Modified Assay Method for Placental Alkaline Phosphatase:The Method of Electrophoresis and Heat Treatment
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概要
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<BR>1. A method was developed for the separative assay of placental alkaline phosphatase in human serum from the isozymes derived from other organs using acetate membrane electrophoresis with an electrophoresis buffer containing 2×10<SUP>-3</SUP>M of MgCl<SUB>2</SUB>.<BR>2. the activity of placental alkaline phosphatase was completely recovered after the electrophoresis for 40 minutes by the addition of 2×10<SUP>-3</SUP>M of MgCl<SUB>2</SUB> to the electrophoresis buffer and to the applied serum.<BR>3. It was possible to measure accurately the placental alkaline phosphatase activity between l and 30 K-AU. using this method.<BR>4. Neale1) described that placental alkaline phosphatase activity could be determined by treating serum a 56° for 30 minutes. But it is difficalt to obtain the constant results, because it is essential to adjust the temperature accurately at 56°<BR>5. Placental alkaline phosphatase actMty in sera could be correctly determined only when the samples were heated at 56-58° for 30 minutes after the treatment with 10<SUP>-3</SUP>M of EDTA and 3×10<SUP>-3</SUP>M of MgCl<SUB>2</SUB> at 37° for 20 minutes.
著者
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勝沼 恒彦
東海大学医学部生化学
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藤井 成彬
東海大学産婦人科
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田村 公子
東海大学共同利用研究所生化学部
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林 茂一郎
東海大学産婦人科
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小林 一夫
東海大学産婦人科
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勝沼 恒彦
東海大学医学部・生化学
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