SE436894B - Sett att samtidigt bestemma transaminaser (got och gpt) med kinetisk uv-metod - Google Patents
Sett att samtidigt bestemma transaminaser (got och gpt) med kinetisk uv-metodInfo
- Publication number
- SE436894B SE436894B SE8005122A SE8005122A SE436894B SE 436894 B SE436894 B SE 436894B SE 8005122 A SE8005122 A SE 8005122A SE 8005122 A SE8005122 A SE 8005122A SE 436894 B SE436894 B SE 436894B
- Authority
- SE
- Sweden
- Prior art keywords
- acid
- gpt
- alanine
- substrates
- activities
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 18
- 102000003929 Transaminases Human genes 0.000 title claims description 10
- 108090000340 Transaminases Proteins 0.000 title claims description 10
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 claims description 18
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 14
- ADVPTQAUNPRNPO-UHFFFAOYSA-N 2-azaniumyl-3-sulfinopropanoate Chemical compound OC(=O)C(N)CS(O)=O ADVPTQAUNPRNPO-UHFFFAOYSA-N 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 12
- ADVPTQAUNPRNPO-REOHCLBHSA-N 3-sulfino-L-alanine Chemical compound OC(=O)[C@@H](N)C[S@@](O)=O ADVPTQAUNPRNPO-REOHCLBHSA-N 0.000 claims description 10
- 239000000758 substrate Substances 0.000 claims description 10
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 9
- 229960003767 alanine Drugs 0.000 claims description 9
- 229940107700 pyruvic acid Drugs 0.000 claims description 9
- 101710088194 Dehydrogenase Proteins 0.000 claims description 7
- 235000014655 lactic acid Nutrition 0.000 claims description 7
- 239000004310 lactic acid Substances 0.000 claims description 7
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims description 6
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims description 6
- 230000001575 pathological effect Effects 0.000 claims description 5
- 229940024606 amino acid Drugs 0.000 claims description 4
- 235000001014 amino acid Nutrition 0.000 claims description 4
- 150000001413 amino acids Chemical class 0.000 claims description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 6
- 235000006408 oxalic acid Nutrition 0.000 claims 2
- 108010020056 Hydrogenase Proteins 0.000 claims 1
- 239000012429 reaction media Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 11
- KHPXUQMNIQBQEV-UHFFFAOYSA-N oxaloacetic acid Chemical compound OC(=O)CC(=O)C(O)=O KHPXUQMNIQBQEV-UHFFFAOYSA-N 0.000 description 6
- 210000002966 serum Anatomy 0.000 description 6
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000008033 biological extinction Effects 0.000 description 4
- 229950006238 nadide Drugs 0.000 description 4
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 4
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 3
- BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 description 3
- 235000004279 alanine Nutrition 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000005891 transamination reaction Methods 0.000 description 3
- 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 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 238000004737 colorimetric analysis Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000010405 reoxidation reaction Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- WRWGAMITZOWMJJ-UHFFFAOYSA-N 2-hydroxypropanoic acid 2-oxopropanoic acid Chemical compound C(C(=O)C)(=O)O.C(C(=O)C)(=O)O.C(C(O)C)(=O)O WRWGAMITZOWMJJ-UHFFFAOYSA-N 0.000 description 1
- VXUGVISSBXKUEL-UHFFFAOYSA-N 2-hydroxypropanoic acid;2-oxopropanoic acid Chemical compound CC(O)C(O)=O.CC(=O)C(O)=O VXUGVISSBXKUEL-UHFFFAOYSA-N 0.000 description 1
- MMKXZVZBTQSEMU-UHFFFAOYSA-N 2-oxo-3-sulfinylpropanoic acid Chemical compound OC(=O)C(=O)C=S=O MMKXZVZBTQSEMU-UHFFFAOYSA-N 0.000 description 1
- 206010023126 Jaundice Diseases 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 241000269319 Squalius cephalus Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- HWXBTNAVRSUOJR-UHFFFAOYSA-N alpha-hydroxyglutaric acid Natural products OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 description 1
- 229940009533 alpha-ketoglutaric acid Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 239000006225 natural substrate Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- -1 phenyl hydrazone Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007430 reference method Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- 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
- C12Q1/48—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase
- C12Q1/52—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase involving transaminase
-
- 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
- Y10S435/81—Packaged device or kit
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Immunology (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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT49789/79A IT1162349B (it) | 1979-07-17 | 1979-07-17 | Metodo per la determinazione delle transaminasi e relativo kit diagnostico |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8005122L SE8005122L (sv) | 1981-01-18 |
| SE436894B true SE436894B (sv) | 1985-01-28 |
Family
ID=11271566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8005122A SE436894B (sv) | 1979-07-17 | 1980-07-11 | Sett att samtidigt bestemma transaminaser (got och gpt) med kinetisk uv-metod |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4329425A (OSRAM) |
| JP (1) | JPS5935600B2 (OSRAM) |
| AR (1) | AR224900A1 (OSRAM) |
| AT (1) | AT369034B (OSRAM) |
| AU (1) | AU528558B2 (OSRAM) |
| BE (1) | BE884323A (OSRAM) |
| CA (1) | CA1144459A (OSRAM) |
| CH (1) | CH647600A5 (OSRAM) |
| DE (1) | DE3026854C2 (OSRAM) |
| ES (1) | ES493473A0 (OSRAM) |
| FR (1) | FR2461952A1 (OSRAM) |
| IL (1) | IL60504A (OSRAM) |
| IT (1) | IT1162349B (OSRAM) |
| NL (1) | NL8004080A (OSRAM) |
| SE (1) | SE436894B (OSRAM) |
| ZA (1) | ZA804096B (OSRAM) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1171257B (it) * | 1981-05-28 | 1987-06-10 | Biodata Spa | Metodo per la determinazione della attivita' degli isoenzimi citoplasmatico e mitocondriale della glutammico ossalacetico transaminasi nel siero o plasma umano |
| DE3221730A1 (de) * | 1982-06-09 | 1983-12-15 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und analytische mittel zur aktivitaetsbestimmung von glutamat-oxalacetat-transaminase |
| DE3330246A1 (de) * | 1983-08-22 | 1985-03-14 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und reagenz zur bestimmung von transaminasen |
| US4547460A (en) * | 1984-04-16 | 1985-10-15 | Eastman Kodak Company | Multizone analytical element and method for analyte determination |
| US5834226A (en) * | 1991-01-31 | 1998-11-10 | Xytronyx, Inc. | One-step test for aspartate aminotransferase |
| JPH05900U (ja) * | 1991-06-19 | 1993-01-08 | 株式会社新来島どつく | 折り畳み式梯子 |
| JPH0693713A (ja) * | 1992-09-14 | 1994-04-05 | Kashiwabara Token Kogyo Kk | 円筒タンクの外壁面作業用足場 |
| KR100318552B1 (ko) * | 1998-12-24 | 2002-09-05 | 한국과학기술연구원 | 간질환관련표식물질의검출용스트립 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3206376A (en) * | 1964-05-22 | 1965-09-14 | Warner Lambert Pharmaceutical | Method of determining glutamic-oxalacetic transaminase |
| US3746625A (en) * | 1966-12-12 | 1973-07-17 | H Bergmeyer | Stabilized coenzyme test compositions |
| BE786291A (fr) * | 1971-07-20 | 1973-01-15 | Technicon Instr | Compositions de diagnostic pour determination de la glutamate-oxalate-transaminase (got) et de la glutamate-pyruvate-transaminase (gpt) |
| JPS5631957B2 (OSRAM) * | 1973-10-09 | 1981-07-24 | ||
| US4241179A (en) * | 1978-08-14 | 1980-12-23 | Coulter Electronics, Inc. | Method for determining a transaminase in a biological fluid and reagent combination for use in the method |
-
1979
- 1979-07-17 IT IT49789/79A patent/IT1162349B/it active
-
1980
- 1980-07-04 IL IL60504A patent/IL60504A/xx not_active IP Right Cessation
- 1980-07-07 CA CA000355611A patent/CA1144459A/en not_active Expired
- 1980-07-08 ZA ZA00804096A patent/ZA804096B/xx unknown
- 1980-07-10 US US06/168,286 patent/US4329425A/en not_active Expired - Lifetime
- 1980-07-11 SE SE8005122A patent/SE436894B/sv not_active IP Right Cessation
- 1980-07-15 AR AR281764A patent/AR224900A1/es active
- 1980-07-15 AU AU60407/80A patent/AU528558B2/en not_active Ceased
- 1980-07-15 BE BE0/201416A patent/BE884323A/fr unknown
- 1980-07-16 AT AT0370280A patent/AT369034B/de not_active IP Right Cessation
- 1980-07-16 CH CH5459/80A patent/CH647600A5/it not_active IP Right Cessation
- 1980-07-16 NL NL8004080A patent/NL8004080A/nl not_active Application Discontinuation
- 1980-07-16 JP JP55096297A patent/JPS5935600B2/ja not_active Expired
- 1980-07-16 DE DE3026854A patent/DE3026854C2/de not_active Expired
- 1980-07-17 ES ES493473A patent/ES493473A0/es active Granted
- 1980-07-17 FR FR8015815A patent/FR2461952A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2461952A1 (fr) | 1981-02-06 |
| AR224900A1 (es) | 1982-01-29 |
| BE884323A (fr) | 1980-11-03 |
| CH647600A5 (it) | 1985-01-31 |
| JPS5655200A (en) | 1981-05-15 |
| ATA370280A (de) | 1982-04-15 |
| ES8106556A1 (es) | 1981-09-01 |
| IT7949789A0 (it) | 1979-07-17 |
| US4329425A (en) | 1982-05-11 |
| AT369034B (de) | 1982-11-25 |
| DE3026854C2 (de) | 1986-09-18 |
| AU528558B2 (en) | 1983-05-05 |
| IL60504A (en) | 1983-07-31 |
| ES493473A0 (es) | 1981-09-01 |
| FR2461952B1 (OSRAM) | 1983-08-05 |
| IL60504A0 (en) | 1980-09-16 |
| NL8004080A (nl) | 1981-01-20 |
| IT1162349B (it) | 1987-03-25 |
| JPS5935600B2 (ja) | 1984-08-29 |
| AU6040780A (en) | 1981-01-22 |
| SE8005122L (sv) | 1981-01-18 |
| CA1144459A (en) | 1983-04-12 |
| ZA804096B (en) | 1981-08-26 |
| DE3026854A1 (de) | 1981-02-12 |
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