KR20050088164A - 핵산 단리방법 - Google Patents
핵산 단리방법 Download PDFInfo
- Publication number
- KR20050088164A KR20050088164A KR1020057014820A KR20057014820A KR20050088164A KR 20050088164 A KR20050088164 A KR 20050088164A KR 1020057014820 A KR1020057014820 A KR 1020057014820A KR 20057014820 A KR20057014820 A KR 20057014820A KR 20050088164 A KR20050088164 A KR 20050088164A
- Authority
- KR
- South Korea
- Prior art keywords
- solid phase
- nucleic acid
- blood
- biological
- dna
- 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.)
- Ceased
Links
- 108020004707 nucleic acids Proteins 0.000 title claims abstract description 35
- 102000039446 nucleic acids Human genes 0.000 title claims abstract description 35
- 150000007523 nucleic acids Chemical class 0.000 title claims abstract description 35
- 238000002955 isolation Methods 0.000 title claims description 5
- 238000000034 method Methods 0.000 claims abstract description 53
- 239000007790 solid phase Substances 0.000 claims abstract description 47
- 210000004369 blood Anatomy 0.000 claims abstract description 38
- 239000008280 blood Substances 0.000 claims abstract description 38
- 239000011324 bead Substances 0.000 claims abstract description 20
- 239000011230 binding agent Substances 0.000 claims abstract description 6
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000004033 plastic Substances 0.000 claims description 16
- 239000000523 sample Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 13
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 10
- 239000012472 biological sample Substances 0.000 claims description 9
- 238000000605 extraction Methods 0.000 claims description 7
- 229920002704 polyhistidine Polymers 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 125000000524 functional group Chemical group 0.000 claims description 6
- -1 polypropylene Polymers 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- RJURFGZVJUQBHK-UHFFFAOYSA-N actinomycin D Natural products CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)NC4C(=O)NC(C(N5CCCC5C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-UHFFFAOYSA-N 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 239000003599 detergent Substances 0.000 claims description 4
- 238000010790 dilution Methods 0.000 claims description 4
- 239000012895 dilution Substances 0.000 claims description 4
- 238000010828 elution Methods 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 4
- 238000003780 insertion Methods 0.000 claims description 4
- 230000037431 insertion Effects 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 108091005804 Peptidases Proteins 0.000 claims description 3
- 239000004365 Protease Substances 0.000 claims description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 230000003196 chaotropic effect Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 108010092160 Dactinomycin Proteins 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- RJURFGZVJUQBHK-IIXSONLDSA-N actinomycin D Chemical group C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-IIXSONLDSA-N 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 239000007853 buffer solution Substances 0.000 claims description 2
- 229910010293 ceramic material Inorganic materials 0.000 claims description 2
- 125000003636 chemical group Chemical group 0.000 claims description 2
- 229960000640 dactinomycin Drugs 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 claims description 2
- 229960005542 ethidium bromide Drugs 0.000 claims description 2
- 238000012252 genetic analysis Methods 0.000 claims description 2
- 238000010353 genetic engineering Methods 0.000 claims description 2
- 150000004676 glycans Chemical class 0.000 claims description 2
- 230000005660 hydrophilic surface Effects 0.000 claims description 2
- 230000005661 hydrophobic surface Effects 0.000 claims description 2
- 230000003993 interaction Effects 0.000 claims description 2
- 239000003456 ion exchange resin Substances 0.000 claims description 2
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 2
- 239000003446 ligand Substances 0.000 claims description 2
- 238000010137 moulding (plastic) Methods 0.000 claims description 2
- 239000002773 nucleotide Substances 0.000 claims description 2
- 125000003729 nucleotide group Chemical group 0.000 claims description 2
- 230000003204 osmotic effect Effects 0.000 claims description 2
- 239000007800 oxidant agent Substances 0.000 claims description 2
- 229920000768 polyamine Polymers 0.000 claims description 2
- 229920001282 polysaccharide Polymers 0.000 claims description 2
- 239000005017 polysaccharide Substances 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- 239000012266 salt solution Substances 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 239000011343 solid material Substances 0.000 claims 8
- 239000012620 biological material Substances 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims 1
- 239000005289 controlled pore glass Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 239000002907 paramagnetic material Substances 0.000 claims 1
- 230000008961 swelling Effects 0.000 claims 1
- 239000011521 glass Substances 0.000 abstract description 8
- 230000002934 lysing effect Effects 0.000 abstract description 3
- 210000000601 blood cell Anatomy 0.000 abstract 1
- 239000012530 fluid Substances 0.000 abstract 1
- 108020004414 DNA Proteins 0.000 description 17
- 229920001213 Polysorbate 20 Polymers 0.000 description 7
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 7
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- 239000000872 buffer Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 3
- 238000007400 DNA extraction Methods 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000003491 array Methods 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 230000005291 magnetic effect Effects 0.000 description 2
- 230000005298 paramagnetic effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920000936 Agarose Polymers 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 108020005120 Plant DNA Proteins 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000012412 chemical coupling Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000004413 injection moulding compound Substances 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 238000005070 sampling Methods 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
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
- C12N15/1006—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
- C12N15/1006—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers
- C12N15/101—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers by chromatography, e.g. electrophoresis, ion-exchange, reverse phase
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Microbiology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9725839.6 | 1997-12-06 | ||
| GBGB9725839.6A GB9725839D0 (en) | 1997-12-06 | 1997-12-06 | Isolation of nucleic acids |
| GB9815541.9 | 1998-07-17 | ||
| GBGB9815541.9A GB9815541D0 (en) | 1998-07-17 | 1998-07-17 | Isolation of nucleic acids |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020007006123A Division KR20010032806A (ko) | 1997-12-06 | 1998-12-04 | 핵산 분리방법 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20050088164A true KR20050088164A (ko) | 2005-09-01 |
Family
ID=26312726
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020057014820A Ceased KR20050088164A (ko) | 1997-12-06 | 1998-12-04 | 핵산 단리방법 |
| KR1020007006123A Ceased KR20010032806A (ko) | 1997-12-06 | 1998-12-04 | 핵산 분리방법 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020007006123A Ceased KR20010032806A (ko) | 1997-12-06 | 1998-12-04 | 핵산 분리방법 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20030130499A1 (enExample) |
| EP (2) | EP1036082B1 (enExample) |
| JP (2) | JP2004501054A (enExample) |
| KR (2) | KR20050088164A (enExample) |
| CN (1) | CN1230440C (enExample) |
| AT (2) | ATE218140T1 (enExample) |
| AU (1) | AU755342B2 (enExample) |
| BR (1) | BR9815569A (enExample) |
| CA (1) | CA2318306A1 (enExample) |
| DE (2) | DE69839133T2 (enExample) |
| DK (1) | DK1036082T3 (enExample) |
| ES (2) | ES2301581T3 (enExample) |
| NO (1) | NO315323B1 (enExample) |
| PT (1) | PT1036082E (enExample) |
| WO (1) | WO1999029703A2 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101308685B1 (ko) * | 2005-10-31 | 2013-09-13 | 엑시스-시일드 에이에스에이 | 막 분석 방법 |
| WO2014035090A1 (ko) | 2012-08-28 | 2014-03-06 | 주식회사 바이오큐브시스템 | 생물학적 시료로부터 핵산 증폭 반응용 생물학적 분자를 신속하게 분리하기 위한 다공성 고체상 및 이의 용도 |
Families Citing this family (114)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9425138D0 (en) * | 1994-12-12 | 1995-02-08 | Dynal As | Isolation of nucleic acid |
| US6914137B2 (en) * | 1997-12-06 | 2005-07-05 | Dna Research Innovations Limited | Isolation of nucleic acids |
| JP2002541839A (ja) * | 1999-04-21 | 2002-12-10 | アノビス， インコーポレイテッド | 植物についての磁気ｄｎａ抽出キット |
| US6383783B1 (en) * | 1999-09-21 | 2002-05-07 | 3M Innovative Properties Company | Nucleic acid isolation by adhering to hydrophobic solid phase and removing with nonionic surfactant |
| SE9904539D0 (sv) * | 1999-12-10 | 1999-12-10 | Alphahelix Ab | Method and device for the handling of samples and reagents |
| JP2001221721A (ja) * | 2000-02-09 | 2001-08-17 | Sapporo Imuno Diagnostic Laboratory:Kk | 乾燥濾紙便による遺伝子診断 |
| DE10006590B4 (de) * | 2000-02-11 | 2007-10-18 | Qiagen North American Holdings, Inc. | Verwendung funktionalisierter Membranen bzw. Matrizes zur Aufreinigung von Nukleinsäuren sowie entsprechende Verfahren |
| CA2433746A1 (en) * | 2001-01-09 | 2002-07-18 | Whitehead Institute For Biomedical Research | Methods and reagents for the isolation of nucleic acids |
| US7829025B2 (en) | 2001-03-28 | 2010-11-09 | Venture Lending & Leasing Iv, Inc. | Systems and methods for thermal actuation of microfluidic devices |
| US8895311B1 (en) | 2001-03-28 | 2014-11-25 | Handylab, Inc. | Methods and systems for control of general purpose microfluidic devices |
| CA2473376A1 (en) | 2002-01-16 | 2003-07-31 | Dynal Biotech Asa | Method for isolating nucleic acids and protein from a single sample |
| GB0212826D0 (en) | 2002-05-31 | 2002-07-10 | Dna Res Innovations Ltd | Materials and methods relating to polyions and substance delivery |
| GB0212825D0 (en) * | 2002-05-31 | 2002-07-10 | Dna Res Innovations Ltd | Methods compositions and kits for cell separation |
| GB0229287D0 (en) * | 2002-12-16 | 2003-01-22 | Dna Res Innovations Ltd | Polyfunctional reagents |
| US7601491B2 (en) | 2003-02-06 | 2009-10-13 | Becton, Dickinson And Company | Pretreatment method for extraction of nucleic acid from biological samples and kits therefor |
| US20040197780A1 (en) * | 2003-04-02 | 2004-10-07 | Agencourt Bioscience Corporation | Method for isolating nucleic acids |
| CN100395257C (zh) * | 2003-05-08 | 2008-06-18 | 慈溪市中鼎生物技术有限公司 | 钾离子酸性水溶液和利用这种溶液的dna提取方法和试剂盒 |
| WO2005011867A2 (en) | 2003-07-31 | 2005-02-10 | Handylab, Inc. | Processing particle-containing samples |
| US8852862B2 (en) | 2004-05-03 | 2014-10-07 | Handylab, Inc. | Method for processing polynucleotide-containing samples |
| CA2565572C (en) * | 2004-05-03 | 2018-03-06 | Handylab, Inc. | A microfluidic device and methods for processing polynucleotide-containing samples |
| US20060010513A1 (en) * | 2004-05-11 | 2006-01-12 | Melville Mark W | Oligonucleotide arrays to monitor gene expression and methods for making and using same |
| US20060024712A1 (en) * | 2004-06-25 | 2006-02-02 | Invitrogen Corporation | Separation of nucleic acid |
| EP1778877B1 (en) | 2004-07-28 | 2009-10-21 | Canon U.S. Life Sciences, Inc. | Methods for monitoring genomic dna of organisms |
| EP1776458A2 (en) * | 2004-07-30 | 2007-04-25 | Agencourt Bioscience Corporation | Methods of isolating nucleic acids using multifunctional group-coated solid phase carriers |
| WO2006017428A2 (en) * | 2004-08-03 | 2006-02-16 | Becton, Dickinson And Company | Use of magnetic material to direct isolation of compounds and fractionation of multipart samples |
| KR100647306B1 (ko) * | 2004-12-23 | 2006-11-23 | 삼성전자주식회사 | 아미노기와 카르복실기를 포함하고 제1 ｐＨ에서 양전하를띠는 물질을 이용하여 핵산을 분리하는 방법 |
| US7964380B2 (en) | 2005-01-21 | 2011-06-21 | Argylia Technologies | Nanoparticles for manipulation of biopolymers and methods of thereof |
| US20060166223A1 (en) * | 2005-01-26 | 2006-07-27 | Reed Michael W | DNA purification and analysis on nanoengineered surfaces |
| KR100647315B1 (ko) * | 2005-02-02 | 2006-11-23 | 삼성전자주식회사 | 실란화된 고상 물질을 이용한 핵산의 분리 및 증폭 방법 |
| WO2006089192A2 (en) * | 2005-02-18 | 2006-08-24 | Canon U.S. Life Sciences, Inc. | Devices and methods for identifying genomic dna of organisms |
| US20060234251A1 (en) * | 2005-04-19 | 2006-10-19 | Lumigen, Inc. | Methods of enhancing isolation of RNA from biological samples |
| KR100668337B1 (ko) * | 2005-05-21 | 2007-01-12 | 삼성전자주식회사 | 단백질에 비하여 핵산에 대한 결합력이 선택적으로 높은ｐＨ 의존성 이온 교환물질, 그가 고정화되어 있는 고체기판, 및 상기 물질 및 고체 기판을 이용하여 핵산을분리하는 방법 |
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| KR101308685B1 (ko) * | 2005-10-31 | 2013-09-13 | 엑시스-시일드 에이에스에이 | 막 분석 방법 |
| WO2014035090A1 (ko) | 2012-08-28 | 2014-03-06 | 주식회사 바이오큐브시스템 | 생물학적 시료로부터 핵산 증폭 반응용 생물학적 분자를 신속하게 분리하기 위한 다공성 고체상 및 이의 용도 |
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| AU755342B2 (en) | 2002-12-12 |
| EP1234832B1 (en) | 2008-02-13 |
| CN1230440C (zh) | 2005-12-07 |
| AU1344799A (en) | 1999-06-28 |
| DE69839133D1 (de) | 2008-03-27 |
| ES2177093T3 (es) | 2002-12-01 |
| EP1036082A2 (en) | 2000-09-20 |
| DE69805649D1 (de) | 2002-07-04 |
| PT1036082E (pt) | 2002-10-31 |
| NO20002540L (no) | 2000-07-07 |
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