首页> 外国专利> Analysis method and reagent kit for the quantitative in vitro determination in biological specimens of the activity of proteins that cause multidrug resistance in tumors.

Analysis method and reagent kit for the quantitative in vitro determination in biological specimens of the activity of proteins that cause multidrug resistance in tumors.

机译:分析方法和试剂盒,用于在生物样本中定量测定引起肿瘤多药耐药性的蛋白质活性。

摘要

HERE ARE describes a method DIAGNOSTIC TEST KITS FOR DETERMINING QUANTITATIVE REAGENT IN VITRO ACTIVITY IN BIOLOGICAL SPECIMENS CAUSING PROTEIN MDR multidrug resistance in tumors. THE METHOD OF THE INVENTION IS BASED ON THE MEASUREMENT OF SPEED COMPOUND accumulation in cells of the specimen (advantageously by fluorescence measurement); This compound is not a good protein substrate MDR PRESENT IN THE SAMPLE NO pervious CELL AND BEING FORMED IN CELLS, by generally present in cells ENZYMES, FROM A compound which is a good substrate of said protein MDR pervious CELL AND IN VITRO the specimen is added. Based on the method of the invention it is possible to calculate a factor value MDR activity (MAF) IS IN THE RANGE OF RELEVANT DIAGNOSIS, CHARACTERISTIC OF ACTIVITY MDR, THAT IS, THE LEVEL OF RESISTANCE multidrug OF SPECIMEN .
机译:这里描述了一种诊断测试盒的方法,该测试盒用于确定生物样品中引起蛋白质MDR多药耐药性的生物样品中的定量活性。本发明的方法基于对标本细胞中速度化合物积聚的测量(有利地通过荧光测量)。该化合物不是存在于样品中的良好的蛋白质底物MDR,通常不存在于渗透细胞中,并通常在细胞中存在,通常存在于细胞酶中,该化合物是该蛋白质MDR的良好底物,并且是体外添加的。基于本发明的方法,可以计算出因子值MDR活性(MAF)在相关诊断的范围内,活性MDR的特征即抗药性的多药水平。

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