JP4287284B2 - プラスチック製カセット中の欠陥のないポリアクリルアミド電気泳動ゲルの作製 - Google Patents
プラスチック製カセット中の欠陥のないポリアクリルアミド電気泳動ゲルの作製 Download PDFInfo
- Publication number
- JP4287284B2 JP4287284B2 JP2003571320A JP2003571320A JP4287284B2 JP 4287284 B2 JP4287284 B2 JP 4287284B2 JP 2003571320 A JP2003571320 A JP 2003571320A JP 2003571320 A JP2003571320 A JP 2003571320A JP 4287284 B2 JP4287284 B2 JP 4287284B2
- Authority
- JP
- Japan
- Prior art keywords
- gel
- sodium
- oxygen scavenger
- plastic
- enclosed
- 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.)
- Expired - Fee Related
Links
- 229920003023 plastic Polymers 0.000 title claims description 31
- 239000004033 plastic Substances 0.000 title claims description 31
- 229920002401 polyacrylamide Polymers 0.000 title claims description 28
- 238000001962 electrophoresis Methods 0.000 title claims description 24
- 239000000499 gel Substances 0.000 title description 50
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 52
- 235000010265 sodium sulphite Nutrition 0.000 claims description 26
- 229940123973 Oxygen scavenger Drugs 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 18
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims description 17
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 14
- 239000000178 monomer Substances 0.000 claims description 13
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 10
- 150000003254 radicals Chemical class 0.000 claims description 10
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 8
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 7
- -1 polyethylene terephthalate Polymers 0.000 claims description 7
- 229940083542 sodium Drugs 0.000 claims description 7
- 235000015424 sodium Nutrition 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical compound C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 claims description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 6
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 6
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 6
- 239000003431 cross linking reagent Substances 0.000 claims description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims description 4
- 235000010350 erythorbic acid Nutrition 0.000 claims description 4
- 239000004318 erythorbic acid Substances 0.000 claims description 4
- 229940026239 isoascorbic acid Drugs 0.000 claims description 4
- ZYZYQCACSQDPSB-UHFFFAOYSA-N 12,15-dioxatricyclo[8.6.0.02,7]hexadeca-1(10),2,4,6,8-pentaene-11,16-dione Chemical compound O=C1OCCOC(=O)C2=C1C=CC1=CC=CC=C21 ZYZYQCACSQDPSB-UHFFFAOYSA-N 0.000 claims description 3
- 229920001174 Diethylhydroxylamine Polymers 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 235000010323 ascorbic acid Nutrition 0.000 claims description 3
- 229960005070 ascorbic acid Drugs 0.000 claims description 3
- 239000011668 ascorbic acid Substances 0.000 claims description 3
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 claims description 3
- AGGFJZYMAXECOR-UHFFFAOYSA-N hexane-3,3-diol Chemical compound CCCC(O)(O)CC AGGFJZYMAXECOR-UHFFFAOYSA-N 0.000 claims description 3
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 claims description 3
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 235000010352 sodium erythorbate Nutrition 0.000 claims description 2
- 239000004320 sodium erythorbate Substances 0.000 claims description 2
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 6
- 230000000379 polymerizing effect Effects 0.000 claims 2
- 150000003926 acrylamides Chemical class 0.000 claims 1
- 238000005266 casting Methods 0.000 claims 1
- 230000005611 electricity Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 25
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 14
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 7
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 7
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 6
- 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 5
- 239000011148 porous material Substances 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 238000007348 radical reaction Methods 0.000 description 3
- 229920001824 Barex® Polymers 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000006166 lysate Substances 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
- 229920000638 styrene acrylonitrile Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UCLPNTKRPMTACI-UHFFFAOYSA-N 2-chloro-n-[2-(5-methoxy-1h-indol-3-yl)ethyl]acetamide Chemical compound COC1=CC=C2NC=C(CCNC(=O)CCl)C2=C1 UCLPNTKRPMTACI-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- 102000003846 Carbonic anhydrases Human genes 0.000 description 1
- 108090000209 Carbonic anhydrases Proteins 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 102000003505 Myosin Human genes 0.000 description 1
- 108060008487 Myosin Proteins 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- 108010058846 Ovalbumin Proteins 0.000 description 1
- 108010065081 Phosphorylase b Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 229920006383 Tyril Polymers 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 102000005936 beta-Galactosidase Human genes 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000001502 gel electrophoresis Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229940092253 ovalbumin Drugs 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
- G01N27/44747—Composition of gel or of carrier mixture
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/56—Acrylamide; Methacrylamide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/916—Hydrogel compositions
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/934—Electrodeposit, e.g. electrophoretic, xerographic
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Analytical Chemistry (AREA)
- Immunology (AREA)
- Polymers & Plastics (AREA)
- Electrochemistry (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Pathology (AREA)
- Dispersion Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Medicinal Preparation (AREA)
- Polymerisation Methods In General (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/087,140 US6846881B2 (en) | 2002-02-27 | 2002-02-27 | Preparation of defect-free polyacrylamide electrophoresis gels in plastic cassettes |
| PCT/US2003/006207 WO2003072616A1 (en) | 2002-02-27 | 2003-02-26 | Preparation of defect-free polyacrylamide electrophoresis gels in plastic cassettes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005519145A JP2005519145A (ja) | 2005-06-30 |
| JP2005519145A5 JP2005519145A5 (enExample) | 2006-06-22 |
| JP4287284B2 true JP4287284B2 (ja) | 2009-07-01 |
Family
ID=27753895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003571320A Expired - Fee Related JP4287284B2 (ja) | 2002-02-27 | 2003-02-26 | プラスチック製カセット中の欠陥のないポリアクリルアミド電気泳動ゲルの作製 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US6846881B2 (enExample) |
| EP (1) | EP1478670B1 (enExample) |
| JP (1) | JP4287284B2 (enExample) |
| AU (1) | AU2003212467C1 (enExample) |
| CA (1) | CA2476768C (enExample) |
| DE (1) | DE60322027D1 (enExample) |
| WO (1) | WO2003072616A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6846881B2 (en) * | 2002-02-27 | 2005-01-25 | Bio-Rad Laboratories, Inc. | Preparation of defect-free polyacrylamide electrophoresis gels in plastic cassettes |
| US20080128281A1 (en) * | 2004-11-26 | 2008-06-05 | Ge Healthcare Bio-Sciences Ab | Gel Composite |
| US20090211907A1 (en) * | 2005-02-25 | 2009-08-27 | Japan Science And Technology Agency | Separation Medium for Biochemical Analysis |
| ES2294949B1 (es) * | 2006-09-22 | 2009-04-01 | Universidad De Barcelona | Gel para la separacion de proteinas. |
| US8349167B2 (en) | 2006-12-14 | 2013-01-08 | Life Technologies Corporation | Methods and apparatus for detecting molecular interactions using FET arrays |
| US20080272002A1 (en) * | 2007-05-03 | 2008-11-06 | Protein Forest, Inc. | System and Method for Proteomics |
| DE102008006086A1 (de) * | 2008-01-25 | 2009-09-03 | Evonik Goldschmidt Gmbh | Biomimetische Modellsysteme zur Nachstellung von Spreitungsphänomenen kosmetischer und pharmazeutischer Formulierungen auf menschlicher Haut |
| US20100032296A1 (en) * | 2008-08-07 | 2010-02-11 | Protein Forest, Inc. | Systems and methods for quantitative analyte transfer |
| US8574835B2 (en) * | 2009-05-29 | 2013-11-05 | Life Technologies Corporation | Scaffolded nucleic acid polymer particles and methods of making and using |
| US8653567B2 (en) | 2010-07-03 | 2014-02-18 | Life Technologies Corporation | Chemically sensitive sensor with lightly doped drains |
| US9664646B2 (en) | 2012-11-20 | 2017-05-30 | Bio-Rad Laboratories, Inc. | Polyacrylamide electrophoresis gels with protection against oxygen exposure |
| WO2017172437A1 (en) * | 2016-03-30 | 2017-10-05 | Tufts University | Fabrication of macroporous polymeric hydrogel microparticles |
| CN107266692A (zh) * | 2017-05-12 | 2017-10-20 | 李宗津 | 纳米复合水凝胶材料及制备方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3755280A (en) * | 1971-03-05 | 1973-08-28 | American Cyanamid Co | Drying of acrylamide polymer gels |
| DE3581445D1 (de) * | 1984-07-06 | 1991-02-28 | Fuji Photo Film Co Ltd | Traeger fuer elektrophorese. |
| EP0172723B2 (en) * | 1984-08-15 | 1997-11-05 | Ciba Specialty Chemicals Water Treatments Limited | Water soluble polymers |
| US4746551A (en) * | 1985-11-20 | 1988-05-24 | Micro-Map, Inc. | Rehydratable polyacrylamide gels |
| US5292665A (en) * | 1989-03-15 | 1994-03-08 | The United States Of America As Represented By The Department Of Health And Human Services | Catalyst for preparing polyacrylamide gel which improves the detection of biomaterials by silver staining |
| US5149416A (en) * | 1989-04-18 | 1992-09-22 | Eastman Kodak Company | Polymeric electrophoresis media |
| US5290411A (en) * | 1992-07-14 | 1994-03-01 | California Institute Of Technology | Acrylic polymer electrophoresis support media |
| WO1996009537A1 (en) * | 1994-09-19 | 1996-03-28 | Novel Experimental Technology | Plastic mold for electrophoresis gel |
| AUPO093296A0 (en) * | 1996-07-10 | 1996-08-01 | University Of Melbourne, The | Electrophoresis gels and crosslinking agents for their preparation |
| WO1998052031A1 (en) * | 1997-05-13 | 1998-11-19 | Hoefer Pharmacia Biotech, Inc. | Gel casting and electrophoresis device |
| US6846881B2 (en) * | 2002-02-27 | 2005-01-25 | Bio-Rad Laboratories, Inc. | Preparation of defect-free polyacrylamide electrophoresis gels in plastic cassettes |
-
2002
- 2002-02-27 US US10/087,140 patent/US6846881B2/en not_active Expired - Lifetime
-
2003
- 2003-02-26 DE DE60322027T patent/DE60322027D1/de not_active Expired - Lifetime
- 2003-02-26 EP EP03709407A patent/EP1478670B1/en not_active Expired - Lifetime
- 2003-02-26 WO PCT/US2003/006207 patent/WO2003072616A1/en not_active Ceased
- 2003-02-26 JP JP2003571320A patent/JP4287284B2/ja not_active Expired - Fee Related
- 2003-02-26 CA CA002476768A patent/CA2476768C/en not_active Expired - Fee Related
- 2003-02-26 AU AU2003212467A patent/AU2003212467C1/en not_active Ceased
-
2004
- 2004-10-25 US US10/973,541 patent/US20050059761A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1478670A4 (en) | 2006-03-15 |
| AU2003212467B2 (en) | 2006-01-12 |
| US20030162891A1 (en) | 2003-08-28 |
| WO2003072616A1 (en) | 2003-09-04 |
| AU2003212467A1 (en) | 2003-09-09 |
| AU2003212467C1 (en) | 2006-11-09 |
| JP2005519145A (ja) | 2005-06-30 |
| DE60322027D1 (de) | 2008-08-21 |
| CA2476768A1 (en) | 2003-09-04 |
| CA2476768C (en) | 2008-08-12 |
| US6846881B2 (en) | 2005-01-25 |
| EP1478670A1 (en) | 2004-11-24 |
| US20050059761A1 (en) | 2005-03-17 |
| EP1478670B1 (en) | 2008-07-09 |
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