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Comparison of the Efficiency of Different Methods for the Lysis of Cells in Lab-on-Chip Systems

机译:芯片实验室系统中细胞裂解的不同方法的效率比较

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摘要

Quantitative or qualitative examination of DNA has enormous impact on medical, forensic, or genealogical, analysis. The macro as well as micro world knows a panel of different methods for cell lysis that has to happen prior to the purification of the DNA. To our knowledge the efficiency of those protocols as well as the purity/amplifiability of extracted DNA has not been compared for a Lab-on-a-Chip application so far. To address this issue, human HeLa cells were lysed on-chip by chemical, enzymatic, thermal or mechanical treatment, or by application of strong pH gradients. These tests are currently complemented by approaches using exposure to strong electrical fields, ultrasonic treatment or radio frequencies. In the first instance quantity and purity of DNA was inspected by agarose gel electrophore-sis. Up to now, the chemical lysis by applying Guanidinium SCN and the electrochemical lysis represent to be the best DNA isolation protocols in our chip-based test system.
机译:DNA的定量或定性检查对医学,法医或家谱分析具有巨大影响。宏世界和微观世界都知道在纯化DNA之前必须进行的一系列细胞裂解方法。据我们所知,到目前为止,尚未将这些方案的效率以及提取的DNA的纯度/可扩增性用于芯片实验室应用。为了解决这个问题,通过化学,酶促,热处理或机械处理,或通过施加强pH梯度,将人HeLa细胞裂解在芯片上。这些测试目前通过使用暴露于强电场,超声处理或射频的方法进行补充。首先,通过琼脂糖凝胶电泳检查DNA的数量和纯度。到目前为止,在我们基于芯片的测试系统中,应用胍盐SCN进行化学裂解和电化学裂解代表了最佳的DNA分离方案。

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