首页> 外国专利> METHOD FOR SIMULTANEOUS DNA TESTING TO DETECT PRESENCE OF H63D AND C282Y POLYMORPHISMS IN HFE GENE ASSOCIATED WITH GENETIC HEMACHROMATOSIS

METHOD FOR SIMULTANEOUS DNA TESTING TO DETECT PRESENCE OF H63D AND C282Y POLYMORPHISMS IN HFE GENE ASSOCIATED WITH GENETIC HEMACHROMATOSIS

机译:同时进行DNA检测的HFE基因中H63D和C282Y多态性与遗传性血液病相关的方法

摘要

FIELD: molecular biology, medicine.;SUBSTANCE: disclosed is improved method for simultaneous genetic typing of H63D and C282Y polymorphisms in HFE gene by using PCR method in real time with fluorescent detection. Claimed method includes a) step of reaction mixture containing no analyzed DNA preincubation at +4°C for at least 1 hour; b) application of "hot start" method to activate reaction and c) selection of optimal pairs of fluorescent dye/quenching agent, namely FAM and BHQ1 for normal variant 63H probe; R6G and BHQ1 for mutant variant 63D probe; ROX and BHQ2 for normal variant 282C probe; and Cy5 and BHQ3 for mutant variant 282Y probe. Claimed method is fully adapted to clinical application.;EFFECT: method with high specificity level.;10 dwg, 2 tbl 3 ex
机译:领域:公开了一种改进的方法,其通过使用荧光检测的实时PCR方法同时对HFE基因中的H63D和C282Y多态性进行基因分型。所要求保护的方法包括:a)在+ 4℃下至少1小时不包含经分析的DNA预温育的反应混合物的步骤; b)应用“热启动”方法来激活反应,以及c)选择最佳的荧光染料/猝灭剂对,即正常63H探针的FAM和BHQ1。 R6G和BHQ1用于突变体63D探针;正常变体282C探头的ROX和BHQ2;突变变体282Y探针的Cy5和BHQ3。要求的方法完全适合临床应用。效果:高特异性水平的方法; 10 dwg,2 tbl 3 ex

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