DE2600891A1 - Verfahren zur herstellung von getrockneten rehydratisierbaren agarose- oder gelose-enthaltenden platten - Google Patents
Verfahren zur herstellung von getrockneten rehydratisierbaren agarose- oder gelose-enthaltenden plattenInfo
- Publication number
- DE2600891A1 DE2600891A1 DE19762600891 DE2600891A DE2600891A1 DE 2600891 A1 DE2600891 A1 DE 2600891A1 DE 19762600891 DE19762600891 DE 19762600891 DE 2600891 A DE2600891 A DE 2600891A DE 2600891 A1 DE2600891 A1 DE 2600891A1
- Authority
- DE
- Germany
- Prior art keywords
- agarose
- copolymer
- gelose
- aqueous
- linear
- 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
- 229920000936 Agarose Polymers 0.000 title claims description 41
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 39
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 31
- 229920001577 copolymer Polymers 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 24
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 23
- 235000011187 glycerol Nutrition 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 11
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 11
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 108010025899 gelatin film Proteins 0.000 claims description 9
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims description 7
- 229920005684 linear copolymer Polymers 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 150000002894 organic compounds Chemical class 0.000 claims description 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 4
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 238000007334 copolymerization reaction Methods 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 238000001962 electrophoresis Methods 0.000 claims description 3
- 230000000951 immunodiffusion Effects 0.000 claims description 3
- 238000000760 immunoelectrophoresis Methods 0.000 claims description 3
- 239000002609 medium Substances 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- 150000003077 polyols Chemical class 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 208000023514 Barrett esophagus Diseases 0.000 claims 1
- 239000000499 gel Substances 0.000 description 25
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 229920002401 polyacrylamide Polymers 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- 238000004321 preservation Methods 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 229920000298 Cellophane Polymers 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000872 buffer Substances 0.000 description 4
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000004552 water soluble powder Substances 0.000 description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- FTOAOBMCPZCFFF-UHFFFAOYSA-N 5,5-diethylbarbituric acid Chemical compound CCC1(CC)C(=O)NC(=O)NC1=O FTOAOBMCPZCFFF-UHFFFAOYSA-N 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- 229920006322 acrylamide copolymer Polymers 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- MTPJEFOSTIKRSS-UHFFFAOYSA-N 3-(dimethylamino)propanenitrile Chemical compound CN(C)CCC#N MTPJEFOSTIKRSS-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229960002319 barbital Drugs 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000004281 calcium formate Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- -1 for example a polyol Chemical class 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000001665 trituration Methods 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/12—Agar or agar-agar, i.e. mixture of agarose and agaropectin; Derivatives thereof
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
- Y10T428/31736—Next to polyester
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
- Y10T428/31797—Next to addition polymer from unsaturated monomers
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)
- Physics & Mathematics (AREA)
- Dispersion Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Electrochemistry (AREA)
- Pathology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7500922A FR2297879A1 (fr) | 1975-01-14 | 1975-01-14 | Procede de preparation de plaques sechees rehydratables contenant de l'agarose ou de la gelose |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2600891A1 true DE2600891A1 (de) | 1976-11-18 |
Family
ID=9149714
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19762600891 Ceased DE2600891A1 (de) | 1975-01-14 | 1976-01-12 | Verfahren zur herstellung von getrockneten rehydratisierbaren agarose- oder gelose-enthaltenden platten |
Country Status (7)
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2826895A1 (de) * | 1978-06-19 | 1980-01-03 | Sebia Sa | Platten fuer die elektrophoretische trennung von lipoproteinen und verfahren zu ihrer herstellung |
EP0087995A1 (en) * | 1982-02-19 | 1983-09-07 | FMC Corporation | Copolymer of acrylamide and polysaccharide resin as electrophoretic gel medium |
EP0115436A3 (en) * | 1983-01-26 | 1984-11-07 | Fuji Photo Film Co., Ltd. | Medium for electrophoresis |
EP0139471A3 (en) * | 1983-09-14 | 1987-04-22 | Fuji Photo Film Co., Ltd. | Medium for electrophoresis |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2378808A1 (fr) * | 1977-01-28 | 1978-08-25 | Mar Pha Etu Expl Marques | Nouveaux copolymeres hydrophiles a base de n-(tris(hydroxy-methyl)methyl)acrylamide ou de n-(tris (hydroxymethyl)methyl)methacrylamide, leur preparation et leur emploi dans les techniques de separation |
AT371723B (de) * | 1978-11-15 | 1983-07-25 | Max Planck Gesellschaft | Transparentes fluessigkeitsverbandmaterial, und verfahren zu seiner herstellung |
JPS59126236A (ja) * | 1983-01-08 | 1984-07-20 | Fuji Photo Film Co Ltd | 電気泳動用媒体 |
US5080809A (en) * | 1983-01-28 | 1992-01-14 | Phillips Petroleum Company | Polymers useful in the recovery and processing of natural resources |
US5186257A (en) * | 1983-01-28 | 1993-02-16 | Phillips Petroleum Company | Polymers useful in the recovery and processing of natural resources |
US4791063A (en) * | 1983-02-14 | 1988-12-13 | Cuno Incorporated | Polyionene transformed modified polysaccharide supports |
JPS59166850A (ja) * | 1983-03-11 | 1984-09-20 | Fuji Photo Film Co Ltd | 電気泳動用媒体材料 |
JPS59164950A (ja) * | 1983-03-11 | 1984-09-18 | Fuji Photo Film Co Ltd | 電気泳動用媒体材料 |
US4499214A (en) * | 1983-05-03 | 1985-02-12 | Diachem Industries, Inc. | Method of rapidly dissolving polymers in water |
EP0155833A3 (en) * | 1984-03-15 | 1988-07-27 | Fuji Photo Film Co., Ltd. | Element for electrophoresis |
GB8428876D0 (en) * | 1984-11-15 | 1984-12-27 | Ciba Geigy Ag | Diagnostic strips |
GB8514052D0 (en) * | 1985-06-04 | 1985-07-10 | Geistlich Soehne Ag | Compositions |
FR2601026B1 (fr) * | 1986-04-15 | 1988-09-16 | Rhone Poulenc Chimie | Matiere seche hydratable en un gel aqueux contenant des particules de polymeres dispersees, procede pour sa preparation et son application en biologie |
US4897306A (en) * | 1986-04-19 | 1990-01-30 | Fuji Photo Film Co., Ltd. | Medium for electrophoresis |
FR2630456B1 (fr) * | 1988-04-26 | 1990-08-10 | Kaysersberg Sa | Milieu de culture, notamment utilisable en culture in vitro et en bacteriologie; son procede de preparation |
US4999340A (en) * | 1988-08-04 | 1991-03-12 | Board Of Regents, The University Of Texas System | Rehydratable agarose gels |
US5149416A (en) * | 1989-04-18 | 1992-09-22 | Eastman Kodak Company | Polymeric electrophoresis media |
US5443704A (en) * | 1991-12-31 | 1995-08-22 | Fmc Corporation | Electrophoresis gel container assemblies |
US6358385B1 (en) * | 1993-12-17 | 2002-03-19 | The Perkin-Elmer Corporation | Polymers for separation of biomolecules by capillary electrophoresis |
AU1254295A (en) * | 1993-12-17 | 1995-07-03 | Perkin-Elmer Corporation, The | Uncharged polymers for separation of biomolecules by capillary electrophoresis |
US6355709B1 (en) * | 1993-12-17 | 2002-03-12 | The Perkin-Elmer Corporation | Polymers for separation of biomolecules by capillary electrophoresis |
US5503722A (en) * | 1994-02-28 | 1996-04-02 | Beckman Instruments, Inc. | Rehydratable gels for capillary electrophoresis |
US5747600A (en) * | 1994-06-24 | 1998-05-05 | Fang; Ta-Yun | Reconstitutable polyacrylamide materials and methods for producing same |
CA2358480A1 (en) * | 1999-01-12 | 2000-07-20 | Spectrumedix Corporation | Copolymers for capillary gel electrophoresis |
US7201833B2 (en) * | 2001-06-04 | 2007-04-10 | Epocal Inc. | Integrated solid-phase hydrophilic matrix circuits and micro-arrays |
US7214300B2 (en) * | 2001-06-04 | 2007-05-08 | Epocal Inc. | Integrated electrokinetic devices and methods of manufacture |
US20030220632A1 (en) * | 2002-05-23 | 2003-11-27 | Wolfgang Strasser | Method of using gel sheets for laser treatment |
US20040060855A1 (en) * | 2002-09-30 | 2004-04-01 | University Of Alabama | Countercurrent web contactor for use in separation of biological agents |
US20200060957A1 (en) | 2018-08-27 | 2020-02-27 | Lonza Ltd | Dried Rehydratable Composition |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1483742A (fr) * | 1965-11-30 | 1967-06-09 | Centre Nat Rech Scient | Gels mixtes d'acrylamide-agarose, procédé pour leur préparation et leurs applications |
-
1975
- 1975-01-14 FR FR7500922A patent/FR2297879A1/fr active Granted
-
1976
- 1976-01-12 DE DE19762600891 patent/DE2600891A1/de not_active Ceased
- 1976-01-12 US US05/648,084 patent/US4048377A/en not_active Expired - Lifetime
- 1976-01-13 CH CH32776A patent/CH606202A5/xx not_active IP Right Cessation
- 1976-01-13 SE SE7600299A patent/SE429343B/xx unknown
- 1976-01-13 GB GB1119/76A patent/GB1541712A/en not_active Expired
- 1976-01-14 IT IT67074/76A patent/IT1055788B/it active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1483742A (fr) * | 1965-11-30 | 1967-06-09 | Centre Nat Rech Scient | Gels mixtes d'acrylamide-agarose, procédé pour leur préparation et leurs applications |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2826895A1 (de) * | 1978-06-19 | 1980-01-03 | Sebia Sa | Platten fuer die elektrophoretische trennung von lipoproteinen und verfahren zu ihrer herstellung |
EP0087995A1 (en) * | 1982-02-19 | 1983-09-07 | FMC Corporation | Copolymer of acrylamide and polysaccharide resin as electrophoretic gel medium |
EP0115436A3 (en) * | 1983-01-26 | 1984-11-07 | Fuji Photo Film Co., Ltd. | Medium for electrophoresis |
EP0139471A3 (en) * | 1983-09-14 | 1987-04-22 | Fuji Photo Film Co., Ltd. | Medium for electrophoresis |
Also Published As
Publication number | Publication date |
---|---|
FR2297879B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-03-17 |
SE7600299L (sv) | 1976-07-15 |
GB1541712A (en) | 1979-03-07 |
IT1055788B (it) | 1982-01-11 |
SE429343B (sv) | 1983-08-29 |
US4048377A (en) | 1977-09-13 |
FR2297879A1 (fr) | 1976-08-13 |
CH606202A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-10-31 |
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