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METHOD FOR GENETIC POLYMORPHISM RAPID ANALYSIS FOR DETECTION OF GENETIC PREDISPOSITION TO BREAST CANCER

机译:遗传多态性快速分析方法检测乳腺癌的遗传易感性

摘要

FIELD: biotechnology.;SUBSTANCE: method is for rapid analysis of genetic polymorphism to detect genetic predisposition to breast cancer (BC). 40 bases long oligonucleotides containing the genetic marker and not containing the genetic marker shown in Table 1, are immobilized on the microchip, 3 repetitions of each oligonucleotide, together with those shown in Table 3 from human housekeeping gene as a positive control and from genes of other organisms that have no homology in the human genome, as a negative control. Nucleic acids are selected from the blood sample, using the total RNA or DNA. A labeled probe is obtained for hybridization by reverse transcription reaction with simultaneous fluorescent labeling for RNA or nick translation labeling of DNA. The obtained probe is hybridized with oligonucleotides immobilized on the microchip. The non-specifically bound probe is washed under conditions discriminating against mutant genotypes. The microchip is scanned and the results evaluated.;EFFECT: increased specificity and reliability of the analysis and improved breast cancer risk assessment reliability.;3 tbl, 1 dwg
机译:领域:生物技术;研究对象:该方法用于快速分析遗传多态性,以检测乳腺癌的遗传易感性。将40个碱基长的包含遗传标记但不包含表1所示遗传标记的寡核苷酸固定在微芯片上,每种寡核苷酸与表3所示的寡核苷酸一起重复3次重复,这些重复来自人看家基因作为阳性对照以及在人类基因组中没有同源性的其他生物,作为阴性对照。使用总RNA或DNA从血液样本中选择核酸。通过逆转录反应,同时进行RNA的荧光标记或DNA的缺口翻译标记,获得了用于杂交的标记探针。将获得的探针与固定在微芯片上的寡核苷酸杂交。非特异性结合的探针在区别突变基因型的条件下洗涤。扫描微芯片并评估结果。效果:增加分析的特异性和可靠性,并提高乳腺癌风险评估的可靠性。3 tbl,1 dwg

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