首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Chemiluminescence detection of telomere DNA in human cells on a membrane by using fluorescein-5-isothiocyanate-labeled primers
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Chemiluminescence detection of telomere DNA in human cells on a membrane by using fluorescein-5-isothiocyanate-labeled primers

机译:使用荧光素5-异硫氰酸酯标记的引物化学发光检测膜上人细胞中的端粒DNA

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Telomere DNA is related to cell aging and cancer genesis because the telomeric region of DNA sequences at chromosome ends are shortened with cell divisions. Therefore, a sensitive and specific detection method is required for the telomere DNA. Here we propose a chemiluminescence (CL)-based method for the sensitive detection of telomere DNA in human cells. In this study, the telomere DNA was amplified by polymerase chain reaction (PCR) using special forward and reverse primers labeled with fluorescein-5-isothiocyanate (FITC) at the 5′ end, and then the FITC-containing PCR products were detected by CL reaction with 3,4,5-trimethoxyphenylglyoxal (TMPG) after electrophoresis followed by Southern blot onto a nylon membrane. The TMPG reagent specifically reacted with guanine moiety in DNA at room temperature and provided CL intensities. The CL intensities from the PCR products could be enhanced approximately 10-fold using FITC-labeled primers as compared with those using nonlabeled primers. The detection limit of the PCR products with the proposed method was 0.3 ng on the membrane. The developed CL method could quantitatively determine the telomere DNA in a small number of human cells (~350) and gave approximately 10 times higher sensitivity than a conventional fluorescence-based method.
机译:端粒DNA与细胞衰老和癌症的发生有关,因为染色体末端的DNA序列的端粒区会随着细胞分裂而缩短。因此,端粒DNA需要灵敏且特异性的检测方法。在这里,我们提出了一种基于化学发光(CL)的方法,用于敏感检测人细胞中的端粒DNA。在这项研究中,端粒DNA通过聚合酶链反应(PCR)使用5'末端标记有荧光素5-异硫氰酸酯(FITC)的特殊正向和反向引物进行扩增,然后通过CL检测含有FITC的PCR产物电泳后与3,4,5-三甲氧基苯基乙二醛(TMPG)反应,然后在尼龙膜上进行Southern印迹。 TMPG试剂在室温下与DNA中的鸟嘌呤部分特异性反应并提供CL强度。与未标记引物相比,使用FITC标记引物可将PCR产物的CL强度提高约10倍。所提出的方法在膜上的PCR产物的检出限为0.3 ng。发达的CL方法可以定量测定少量人细胞(〜350个)中的端粒DNA,其灵敏度比传统的基于荧光的方法高约10倍。

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