SE436759B - Forfarande for bestemning av alfa-amylas - Google Patents
Forfarande for bestemning av alfa-amylasInfo
- Publication number
- SE436759B SE436759B SE7902238A SE7902238A SE436759B SE 436759 B SE436759 B SE 436759B SE 7902238 A SE7902238 A SE 7902238A SE 7902238 A SE7902238 A SE 7902238A SE 436759 B SE436759 B SE 436759B
- Authority
- SE
- Sweden
- Prior art keywords
- starch
- group
- process according
- coupling
- dye
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 19
- 229920000881 Modified starch Polymers 0.000 claims description 30
- 235000019426 modified starch Nutrition 0.000 claims description 30
- 229920002472 Starch Polymers 0.000 claims description 25
- 239000008107 starch Substances 0.000 claims description 25
- 235000019698 starch Nutrition 0.000 claims description 23
- 238000003776 cleavage reaction Methods 0.000 claims description 16
- 230000007017 scission Effects 0.000 claims description 16
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 230000015572 biosynthetic process Effects 0.000 claims description 15
- 238000005859 coupling reaction Methods 0.000 claims description 13
- 230000008878 coupling Effects 0.000 claims description 12
- 238000010168 coupling process Methods 0.000 claims description 12
- 238000000502 dialysis Methods 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 10
- 238000005691 oxidative coupling reaction Methods 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000004382 Amylase Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 102000013142 Amylases Human genes 0.000 claims description 4
- 108010065511 Amylases Proteins 0.000 claims description 4
- 235000019418 amylase Nutrition 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 claims description 4
- 238000000926 separation method Methods 0.000 claims description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- HJXIRCMNJLIHQR-UHFFFAOYSA-N 2-n,2-n-dimethylbenzene-1,2-diamine Chemical compound CN(C)C1=CC=CC=C1N HJXIRCMNJLIHQR-UHFFFAOYSA-N 0.000 claims description 3
- 150000001448 anilines Chemical class 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000007857 hydrazones Chemical class 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical group CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- IHDBZCJYSHDCKF-UHFFFAOYSA-N 4,6-dichlorotriazine Chemical group ClC1=CC(Cl)=NN=N1 IHDBZCJYSHDCKF-UHFFFAOYSA-N 0.000 claims description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical group CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 claims description 2
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 2
- 238000005119 centrifugation Methods 0.000 claims description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- ZBKFYXZXZJPWNQ-UHFFFAOYSA-N isothiocyanate group Chemical group [N-]=C=S ZBKFYXZXZJPWNQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000466 oxiranyl group Chemical group 0.000 claims description 2
- -1 potassium ferricyanide Chemical compound 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 2
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 2
- 125000005490 tosylate group Chemical group 0.000 claims description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000007822 coupling agent Substances 0.000 claims 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 210000002268 wool Anatomy 0.000 claims 1
- 239000000975 dye Substances 0.000 description 25
- 239000000243 solution Substances 0.000 description 13
- 239000007788 liquid Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 230000008033 biological extinction Effects 0.000 description 8
- 239000012528 membrane Substances 0.000 description 8
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- 239000012634 fragment Substances 0.000 description 6
- 238000011534 incubation Methods 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004366 Glucose oxidase Substances 0.000 description 3
- 108010015776 Glucose oxidase Proteins 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229940116332 glucose oxidase Drugs 0.000 description 3
- 235000019420 glucose oxidase Nutrition 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000001254 oxidized starch Substances 0.000 description 3
- 235000013808 oxidized starch Nutrition 0.000 description 3
- 239000008363 phosphate buffer Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000011218 segmentation Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 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 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 102000003992 Peroxidases Human genes 0.000 description 1
- 229920000473 Phlobaphene Polymers 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 229960000212 aminophenazone Drugs 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000012928 buffer substance Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000007979 citrate buffer Substances 0.000 description 1
- 101150061397 cnfn gene Proteins 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 125000001752 diazonium salt group Chemical group 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/34—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
- C12Q1/40—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase involving amylase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2334/00—O-linked chromogens for determinations of hydrolase enzymes, e.g. glycosidases, phosphatases, esterases
-
- 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
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/805—Test papers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Analytical Chemistry (AREA)
- Biophysics (AREA)
- Polymers & Plastics (AREA)
- Biotechnology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2812154A DE2812154C3 (de) | 1978-03-20 | 1978-03-20 | Verfahren zur Bestimmung von a -Amylase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE7902238L SE7902238L (sv) | 1979-09-21 |
| SE436759B true SE436759B (sv) | 1985-01-21 |
Family
ID=6034977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7902238A SE436759B (sv) | 1978-03-20 | 1979-03-13 | Forfarande for bestemning av alfa-amylas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4268628A (de) |
| JP (1) | JPS5587A (de) |
| AT (1) | AT363612B (de) |
| BE (1) | BE874944A (de) |
| CH (1) | CH640003A5 (de) |
| DE (1) | DE2812154C3 (de) |
| ES (1) | ES478624A1 (de) |
| FR (1) | FR2420759A1 (de) |
| GB (1) | GB2017908B (de) |
| IT (1) | IT1166710B (de) |
| NL (1) | NL7901699A (de) |
| SE (1) | SE436759B (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3001878A1 (de) * | 1980-01-19 | 1981-07-23 | Behringwerke Ag, 3550 Marburg | Polysaccharid-derivate, verfahren zu ihrer herstellung, ihre verwendung sowie diese enthaltende mittel |
| US4550077A (en) * | 1980-05-07 | 1985-10-29 | Electro-Nucleonics, Inc. | β-Amylase determination |
| JPS632085Y2 (de) * | 1981-01-16 | 1988-01-20 | ||
| US4473471A (en) * | 1982-09-13 | 1984-09-25 | Purolator Inc. | Filter sealing gasket with reinforcement ring |
| JPS6218783A (ja) * | 1985-07-17 | 1987-01-27 | Sharp Corp | 半導体レ−ザ素子 |
| DE3525926A1 (de) | 1985-07-19 | 1987-01-29 | Boehringer Mannheim Gmbh | Verfahren und reagenz zur spezifischen bestimmung von pankreas-alpha-amylase |
| US4950593A (en) * | 1986-08-15 | 1990-08-21 | Vitek Systems, Inc. | Improved method for assaying proteolytic enzymes |
| USRE34284E (en) * | 1986-08-15 | 1993-06-15 | Biomerieux Vitek, Inc. | Method for assaying proteolytic enzymes |
| EP0310940B1 (de) * | 1987-09-30 | 1994-11-23 | Fujirebio Kabushiki Kaisha | Analytische Vorrichtung für enzymimmunologische Tests |
| GB2506695B (en) | 2012-10-02 | 2015-01-07 | Tate & Lyle Ingredients | Process for preparing an inhibited starch |
| AR099935A1 (es) * | 2014-04-15 | 2016-08-31 | Dow Global Technologies Llc | Reactivo de prueba estabilizado |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2317752A (en) * | 1939-10-30 | 1943-04-27 | Nat Starch Products Inc | Modified starch |
| US3117105A (en) * | 1960-07-07 | 1964-01-07 | Miles Lab | Dialdehyde polysaccharide-phenol derivatives |
| US3219518A (en) * | 1963-03-28 | 1965-11-23 | Hercules Powder Co Ltd | Reaction product of dialdehyde with starch ether in paper |
| US3694318A (en) * | 1968-08-19 | 1972-09-26 | Bernard Klein | Substrate and method for alpha-amylase assay |
| US3679661A (en) * | 1970-12-21 | 1972-07-25 | Warner Lambert Co | Preparation of water-soluble,dyed substrates for amylase assay |
| US3888739A (en) * | 1973-05-07 | 1975-06-10 | Bio Reagents & Diagnostics Inc | Reagents and methods for determining amylase concentrations |
| JPS5618198B2 (de) * | 1973-09-21 | 1981-04-27 | ||
| JPS5252691A (en) * | 1975-10-24 | 1977-04-27 | Wako Pure Chem Ind Ltd | Method of determining activity value of leucin amino eptidase |
| US4025392A (en) * | 1976-04-14 | 1977-05-24 | The United States Of America As Represented By The Secretary Of Agriculture | Chromogenic substrate for determination of amylase activity |
| CA1095819A (en) * | 1977-01-14 | 1981-02-17 | Eastman Kodak Company | Element for analysis of liquids |
-
1978
- 1978-03-20 DE DE2812154A patent/DE2812154C3/de not_active Expired
-
1979
- 1979-02-14 AT AT0113179A patent/AT363612B/de not_active IP Right Cessation
- 1979-03-02 NL NL7901699A patent/NL7901699A/xx not_active Application Discontinuation
- 1979-03-09 FR FR7906144A patent/FR2420759A1/fr active Granted
- 1979-03-13 SE SE7902238A patent/SE436759B/sv unknown
- 1979-03-14 ES ES478624A patent/ES478624A1/es not_active Expired
- 1979-03-15 CH CH246879A patent/CH640003A5/de not_active IP Right Cessation
- 1979-03-16 IT IT21092/79A patent/IT1166710B/it active
- 1979-03-19 US US06/022,011 patent/US4268628A/en not_active Expired - Lifetime
- 1979-03-19 GB GB7909523A patent/GB2017908B/en not_active Expired
- 1979-03-19 BE BE0/194096A patent/BE874944A/xx not_active IP Right Cessation
- 1979-03-20 JP JP3186179A patent/JPS5587A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| SE7902238L (sv) | 1979-09-21 |
| BE874944A (fr) | 1979-09-19 |
| FR2420759A1 (fr) | 1979-10-19 |
| JPS5730000B2 (de) | 1982-06-25 |
| NL7901699A (nl) | 1979-09-24 |
| CH640003A5 (de) | 1983-12-15 |
| IT7921092A0 (it) | 1979-03-16 |
| IT1166710B (it) | 1987-05-06 |
| GB2017908A (en) | 1979-10-10 |
| FR2420759B1 (de) | 1983-06-24 |
| JPS5587A (en) | 1980-01-05 |
| DE2812154A1 (de) | 1979-09-27 |
| AT363612B (de) | 1981-08-25 |
| GB2017908B (en) | 1983-03-30 |
| DE2812154B2 (de) | 1980-01-17 |
| ATA113179A (de) | 1981-01-15 |
| US4268628A (en) | 1981-05-19 |
| ES478624A1 (es) | 1979-06-01 |
| DE2812154C3 (de) | 1980-09-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SE436759B (sv) | Forfarande for bestemning av alfa-amylas | |
| CA1155737A (en) | Process and diagnostic agents for the detection of redox reactions | |
| CN100357449C (zh) | 用于分光光度法测定分析物的染料偶合对 | |
| CA2192744C (en) | Stable coupling dye for photometric determination of analytes | |
| US3668076A (en) | Diagnostic agent | |
| US11814669B2 (en) | Blood sample assay method | |
| CN103558189B (zh) | 用于检测被湿度损害的尿测试条的装置和方法 | |
| US8574896B2 (en) | Colorimetric method and reagent used for the same | |
| JPS6112669A (ja) | アミノピラゾリノン、その製法およびｈ↓２ｏ↓２検出法 | |
| SE445829B (sv) | Ny l-gamma-glutamyl-3-karboxi-4-hydroxianilid och salter derav | |
| JPH0427839B2 (de) | ||
| US5013647A (en) | Removal of interfering reducing substances with tetrazolium salts in redox measurement reactions | |
| EP0152274B1 (de) | Verfahren zur Bestimmung von Leucinaminopeptidase (LAP) | |
| US20040132200A1 (en) | Fluorescent creatinine assay | |
| CN112710609A (zh) | 抗乳糜干扰的尿酸测定试剂盒 | |
| JP5231063B2 (ja) | 酸化発色化合物の製造方法 | |
| CN112525901B (zh) | 一种硫酸铜中铜含量的测定方法 | |
| CN111103342A (zh) | 一种高精度抗干扰性能强的肌酐丝网印刷电极制备方法 | |
| KR0147861B1 (ko) | 인체 뇨중의 백혈구 측정용 간이시험지와 그의 제조방법 | |
| EP0255708A2 (de) | Indikatorzusammensetzung und Verfahren zu ihrer Herstellung | |
| WO2023190714A1 (ja) | リゾホスホリパーゼｄの活性測定方法、リゾホスホリパーゼｄ活性測定用感度向上剤、組成物、及び、キット | |
| CN105695582A (zh) | 一种非综合征耳聋基因检测膜条以及pcr引物 | |
| CN104603282A (zh) | 高密度脂蛋白中的胆固醇的测定方法 | |
| CN111337674A (zh) | 一种用于预测心血管事件风险的试剂盒 | |
| JPH05130897A (ja) | チオール化合物測定用試薬組成物 |