The Determination of Human Urinary [gamma]-Esterase Activity using Antibody-Conjugated Paper Disk
A new and specific method for the determination of human urinary γ-esterase activity, which migrates to the γ-globulin region on cellulose acetate electrophoresis, was developed using an antibody-conjugated paper disk. The method was applied experimentally, and the results indicate that an increase...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1982-08, Vol.30 (8), p.2870 |
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creator | IIIZUMI, YUICHI ADACHI, TETSUO ITO, YOSHIMASA HIRANO, KAZUYUKI SUGIURA, MAMORU SAWAKI, SHUNJI MORIKAWA, MASAKO INOUE, MICHIKO TSUBOI, MINORU |
description | A new and specific method for the determination of human urinary γ-esterase activity, which migrates to the γ-globulin region on cellulose acetate electrophoresis, was developed using an antibody-conjugated paper disk. The method was applied experimentally, and the results indicate that an increase of γ-esterase activity in the urine reflects renal damage, that is, urinary γ-esterase activity was increased in patients with nephrotic syndrome (20.3±15.0 units/g of creatinine) and chronic nephritis (8.00±5.23 units/g of creatinine) as compared with that of healthy subjects (3.08±1.90 units/g of creatinine). γ-Esterase was localized at the renal tubules of a patient with renal disease, and it was considered that γ-esterase was excreted in the urine when the renal tubules were damaged. Therefore, the determination of urinary γ-esterase activity by this method should be an effective aid in the diagnosis of renal disease. |
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The method was applied experimentally, and the results indicate that an increase of γ-esterase activity in the urine reflects renal damage, that is, urinary γ-esterase activity was increased in patients with nephrotic syndrome (20.3±15.0 units/g of creatinine) and chronic nephritis (8.00±5.23 units/g of creatinine) as compared with that of healthy subjects (3.08±1.90 units/g of creatinine). γ-Esterase was localized at the renal tubules of a patient with renal disease, and it was considered that γ-esterase was excreted in the urine when the renal tubules were damaged. 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The method was applied experimentally, and the results indicate that an increase of γ-esterase activity in the urine reflects renal damage, that is, urinary γ-esterase activity was increased in patients with nephrotic syndrome (20.3±15.0 units/g of creatinine) and chronic nephritis (8.00±5.23 units/g of creatinine) as compared with that of healthy subjects (3.08±1.90 units/g of creatinine). γ-Esterase was localized at the renal tubules of a patient with renal disease, and it was considered that γ-esterase was excreted in the urine when the renal tubules were damaged. 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The method was applied experimentally, and the results indicate that an increase of γ-esterase activity in the urine reflects renal damage, that is, urinary γ-esterase activity was increased in patients with nephrotic syndrome (20.3±15.0 units/g of creatinine) and chronic nephritis (8.00±5.23 units/g of creatinine) as compared with that of healthy subjects (3.08±1.90 units/g of creatinine). γ-Esterase was localized at the renal tubules of a patient with renal disease, and it was considered that γ-esterase was excreted in the urine when the renal tubules were damaged. Therefore, the determination of urinary γ-esterase activity by this method should be an effective aid in the diagnosis of renal disease.</abstract><cop>Tokyo</cop><pub>Japan Science and Technology Agency</pub></addata></record> |
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title | The Determination of Human Urinary [gamma]-Esterase Activity using Antibody-Conjugated Paper Disk |
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