首页> 外国专利> method of determination of alkaline phosphatase activity in biological fluids

method of determination of alkaline phosphatase activity in biological fluids

机译:液体中碱性磷酸酶活性的测定方法

摘要

the invention belongs to the field of medicine, namely to clinical laboratory diagnosis, and can be used to determine the activity of alkaline phosphate u0437u044b in biological fluidsin particular, in saliva.the essence of the invention is a reagent to the sample receiving the biological fluid.spend u0438u043du043au0443u0431u0430u0446u0438u044e obtained mixture with cocktail and determine the concentration of the protein after incubation by measuring the optical density of the mixture on the x u043eu043bu043eu0441u0442u043eu0439 samples and subsequent calculationwith the receipt of the original mixture as a biological fluid using saliva, and reagent prepared by mixing buffer solution u0434u0438u044du0442u0430u043du043eu043b amin 1 mmol / ml with magnesium with 0.5 u043cu043au043cu043eu043bu044c / ml and an r - u043du0438u0442u0440u043eu0444u0435u043du0438u043bu0444u043eu0441u0444u0430u0442u0430 5 u043cu043au043cu043eu043bu044c / ml followed by 1 ml to obtain a mixture to u0440u0435u0430u0433u0435u043du0442u0443 add 100 mkl samples of biological fluidsafter stirring the obtained mixture u0438u043du043au0443u0431u0430u0446u0438u044e are within 5 min at a temperature 37u00b0u0441, add in 1 ml of solution of sodium u0433u0438u0434u0440u043eu043eu043au0438u0441u0438 05 mol / l (20 g / l) and mix with subsequent measurement of optical density against a single sample with the wavelength of 405 nm in a ditch with a layer thick 10 mm during the time jeni to 30 minutesand the activity of alkaline phosphatase in the e / l count using the importance factor, calculated as the ratio of total solution in the ditch to the coefficient u043cu0438u043bu043bu0438u043cu043e used as p - u043du0438u0442u0440u043eu0444u0435u043du043eu043bu0430 1875 and the volume of biological fluid sample, the sample is in the form of a mixture u0445u043eu043bu043eu0441u0442u0443u044e reagent with distilled water in the same numbers as the original u0441u043cu0435u0441 and, thewith the above same operations as the original mixture.
机译:本发明属于医学领域,即属于临床实验室诊断,可用于测定生物流体特别是唾液中碱性磷酸酶的活性。本发明的实质是一种用于接收样品的试剂花费 u0438 u043d u043a u0443 u0431 u0430 u0446 u0438 u044e将混合物与鸡尾酒混合,孵育后,通过测量x上混合物的光密度来确定蛋白质的浓度。 u043b u043e u0441 u0442 u043e u0439样品并随后计算,并使用唾液接收原始混合物作为生物流体,并通过混合缓冲溶液 u0434 u0438 u044d u0442 u0430 u043d u043e u043b amin 1 mmol / ml与镁和0.5 u043c u043a u043c u043e u043b u044c / ml和r- u043d u0438 u0442 u0440 u043e u0444 u0435 u043d u043d u0438 u043b u0444 u043e u0441 u0444 u0430 u0442 u0430 5 u043c u043a u043c u043e u043b u044c / ml,然后加1 ml,得到的混合物在搅拌得到的混合物后,加入100 mkl的生物液体样品。 u0440 u0435 u0430 u0433 u0435 u043d u0442 u0443 u0446 u0438 u044e在5分钟内,温度为37 u00b0 u0441,加入1毫升钠溶液 u0433 u0438 u0434 u0440 u043e u043e u043a u0438 u0441 u0438 05 mol / l(20 g / l),然后与在波长为405 nm的单个样品中的光密度测量相混合,并在30分钟的时间间隔内,在厚度为10 mm的一个沟中,并测量碱性磷酸酶的活性。 e / l使用重要性因子计数,计算为沟渠中总溶液与系数 u043c u0438 u043b u043b u043b u0438 u043c u043e的比率,用作p- u043d u0438 u0442 u0440 u875e u0444 u0435 u043d u043e u043b u04b u0430 1875和生物流体样品的体积,样品的混合物形式为 u0445 u043e u043b u043e u0441 u0442 u0443 u044e重新装填用蒸馏水以与原始混合物相同的数量进行蒸馏,并具有与原始混合物相同的操作。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号