首页> 外国专利> WAY EXPRESS assess the degree of aneuploidy BASED ON NUCLEAR morphometry peripheral blood lymphocytes of human, cultured under conditions cytokinetic UNIT, IN identify potential genotoxic activity SUBSTANCES AND ENVIRONMENTAL FACTORS

WAY EXPRESS assess the degree of aneuploidy BASED ON NUCLEAR morphometry peripheral blood lymphocytes of human, cultured under conditions cytokinetic UNIT, IN identify potential genotoxic activity SUBSTANCES AND ENVIRONMENTAL FACTORS

机译:WAY EXPRESS基于细胞核动力学条件下培养的人类核细胞形态学评估外周血淋巴细胞的非整倍性程度,以确定潜在的遗传毒性活性物质和环境因素

摘要

FIELD: medicine.;SUBSTANCE: invention refers to medicine, namely cytogenetics and may be used for instant assessment of a degree of potential genotoxic substance activity and environmental factors by the presence of aneuploidy in human peripheral blood lymphocytes formed by culture in cytogenetic block. That is ensured by culture of human blood lymphocytes in cytogenetic block in the presence of an analysed substance. Cells are fixed. Cytogenetic preparations are prepared and stained. Images of 100 cells containing two separate nuclei and having no visible, including genetic injures are recorded after staining for each preparation with the use of an optical microscope with an integrated digital camera at magnification 10×40. These images are used to derive a sum and a relation of nuclei areas in each such cell. The derived values are used for calculating medians, upper and lower quartiles, their relation and difference. The preparations are statically compared by these parameters. If considerable differences are found at a significance level of p≤0.05, as well as a dose response is observed, ability for the analysed substance to induce aneuploidy associated with potential genotoxic activity is stated.;EFFECT: invention provides reducing time and simplifying procedure of assessing a degree of aneuploidy in the analysis system of genotoxic activity of factors of any nature.;7 dwg, 2 ex
机译:技术领域本发明涉及医学,即细胞遗传学,并且可用于通过在细胞遗传学阻断物中培养形成的人外周血淋巴细胞中存在非整倍性来立即评估潜在的遗传毒性物质活性和环境因素的程度。在存在被分析物质的情况下,通过在细胞遗传学模块中培养人血淋巴细胞来确保这一点。单元格是固定的。制备细胞遗传学制剂并染色。每种制剂染色后,使用光学显微镜和集成数码相机以10×40的放大倍数记录100个细胞的图像,该细胞包含两个独立的细胞核并且不可见,包括遗传损伤。这些图像用于导出每个此类单元格中的核面积之和和关系。导出的值用于计算中位数,上下四分位数,它们之间的关系和差异。通过这些参数对制剂进行静态比较。如果在p≤0.05的显着性水平上发现相当大的差异,并且观察到剂量响应,则表明所分析的物质诱导与潜在的遗传毒性活性相关的非整倍性的能力。评估任何性质的因子的遗传毒性活性分析系统中的非整倍性程度; 7 dwg,2 ex

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