Tackett Michael R, Diwan Izzuddin
Abcam Inc., One Kendall Square Suite, B2304, Cambridge, MA, 02139, USA.
Methods Mol Biol. 2017;1654:209-219. doi: 10.1007/978-1-4939-7231-9_14.
Accuracy of miRNA profiling is enhanced when sample processing can be kept to a minimum, avoiding steps such as RNA purification that can introduce bias and inaccuracies. Here we describe a novel multiplex circulating miRNA assay that enables the profiling of up to 65 miRNAs of choice in the same well directly from plasma (including heparin plasma) or serum, with no need for RNA purification. The main component of the assay is FirePlex™ hydrogel particles, which enable the multiplex capture of miRNAs with picomolar sensitivity and high specificity. Results are obtained using conventional flow cytometry and easy to use software, which allows fast analysis and interpretation of the experimental data. This chapter provides methods to profile miRNAs with PCR sensitivity from as little as 10 μL of crude biofluid sample, or from less than 100 pg of purified RNA.
当样本处理能保持在最低限度,避免诸如RNA纯化等可能引入偏差和不准确的步骤时,miRNA分析的准确性会得到提高。在此,我们描述了一种新型的多重循环miRNA检测方法,该方法能够直接从血浆(包括肝素血浆)或血清中在同一孔中对多达65种选定的miRNA进行分析,而无需进行RNA纯化。该检测方法的主要成分是FirePlex™水凝胶颗粒,它能够以皮摩尔灵敏度和高特异性对miRNA进行多重捕获。使用传统流式细胞术和易于使用的软件获得结果,该软件允许对实验数据进行快速分析和解读。本章提供了从低至10 μL的粗生物流体样本或少于100 pg的纯化RNA中以PCR灵敏度分析miRNA的方法。