Peynot Nathalie, Duranthon Véronique, Khan Daulat Raheem
UMR1198 Biologie du Développement et Reproduction, INRA, Jouy-en-Josas, 78350, France.
Methods Mol Biol. 2015;1222:181-96. doi: 10.1007/978-1-4939-1594-1_14.
Real-time, reverse transcription quantitative PCR (RT-qPCR) is a highly sensitive and reproducible technology for the analysis of gene expression patterns. Its ability to detect minute quantities of nucleic acid from multifarious sources makes it an ideal technique for embryonic transcript quantification. However, complex cellular diversity and active transcriptome dynamics in early embryos necessitate particular caution to avoid erroneous results. This chapter is intended to outline basic methodology to design and execute RT-qPCR experiments in pre-implantation embryos.
实时逆转录定量PCR(RT-qPCR)是一种用于分析基因表达模式的高度灵敏且可重复的技术。它能够检测来自多种来源的微量核酸,这使其成为胚胎转录本定量的理想技术。然而,早期胚胎中复杂的细胞多样性和活跃的转录组动态变化需要特别谨慎,以避免产生错误结果。本章旨在概述在植入前胚胎中设计和执行RT-qPCR实验的基本方法。