Shen Feng
SlipChip Corporation, 230 Constitution Drive, Menlo Park, CA, 94025, USA.
Methods Mol Biol. 2017;1547:123-132. doi: 10.1007/978-1-4939-6734-6_10.
Digital nucleic acid amplification (Digital NAA) quantifies nucleic acid by compartmentalizing a sample of DNA or RNA into a large number of discrete partitions and performing parallel nucleic acid amplification, such as polymerase chain reaction (PCR) or isothermal amplification reactions. With the counts of positive wells, total number of wells, and volumes of wells, the concentration of the target nucleic acid in the sample can be quantified. Digital NAA is considered increasingly powerful for ultra-sensitive detection and accurate quantification of nucleic acid for biological research and potentially medical diagnostics. Here, we describe glass SlipChip devices to perform digital NAA without cumbersome manual manipulation or complex fluidic control systems.
数字核酸扩增(Digital NAA)通过将DNA或RNA样本分隔到大量离散分区中并进行平行核酸扩增,如聚合酶链反应(PCR)或等温扩增反应,来对核酸进行定量。通过阳性孔的计数、孔的总数以及孔的体积,可以对样本中目标核酸的浓度进行定量。数字核酸扩增对于生物研究和潜在的医学诊断中核酸的超灵敏检测和准确定量而言,被认为越来越强大。在此,我们描述了玻璃滑片芯片设备,以在无需繁琐手动操作或复杂流体控制系统的情况下进行数字核酸扩增。