JPH0229319B2 - - Google Patents
Info
- Publication number
- JPH0229319B2 JPH0229319B2 JP56196302A JP19630281A JPH0229319B2 JP H0229319 B2 JPH0229319 B2 JP H0229319B2 JP 56196302 A JP56196302 A JP 56196302A JP 19630281 A JP19630281 A JP 19630281A JP H0229319 B2 JPH0229319 B2 JP H0229319B2
- Authority
- JP
- Japan
- Prior art keywords
- plasmin
- lysyl
- lower alkyl
- alkyl group
- leucyl
- 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 - Lifetime
Links
- 229940012957 plasmin Drugs 0.000 claims description 51
- 108010088842 Fibrinolysin Proteins 0.000 claims description 49
- 239000000758 substrate Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
- 239000002806 plasmin inhibitor Substances 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 150000001412 amines Chemical class 0.000 claims description 18
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 16
- 229940122791 Plasmin inhibitor Drugs 0.000 claims description 14
- 239000003153 chemical reaction reagent Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 10
- 239000003593 chromogenic compound Substances 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 239000012491 analyte Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 238000003556 assay Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 24
- 210000002381 plasma Anatomy 0.000 description 16
- 239000012895 dilution Substances 0.000 description 13
- 238000010790 dilution Methods 0.000 description 13
- 238000005259 measurement Methods 0.000 description 13
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000007853 buffer solution Substances 0.000 description 7
- 239000000872 buffer Substances 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 5
- 239000012089 stop solution Substances 0.000 description 5
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 5
- 239000007983 Tris buffer Substances 0.000 description 4
- 239000005018 casein Substances 0.000 description 4
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical group 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 description 4
- 235000021240 caseins Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 3
- 238000011088 calibration curve Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000012264 purified product Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 206010005133 Bleeding tendencies Diseases 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 230000020764 fibrinolysis Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000002489 hematologic effect Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
Landscapes
- Investigating Or Analysing Biological Materials (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19630281A JPS5898097A (ja) | 1981-12-08 | 1981-12-08 | α↓2−プラスミンインヒビタ−の測定法及び測定用試薬 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19630281A JPS5898097A (ja) | 1981-12-08 | 1981-12-08 | α↓2−プラスミンインヒビタ−の測定法及び測定用試薬 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5898097A JPS5898097A (ja) | 1983-06-10 |
JPH0229319B2 true JPH0229319B2 (fr) | 1990-06-28 |
Family
ID=16355541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19630281A Granted JPS5898097A (ja) | 1981-12-08 | 1981-12-08 | α↓2−プラスミンインヒビタ−の測定法及び測定用試薬 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5898097A (fr) |
-
1981
- 1981-12-08 JP JP19630281A patent/JPS5898097A/ja active Granted
Non-Patent Citations (1)
Title |
---|
BIOCHIM BIOPHYS ACTA=1968 * |
Also Published As
Publication number | Publication date |
---|---|
JPS5898097A (ja) | 1983-06-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Rick | Trypsin | |
US4578361A (en) | Creatinine antibody | |
JP2955345B2 (ja) | リムラス変形細胞溶解産物および発色原基質を用いたエンドトキシン反応速度論的アッセイ | |
JPH06258326A (ja) | エンドトキシン特異的測定剤 | |
JP4427137B2 (ja) | フルクトシルバリンの生産方法 | |
US3769173A (en) | Determination of gamma-glutamyl transpeptidase in biological fluids | |
JP2005512547A5 (fr) | ||
US5073487A (en) | Rapid assay for functional human α1 -proteinase inhibitor | |
IE55677B1 (en) | Iodothyronine immunoassays employing hms as tbp blocking agent | |
JPH0236239B2 (fr) | ||
US5175089A (en) | Method for monitoring periodontal disease by monitoring endotoxins and inflammatory agents | |
JPH0229319B2 (fr) | ||
DK164512B (da) | Fremgangsmaade til simultan bestemmelse af prokallikrein og den partielle thromboplastintid | |
JPS62220199A (ja) | 体液の試料中の総−ビリルビンの測定のための方法および試薬 | |
Trautschold et al. | Kallikrein | |
JPH0687795B2 (ja) | マクロ分子ヒドロラ−ゼ用螢光偏光アツセイ、このアツセイに使用する試薬及びこれら試薬の製法 | |
JPH0248239B2 (fr) | ||
Kirchhof et al. | Control of anticoagulant therapy with a chromogenic substrate | |
US4778755A (en) | Immunoassay method | |
EP0085402B1 (fr) | Méthode de détermination du kallikreine dans l'urine humaine et trousse d'essai à cette fin | |
Bing et al. | Inactivation of the first component of human complement by m-[o-(2-chloro-5-fluorosulfonylphenylureido) phenoxybutoxy] benzamidine | |
Uete et al. | A fluorometric assay of the acetylcholinesterase activity in blood | |
JPS5847491A (ja) | β−D−ガラクトシダ−ゼ作用の停止方法 | |
JPS62180269A (ja) | 遊離型サイロキシンの酵素免疫測定法 | |
JP2001281253A (ja) | 酵素免疫測定法による試料中の測定対象物質の測定試薬及び測定方法 |