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首页> 外文期刊>Nucleosides, nucleotides and nucleic acids >Determination of ITPase activity in erythrocyte lysates obtained for determination of TPMT activity.
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Determination of ITPase activity in erythrocyte lysates obtained for determination of TPMT activity.

机译:测定用于确定TPMT活性的红细胞裂解物中的ITPase活性。

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摘要

The indication for the determination of both thiopurine methyltransferase (TPMT) and inosine triphosphate pyrophosphohydrolase is identical (i.e., adverse drug reactions toward mercaptopurines). Therefore, we tested whether or not our standard procedure to prepare erythrocyte lysates for measurement of TPMT activity, which includes treatment with Chelex 100 (a chelating resin), was suitable for the measurement of ITPase activity. It also was tested to see if ITPase activity differs in EDTA and Heparin anti-coagulated blood samples. We found that there was no difference between the ITPase activity in erythrocyte lysates prepared from EDTA or Heparin anti-coagulated blood. Treatment with a chelating resin or omission of magnesium from the assay procedure resulted in decreased and nearly absent ITPase activity, respectively. We conclude that untreated erythrocyte lysates obtained for determination of TPMT activity are suitable for determination of ITPase activity. However, after treatment with Chelex 100 the erythrocyte lysates become unsuitable for determination of ITPase activity.
机译:同时测定硫嘌呤甲基转移酶(TPMT)和肌苷三磷酸焦磷酸水解酶的适应症是相同的(即,对巯基尿嘧啶的不良药物反应)。因此,我们测试了制备用于测量TPMT活性的红细胞裂解液的标准程序(包括用Chelex 100(一种螯合树脂)进行的处理)是否适合于测量ITPase活性。还测试了EDTA和肝素抗凝血样中ITPase活性是否不同。我们发现在由EDTA或肝素抗凝血液制备的红细胞裂解物中,ITPase活性之间没有差异。用螯合树脂处理或从测定程序中遗漏镁分别导致ITPase活性降低和几乎缺失。我们得出结论,为确定TPMT活性而获得的未经处理的红细胞裂解物适用于确定ITPase活性。然而,在用Chelex 100处理后,红细胞裂解物变得不适合确定ITPase活性。

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