * | 2000-11-09 | 2001-12-18 | Beckman Coulter, Inc. | Cyanine dye phosphoramidites |
EP1221465A1 (en) * | 2001-01-03 | 2002-07-10 | Innosense S.r.l. | Symmetric, monofunctionalised polymethine dyes labelling reagents |
EP1368497A4 (en) * | 2001-03-12 | 2007-08-15 | California Inst Of Techn | METHOD AND DEVICE FOR ANALYZING POLYNUCLEOTIDE SEQUENCES BY ASYNCHRONOUS BASE EXTENSION |
ATE508188T1 (de) | 2002-02-01 | 2011-05-15 | Life Technologies Corp | Oligonukleotid-zusammensetzungen mit verbesserter wirksamkeit |
US20060009409A1 (en) | 2002-02-01 | 2006-01-12 | Woolf Tod M | Double-stranded oligonucleotides |
WO2003064621A2 (en) * | 2002-02-01 | 2003-08-07 | Ambion, Inc. | HIGH POTENCY siRNAS FOR REDUCING THE EXPRESSION OF TARGET GENES |
AU2004247729A1 (en) * | 2003-06-12 | 2004-12-23 | Applera Corporation | Combinatorial nucleobase oligomers comprising universal base analogues and methods for making and using same |
US7169560B2 (en) | 2003-11-12 | 2007-01-30 | Helicos Biosciences Corporation | Short cycle methods for sequencing polynucleotides |
EP1716254B1 (en) | 2004-02-19 | 2010-04-07 | Helicos Biosciences Corporation | Methods for analyzing polynucleotide sequences |
US7312326B2 (en) | 2004-04-09 | 2007-12-25 | Beckman Coulter, Inc. | Fluorescent labeled nucleotide derivatives |
US7910753B2 (en) | 2004-09-10 | 2011-03-22 | Anaspec Incorporated | Cyanine dyes and their applications as luminescence quenching compounds |
WO2006035207A2 (en) * | 2004-09-30 | 2006-04-06 | Ge Healthcare Uk Limited | Fluorescent nucleotide analogues |
US8227621B2 (en) | 2005-06-30 | 2012-07-24 | Li-Cor, Inc. | Cyanine dyes and methods of use |
US7666593B2 (en) | 2005-08-26 | 2010-02-23 | Helicos Biosciences Corporation | Single molecule sequencing of captured nucleic acids |
AR059193A1 (es) | 2006-01-31 | 2008-03-12 | Bayer Schering Pharma Ag | Modulacion de la actividad de mdl-1 para el tratamiento de enfermedades inflamatorias |
EP2005970A1 (de) | 2007-06-22 | 2008-12-24 | Berlin Science Partners GmbH i.V. | Bildgebende Diagnostik durch Kombination von Kontrastmitteln |
WO2011027218A1 (en) | 2009-09-04 | 2011-03-10 | Progenika Biopharma, S.A. | High throughput detection of genomic copy number variations |
WO2011027219A1 (en) | 2009-09-04 | 2011-03-10 | Progenika Biopharma, S.A. | High throughput detection of small genomic deletions and insertions |
US10017551B2 (en) | 2013-03-15 | 2018-07-10 | The Regents Of The University Of California | Peptides having reduced toxicity that stimulate cholesterol efflux |
KR20210132104A (ko) | 2019-02-19 | 2021-11-03 | 울티마 제노믹스, 인크. | 광학 검출 및 시퀀싱을 위한 링커 및 방법 |
US11807851B1 (en) | 2020-02-18 | 2023-11-07 | Ultima Genomics, Inc. | Modified polynucleotides and uses thereof |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4828979A (en) * | 1984-11-08 | 1989-05-09 | Life Technologies, Inc. | Nucleotide analogs for nucleic acid labeling and detection |
US5151507A (en) | 1986-07-02 | 1992-09-29 | E. I. Du Pont De Nemours And Company | Alkynylamino-nucleotides |
US5047519A (en) * | 1986-07-02 | 1991-09-10 | E. I. Du Pont De Nemours And Company | Alkynylamino-nucleotides |
US4997928A (en) * | 1988-09-15 | 1991-03-05 | E. I. Du Pont De Nemours And Company | Fluorescent reagents for the preparation of 5'-tagged oligonucleotides |
IL91673A0 (en) * | 1988-09-20 | 1990-04-29 | Us Health | Method for tagging an oligodeoxynucleotide |
DE69216498T2 (de) * | 1991-08-13 | 1997-04-30 | Bayer Ag | Fluoreszierendes Etikett |
-
1993
- 1993-08-06 DE DE4326466A patent/DE4326466A1/de not_active Withdrawn
-
1994
- 1994-07-30 JP JP7506207A patent/JP2966524B2/ja not_active Expired - Lifetime
- 1994-07-30 US US08/411,761 patent/US6573374B1/en not_active Expired - Lifetime
- 1994-07-30 ES ES94924305T patent/ES2140551T3/es not_active Expired - Lifetime
- 1994-07-30 NZ NZ271092A patent/NZ271092A/en not_active IP Right Cessation
- 1994-07-30 DK DK94924305T patent/DK0663922T3/da active
- 1994-07-30 AU AU74611/94A patent/AU671928B2/en not_active Expired
- 1994-07-30 WO PCT/EP1994/002541 patent/WO1995004747A1/de active IP Right Grant
- 1994-07-30 AT AT94924305T patent/ATE186304T1/de not_active IP Right Cessation
- 1994-07-30 CA CA002145405A patent/CA2145405C/en not_active Expired - Lifetime
- 1994-07-30 KR KR1019980702884A patent/KR0156095B1/ko not_active IP Right Cessation
- 1994-07-30 DE DE59408887T patent/DE59408887D1/de not_active Expired - Lifetime
- 1994-07-30 KR KR1019950701315A patent/KR0156042B1/ko not_active IP Right Cessation
- 1994-07-30 EP EP94924305A patent/EP0663922B1/de not_active Expired - Lifetime
-
1995
- 1995-04-05 FI FI951630A patent/FI105555B/fi not_active IP Right Cessation
- 1995-04-05 NO NO951319A patent/NO303543B1/no not_active IP Right Cessation
-
1996
- 1996-07-10 AU AU59424/96A patent/AU682290B2/en not_active Expired
-
1999
- 1999-01-21 JP JP01297599A patent/JP3266865B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DK0663922T3 (da) | 2000-04-10 |
FI951630A (fi) | 1995-04-05 |
NZ271092A (en) | 1996-11-26 |
ATE186304T1 (de) | 1999-11-15 |
KR0156042B1 (ko) | 1998-10-15 |
JP2966524B2 (ja) | 1999-10-25 |
KR0156095B1 (ko) | 1998-10-15 |
ES2140551T3 (es) | 2000-03-01 |
WO1995004747A1 (de) | 1995-02-16 |
AU7461194A (en) | 1995-02-28 |
NO303543B1 (no) | 1998-07-27 |
JP3266865B2 (ja) | 2002-03-18 |
CA2145405A1 (en) | 1995-02-16 |
FI951630A0 (fi) | 1995-04-05 |
AU5942496A (en) | 1996-09-19 |
JPH07507576A (ja) | 1995-08-24 |
EP0663922B1 (de) | 1999-11-03 |
AU671928B2 (en) | 1996-09-12 |
CA2145405C (en) | 2002-09-17 |
NO951319D0 (no) | 1995-04-05 |
AU682290B2 (en) | 1997-09-25 |
US6573374B1 (en) | 2003-06-03 |
KR950703571A (ko) | 1995-09-20 |
NO951319L (no) | 1995-04-05 |
JPH11286498A (ja) | 1999-10-19 |
EP0663922A1 (de) | 1995-07-26 |
DE59408887D1 (de) | 1999-12-09 |
DE4326466A1 (de) | 1995-02-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
HC | Name/ company changed in application |
Owner name: ROCHE DIAGNOSTICS GMBH |
|
MA | Patent expired |