JP2012513386A - 核酸の精製方法 - Google Patents
核酸の精製方法 Download PDFInfo
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- JP2012513386A JP2012513386A JP2011541520A JP2011541520A JP2012513386A JP 2012513386 A JP2012513386 A JP 2012513386A JP 2011541520 A JP2011541520 A JP 2011541520A JP 2011541520 A JP2011541520 A JP 2011541520A JP 2012513386 A JP2012513386 A JP 2012513386A
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- nucleic acid
- support
- binding
- propyl
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 85
- 238000001821 nucleic acid purification Methods 0.000 title abstract description 6
- 150000007523 nucleic acids Chemical class 0.000 claims abstract description 172
- 108020004707 nucleic acids Proteins 0.000 claims abstract description 163
- 102000039446 nucleic acids Human genes 0.000 claims abstract description 163
- 230000027455 binding Effects 0.000 claims abstract description 153
- 238000010828 elution Methods 0.000 claims abstract description 63
- 150000003839 salts Chemical class 0.000 claims abstract description 30
- 230000007935 neutral effect Effects 0.000 claims abstract description 14
- 239000003999 initiator Substances 0.000 claims description 68
- 229910052757 nitrogen Inorganic materials 0.000 claims description 66
- 239000003446 ligand Substances 0.000 claims description 61
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 60
- 239000000463 material Substances 0.000 claims description 55
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 43
- 229910000077 silane Inorganic materials 0.000 claims description 41
- 239000000178 monomer Substances 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 37
- -1 polyethylene Polymers 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 32
- 229920000642 polymer Polymers 0.000 claims description 31
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 29
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 28
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 14
- 239000012149 elution buffer Substances 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 13
- UNVFWCQQWZUPLB-UHFFFAOYSA-N 3-[dimethoxy(pentan-3-yloxy)silyl]propan-1-amine Chemical compound CCC(CC)O[Si](OC)(OC)CCCN UNVFWCQQWZUPLB-UHFFFAOYSA-N 0.000 claims description 12
- 230000004048 modification Effects 0.000 claims description 11
- 238000012986 modification Methods 0.000 claims description 11
- 150000004756 silanes Chemical class 0.000 claims description 11
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 9
- 239000012148 binding buffer Substances 0.000 claims description 9
- 239000011521 glass Substances 0.000 claims description 9
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 9
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000000524 functional group Chemical group 0.000 claims description 8
- 150000004820 halides Chemical class 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 238000007306 functionalization reaction Methods 0.000 claims description 7
- GXGGOCHUJJTJGF-UHFFFAOYSA-N 2-(chloromethyl)prop-2-enyl-trimethoxysilane Chemical group CO[Si](OC)(OC)CC(=C)CCl GXGGOCHUJJTJGF-UHFFFAOYSA-N 0.000 claims description 6
- OMNHRTSJVBKLEU-UHFFFAOYSA-N 2-bromo-6-[ethoxy(dimethyl)silyl]-2-methylhexan-3-one Chemical group CCO[Si](C)(C)CCCC(=O)C(C)(C)Br OMNHRTSJVBKLEU-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 5
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 5
- 239000001273 butane Substances 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
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- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 229920000058 polyacrylate Polymers 0.000 claims description 5
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 4
- 239000005046 Chlorosilane Substances 0.000 claims description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 4
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 claims description 4
- 235000011187 glycerol Nutrition 0.000 claims description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 4
- MVVMETRGWFSULN-UHFFFAOYSA-N n',n',2-trimethyl-n-propylprop-2-enehydrazide Chemical compound CCCN(N(C)C)C(=O)C(C)=C MVVMETRGWFSULN-UHFFFAOYSA-N 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- 150000003077 polyols Chemical group 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims description 4
- YXMISKNUHHOXFT-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) prop-2-enoate Chemical compound C=CC(=O)ON1C(=O)CCC1=O YXMISKNUHHOXFT-UHFFFAOYSA-N 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims description 3
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 claims description 3
- HQCSZRIVJVOYSU-UHFFFAOYSA-N 2-(ethoxymethyl)oxirane Chemical class CCOCC1CO1 HQCSZRIVJVOYSU-UHFFFAOYSA-N 0.000 claims description 3
- SVYHMICYJHWXIN-UHFFFAOYSA-N 2-[di(propan-2-yl)amino]ethyl 2-methylprop-2-enoate Chemical compound CC(C)N(C(C)C)CCOC(=O)C(C)=C SVYHMICYJHWXIN-UHFFFAOYSA-N 0.000 claims description 3
- UBKOBOIZDIWIFU-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOCC1CO1 UBKOBOIZDIWIFU-UHFFFAOYSA-N 0.000 claims description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- YSUJQSICLYYXGD-UHFFFAOYSA-N N-ethyl-2-methyl-N',N'-di(propan-2-yl)prop-2-enehydrazide Chemical compound C(C(=C)C)(=O)N(N(C(C)C)C(C)C)CC YSUJQSICLYYXGD-UHFFFAOYSA-N 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001720 carbohydrates Chemical class 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 150000002118 epoxides Chemical group 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- NCKDQUKVMYKEDN-UHFFFAOYSA-N n',n'-diethyl-2-methyl-n-propylprop-2-enehydrazide Chemical compound CCCN(N(CC)CC)C(=O)C(C)=C NCKDQUKVMYKEDN-UHFFFAOYSA-N 0.000 claims description 3
- HBVCJGDADPMZEC-UHFFFAOYSA-N n',n'-diethyl-n-propylprop-2-enehydrazide Chemical compound CCCN(N(CC)CC)C(=O)C=C HBVCJGDADPMZEC-UHFFFAOYSA-N 0.000 claims description 3
- JQQGOMZGMWOLIJ-UHFFFAOYSA-N n,n',n'-triethyl-2-methylprop-2-enehydrazide Chemical compound CCN(CC)N(CC)C(=O)C(C)=C JQQGOMZGMWOLIJ-UHFFFAOYSA-N 0.000 claims description 3
- GAYDVWRHTHHMGO-UHFFFAOYSA-N n,n',n'-triethylprop-2-enehydrazide Chemical compound CCN(CC)N(CC)C(=O)C=C GAYDVWRHTHHMGO-UHFFFAOYSA-N 0.000 claims description 3
- YHOSNAAUPKDRMI-UHFFFAOYSA-N n,n-di(propan-2-yl)prop-2-enamide Chemical compound CC(C)N(C(C)C)C(=O)C=C YHOSNAAUPKDRMI-UHFFFAOYSA-N 0.000 claims description 3
- GUAQVFRUPZBRJQ-UHFFFAOYSA-N n-(3-aminopropyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCCN GUAQVFRUPZBRJQ-UHFFFAOYSA-N 0.000 claims description 3
- QNCPCGJTMRRTOH-UHFFFAOYSA-N n-[1-(dimethylamino)propyl]prop-2-enamide Chemical compound CCC(N(C)C)NC(=O)C=C QNCPCGJTMRRTOH-UHFFFAOYSA-N 0.000 claims description 3
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 claims description 3
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Natural products CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 3
- 150000004072 triols Chemical group 0.000 claims description 3
- 229920000936 Agarose Polymers 0.000 claims description 2
- 229920002307 Dextran Polymers 0.000 claims description 2
- NNJFCQWJLJDOMN-UHFFFAOYSA-N N',N'-di(propan-2-yl)-N-propylprop-2-enehydrazide Chemical compound CCCN(N(C(C)C)C(C)C)C(=O)C=C NNJFCQWJLJDOMN-UHFFFAOYSA-N 0.000 claims description 2
- ZOQRSOLCFSVKHB-UHFFFAOYSA-N N-ethyl-N',N'-di(propan-2-yl)prop-2-enehydrazide Chemical compound C(C=C)(=O)N(N(C(C)C)C(C)C)CC ZOQRSOLCFSVKHB-UHFFFAOYSA-N 0.000 claims description 2
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- QIOYHIUHPGORLS-UHFFFAOYSA-N n,n-dimethyl-3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN(C)C QIOYHIUHPGORLS-UHFFFAOYSA-N 0.000 claims description 2
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- RSMSNGDEGGHXOY-UHFFFAOYSA-N n-ethyl-n',n',2-trimethylprop-2-enehydrazide Chemical compound CCN(N(C)C)C(=O)C(C)=C RSMSNGDEGGHXOY-UHFFFAOYSA-N 0.000 claims description 2
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
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- KCIPGHYGHSNNLE-UHFFFAOYSA-N C(C)C=C(C(=O)NN(C)C)C Chemical compound C(C)C=C(C(=O)NN(C)C)C KCIPGHYGHSNNLE-UHFFFAOYSA-N 0.000 claims 1
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- 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
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| JP5899731B2 (ja) | 2011-09-13 | 2016-04-06 | ソニー株式会社 | 核酸精製方法、核酸抽出方法、及び核酸精製用キット |
| EP2760999A1 (en) | 2011-09-26 | 2014-08-06 | Qiagen GmbH | Methods for separating nucleic acids by size |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2016135784A (ja) | 2016-07-28 |
| CN102264902B (zh) | 2018-06-01 |
| AU2009332900B2 (en) | 2014-05-29 |
| AU2009332900A1 (en) | 2010-07-01 |
| US9102935B2 (en) | 2015-08-11 |
| EP2382315A1 (de) | 2011-11-02 |
| DE102008063001A1 (de) | 2010-06-24 |
| CN102264902A (zh) | 2011-11-30 |
| EP2382315B1 (de) | 2015-09-23 |
| JP6072945B2 (ja) | 2017-02-01 |
| US20110319506A1 (en) | 2011-12-29 |
| WO2010072834A1 (de) | 2010-07-01 |
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