LU81699A1 - Gels d'agarose conditionnee dans des tubes metalliques - Google Patents

Gels d'agarose conditionnee dans des tubes metalliques Download PDF

Info

Publication number: LU81699A1
Authority: LU; Luxembourg
Prior art keywords: weight; aqueous gels; aqueous; gels according; gel
Prior art date: 1978-09-22

Application number

LU81699A

Other languages

English (en)

French (fr)

Inventor

E Boschetti

Original Assignee

Pharmindustrie

Priority date (The priority date 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 date listed.)

1978-09-22

Filing date

1979-09-19

Publication date

1981-04-17

1979-09-19 Application filed by Pharmindustrie filed Critical Pharmindustrie

1981-04-17 Publication of LU81699A1 publication Critical patent/LU81699A1/fr

Links

239000000499 gel Substances 0.000 title claims description 92
229910052751 metal Inorganic materials 0.000 title claims description 9
239000002184 metal Substances 0.000 title claims description 9
230000001143 conditioned effect Effects 0.000 title 1
229920000936 Agarose Polymers 0.000 claims description 30
229920001817 Agar Polymers 0.000 claims description 20
235000010419 agar Nutrition 0.000 claims description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
239000000872 buffer Substances 0.000 claims description 18
241000206672 Gelidium Species 0.000 claims description 16
238000000034 method Methods 0.000 claims description 16
238000001962 electrophoresis Methods 0.000 claims description 10
238000000760 immunoelectrophoresis Methods 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 9
235000018102 proteins Nutrition 0.000 claims description 9
108090000623 proteins and genes Proteins 0.000 claims description 9
102000004169 proteins and genes Human genes 0.000 claims description 9
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 claims description 8
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 claims description 8
239000000203 mixture Substances 0.000 claims description 8
239000000600 sorbitol Substances 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
125000000524 functional group Chemical group 0.000 claims description 5
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 4
229930195725 Mannitol Natural products 0.000 claims description 4
230000002255 enzymatic effect Effects 0.000 claims description 4
239000000594 mannitol Substances 0.000 claims description 4
235000010355 mannitol Nutrition 0.000 claims description 4
125000003277 amino group Chemical group 0.000 claims description 3
238000001155 isoelectric focusing Methods 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
229920003169 water-soluble polymer Polymers 0.000 claims description 3
108010010803 Gelatin Proteins 0.000 claims description 2
229920002472 Starch Polymers 0.000 claims description 2
229930006000 Sucrose Natural products 0.000 claims description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
230000002378 acidificating effect Effects 0.000 claims description 2
150000007513 acids Chemical class 0.000 claims description 2
GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
239000005018 casein Substances 0.000 claims description 2
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims description 2
235000021240 caseins Nutrition 0.000 claims description 2
238000009792 diffusion process Methods 0.000 claims description 2
239000008273 gelatin Substances 0.000 claims description 2
229920000159 gelatin Polymers 0.000 claims description 2
235000019322 gelatine Nutrition 0.000 claims description 2
235000011852 gelatine desserts Nutrition 0.000 claims description 2
230000000951 immunodiffusion Effects 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
239000008107 starch Substances 0.000 claims description 2
235000019698 starch Nutrition 0.000 claims description 2
239000005720 sucrose Substances 0.000 claims description 2
-1 alicyclic carboxylic acid Chemical class 0.000 claims 1
239000000022 bacteriostatic agent Substances 0.000 claims 1
229920000642 polymer Polymers 0.000 claims 1
239000000243 solution Substances 0.000 description 28
FTOAOBMCPZCFFF-UHFFFAOYSA-N 5,5-diethylbarbituric acid Chemical compound CCC1(CC)C(=O)NC(=O)NC1=O FTOAOBMCPZCFFF-UHFFFAOYSA-N 0.000 description 15
229960002319 barbital Drugs 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
238000003756 stirring Methods 0.000 description 8
239000007983 Tris buffer Substances 0.000 description 7
235000010356 sorbitol Nutrition 0.000 description 7
229960002920 sorbitol Drugs 0.000 description 7
238000009835 boiling Methods 0.000 description 6
239000000470 constituent Substances 0.000 description 6
239000011543 agarose gel Substances 0.000 description 5
229920002401 polyacrylamide Polymers 0.000 description 5
RGHFKWPGWBFQLN-UHFFFAOYSA-M sodium;5,5-diethylpyrimidin-3-ide-2,4,6-trione Chemical compound [Na+].CCC1(CC)C([O-])=NC(=O)NC1=O RGHFKWPGWBFQLN-UHFFFAOYSA-M 0.000 description 5
238000001816 cooling Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 4
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 3
239000008272 agar Substances 0.000 description 3
238000001879 gelation Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
230000036571 hydration Effects 0.000 description 3
238000006703 hydration reaction Methods 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
230000003385 bacteriostatic effect Effects 0.000 description 2
239000012954 diazonium Substances 0.000 description 2
150000001989 diazonium salts Chemical class 0.000 description 2
229960001031 glucose Drugs 0.000 description 2
239000008103 glucose Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
238000010258 microfractionation Methods 0.000 description 2
229920005615 natural polymer Polymers 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
239000002966 varnish Substances 0.000 description 2
AVYGCQXNNJPXSS-UHFFFAOYSA-N 2,5-dichloroaniline Chemical compound NC1=CC(Cl)=CC=C1Cl AVYGCQXNNJPXSS-UHFFFAOYSA-N 0.000 description 1
JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
102000002260 Alkaline Phosphatase Human genes 0.000 description 1
108020004774 Alkaline Phosphatase Proteins 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
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 1
229910019142 PO4 Inorganic materials 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
229920004890 Triton X-100 Polymers 0.000 description 1
239000013504 Triton X-100 Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000007982 barbital buffer Substances 0.000 description 1
229960000796 barbital sodium Drugs 0.000 description 1
235000013405 beer Nutrition 0.000 description 1
ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 1
MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
229960002401 calcium lactate Drugs 0.000 description 1
235000011086 calcium lactate Nutrition 0.000 description 1
239000001527 calcium lactate Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000004113 cell culture Methods 0.000 description 1
229960003260 chlorhexidine Drugs 0.000 description 1
OSASVXMJTNOKOY-UHFFFAOYSA-N chlorobutanol Chemical compound CC(C)(O)C(Cl)(Cl)Cl OSASVXMJTNOKOY-UHFFFAOYSA-N 0.000 description 1
229960004926 chlorobutanol Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
235000014510 cooky Nutrition 0.000 description 1
230000007423 decrease Effects 0.000 description 1
229960003964 deoxycholic acid Drugs 0.000 description 1
229960001484 edetic acid Drugs 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
QMMMCTXNYMSXLI-UHFFFAOYSA-N fast blue B Chemical compound C1=C([N+]#N)C(OC)=CC(C=2C=C(OC)C([N+]#N)=CC=2)=C1 QMMMCTXNYMSXLI-UHFFFAOYSA-N 0.000 description 1
238000001914 filtration Methods 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
239000008187 granular material Substances 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
IZXGZAJMDLJLMF-UHFFFAOYSA-N methylaminomethanol Chemical compound CNCO IZXGZAJMDLJLMF-UHFFFAOYSA-N 0.000 description 1
CNXZLZNEIYFZGU-UHFFFAOYSA-N n-(4-amino-2,5-diethoxyphenyl)benzamide Chemical compound C1=C(N)C(OCC)=CC(NC(=O)C=2C=CC=CC=2)=C1OCC CNXZLZNEIYFZGU-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000002674 ointment Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
FHHPUSMSKHSNKW-SMOYURAASA-M sodium deoxycholate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 FHHPUSMSKHSNKW-SMOYURAASA-M 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000010409 thin film Substances 0.000 description 1
229920003170 water-soluble synthetic polymer Polymers 0.000 description 1

Classifications

- 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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Molecular Biology (AREA)
Biochemistry (AREA)
General Physics & Mathematics (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Electrochemistry (AREA)
Physics & Mathematics (AREA)
Analytical Chemistry (AREA)
Medicinal Chemistry (AREA)
General Health & Medical Sciences (AREA)
Dispersion Chemistry (AREA)
Immunology (AREA)
Pathology (AREA)
Cosmetics (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Jellies, Jams, And Syrups (AREA)
Medicinal Preparation (AREA)
Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Colloid Chemistry (AREA)

LU81699A 1978-09-22 1979-09-19 Gels d'agarose conditionnee dans des tubes metalliques LU81699A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR7827179		1978-09-22
FR7827179A FR2436791A1 (fr)	1978-09-22	1978-09-22	Gels d'agarose conditionnes dans des tubes metalliques

Publications (1)

Publication Number	Publication Date
LU81699A1 true LU81699A1 (fr)	1981-04-17

Family

ID=9212916

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU81699A LU81699A1 (fr)	1978-09-22	1979-09-19	Gels d'agarose conditionnee dans des tubes metalliques

Country Status (12)

Country	Link
EP (1)	EP0009430B1 (de)
JP (1)	JPS5544396A (de)
AT (1)	ATA615579A (de)
BE (1)	BE878846A (de)
CA (1)	CA1143681A (de)
CH (1)	CH643575A5 (de)
DE (1)	DE2962292D1 (de)
FR (1)	FR2436791A1 (de)
IT (1)	IT1119166B (de)
LU (1)	LU81699A1 (de)
PT (1)	PT70194A (de)
SE (1)	SE7907857L (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS59126236A (ja) *	1983-01-08	1984-07-20	Fuji Photo Film Co Ltd	電気泳動用媒体
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
CH666907A5 (fr) *	1985-11-13	1988-08-31	Medinational Harley Street Lim	Procede de preparation d'un complexe de polygalactane macromoleculaire et de compose azote, et utilisation de ce complexe.
DE3737815A1 (de) *	1987-11-06	1989-05-18	Wacker Chemitronic	Siliciumscheiben zur erzeugung von oxidschichten hoher durchschlagsfestigkeit und verfahren zur ihrer herstellung
US5068019A (en) *	1989-05-19	1991-11-26	Fuji Photo Film Co., Ltd.	Electrophoresis film support
DE3935020A1 (de) *	1989-10-20	1991-04-25	Serva Feinbiochem Gmbh & Co	Verbesserte elektrophoresegele aus agarose

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
USRE26199E (en) *		1967-05-09		Agar preparation and process of producing the same
US2963373A (en) *	1958-11-17	1960-12-06	American Molasses Company	Icings and method of preparing them and cold-water soluble agar and carrageen gums for said icings
BE666282A (de) *	1966-04-18
US3766047A (en) *	1972-09-11	1973-10-16	F Elevitch	Gel for electrophoresis

1978
- 1978-09-22 FR FR7827179A patent/FR2436791A1/fr active Granted
1979
- 1979-09-04 EP EP79400607A patent/EP0009430B1/de not_active Expired
- 1979-09-04 DE DE7979400607T patent/DE2962292D1/de not_active Expired
- 1979-09-18 PT PT70194A patent/PT70194A/pt unknown
- 1979-09-18 BE BE0/197191A patent/BE878846A/fr not_active IP Right Cessation
- 1979-09-19 LU LU81699A patent/LU81699A1/fr unknown
- 1979-09-19 AT AT0615579A patent/ATA615579A/de not_active Application Discontinuation
- 1979-09-20 CH CH849779A patent/CH643575A5/fr not_active IP Right Cessation
- 1979-09-20 CA CA000336039A patent/CA1143681A/fr not_active Expired
- 1979-09-20 IT IT68841/79A patent/IT1119166B/it active
- 1979-09-21 JP JP12188279A patent/JPS5544396A/ja active Pending
- 1979-09-21 SE SE7907857A patent/SE7907857L/ not_active Application Discontinuation

Also Published As

Publication number	Publication date
SE7907857L (sv)	1980-03-23
CA1143681A (fr)	1983-03-29
IT7968841A0 (it)	1979-09-20
FR2436791A1 (fr)	1980-04-18
FR2436791B1 (de)	1981-02-13
IT1119166B (it)	1986-03-03
JPS5544396A (en)	1980-03-28
DE2962292D1 (en)	1982-04-15
BE878846A (fr)	1980-03-18
EP0009430B1 (de)	1982-03-17
PT70194A (fr)	1979-10-01
CH643575A5 (fr)	1984-06-15
EP0009430A1 (de)	1980-04-02
ATA615579A (de)	1984-05-15

Publication	Publication Date	Title
US4008321A (en)	1977-02-15	Composition for a topical preparation and a process for producing the same
LU81699A1 (fr)	1981-04-17	Gels d'agarose conditionnee dans des tubes metalliques
EP0155427B1 (de)	1988-05-04	Gebrauchsfertiger schnellauflöslicher fester Nährboden und Verfahren zu seiner Herstellung
LU81917A1 (fr)	1980-04-22	Enzyme immobilise,son procede de preparation et procede pour realiser une reaction enzymatique
JPH1036676A (ja)	1998-02-10	タンパク質水溶液の濃縮方法
FR2546717A1 (fr)	1984-12-07	Procede pour realiser des materiaux biologiques souples rendus inalterables et contenant ou non un agent conservateur
EP3921372B1 (de)	2022-09-21	Proteinhydrogel, herstellungsverfahren und verwendung davon
EP0067074B1 (de)	1984-08-01	Wasserabweisender Zusatzstoff für Gips und gipshaltige Produkte und Verfahren zum Wasserabweisendmachen
FR2575833A1 (fr)	1986-07-11	Procede de fabrication de bandes pour diagnostic, bandes obtenues et utilisation de telles bandes comme support reactif dans une technique d'electrophorese ou de focalisation isoelectrique
JPS61152247A (ja)	1986-07-10	蛋白質膜の製造法
Kirkeby et al.	1986	Studies on the actions of glutaraldehyde, formaldehyde, and mixtures of glutaraldehyde and formaldehyde on tissue proteins
CA2394241C (fr)	2006-05-23	Procede d'additivation minimisant la segregation des additifs et leur migration
FR2538907A1 (fr)	1984-07-06	Reactif immunologique constitue par des antigenes ou des anticorps en forme de cellules des particules ou des molecules ancres sur des surfaces solides continues par des unions ioniques ou covalents
RU2078110C1 (ru)	1997-04-27	Клей для сигаретной промышленности и способ его получения
FR2577563A1 (fr)	1986-08-22	Composition hydroretentrice stabilisee a base de polyelectrolyte hydrocolloidal reticule
RU2078109C1 (ru)	1997-04-27	Клей для сигаретной промышленности и способ его получения
US274979A (en)	1883-04-03	Adhesive paste
EP1172036B1 (de)	2006-04-26	Verfahren zur Pasteurisierung einer flüssigen Zusammensetzung auf Eierbasis
FR2619219A1 (fr)	1989-02-10	Reactif sec pour la determination de la lipase pancreatique, procede de preparation dudit reactif sec et reactif sec et reactif sous forme d'emulsion obtenu par reconstitution du reactif sec.
FR3115961A1 (fr)	2022-05-13	Solution virucide de lavage des mains et procede de preparation
SU1587030A1 (ru)	1990-08-23	Сложное гранулированное удобрение продленного действи с микроэлементами
AU747859B2 (en)	2002-05-23	Gelling agents and gels containing them
FR2510760A1 (fr)	1983-02-04	Dosage de folates par fixation competitive de proteines perfectionne et jeu de reactifs pour sa mise en oeuvre
JPS62244437A (ja)	1987-10-24	ゲル製造基材
EP0585804A1 (de)	1994-03-09	NaOH enthaltende Hühneraugenmittel