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Calibration-Free Quantitative Analysis of mRNA

机译:mRNA的无标定定量分析

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摘要

Here we introduce a method for accurate and sensitive quantitative analysis of mRNA, which does not require calibration with mRNA. The method uses a fluorescently labeled hybridization probe as a reference standard. It involves the following: (i) annealing mRNA to the excess of the fluorescently labeled ssDNA hybridization probe, (ii) separation of the mRNA-probe hybrid from the excess of the probe by gel-free capillary electrophoresis mediated by ssDNA-binding protein, (iii) fluorescence detection of the hybrid and the excess probe, and (iv) quantification of mRNA using a simple algebraic formula. The method also overcomes a number of other limitations of conventional methods: the entire procedure currently takes only 2 h and accurately quantifies 10~(5) copies of mRNA. With further improvements to the method, the procedure can be potentially shortened to 10 min, and the limit of quantification can be decreased to as few as 100 copies of mRNA. In this work, we prove the principle of the method by quantifying mRNA of green fluorescent protein in the matrix of total cellular RNA. The developed method is quantitative, simple, fast, and highly sensitive. It requires commercially available instrumentation only. The method will be an indispensable tool for molecular and cell biology studies.
机译:在这里,我们介绍了一种无需进行mRNA校准即可对mRNA进行准确而灵敏的定量分析的方法。该方法使用荧光标记的杂交探针作为参考标准。它涉及以下方面:(i)将mRNA退火至过量的荧光标记ssDNA杂交探针,(ii)通过ssDNA结合蛋白介导的无凝胶毛细管电泳将mRNA-探针杂交与过量的探针分离, (iii)杂交体和过量探针的荧光检测,以及(iv)使用简单的代数公式对mRNA进行定量。该方法还克服了常规方法的许多其他局限性:整个过程目前仅需2 h即可准确定量mRNA的10〜(5)个拷贝。通过对该方法的进一步改进,可以将程序潜在地缩短到10分钟,并且定量限可以减少到100个拷贝的mRNA。在这项工作中,我们通过定量总细胞RNA基质中绿色荧光蛋白的mRNA证明了该方法的原理。所开发的方法定量,简单,快速且高度灵敏。它仅需要市售仪器。该方法将是进行分子和细胞生物学研究必不可少的工具。

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