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通过微流控平台对牛生殖系统样本进行真实的基因表达分析。

Bona fide gene expression analysis of samples from the bovine reproductive system by microfluidic platform.

机构信息

Laboratory of Phytomedicines, Pharmacology and Biotechnology, Department of Pharmacology, Institute of Biosciences, University of São Paulo State (Unesp), Campus of Botucatu, São Paulo, Brazil.

Laboratory of Phytomedicines, Pharmacology and Biotechnology, Department of Pharmacology, Institute of Biosciences, University of São Paulo State (Unesp), Campus of Botucatu, São Paulo, Brazil; University of Western São Paulo (Unoeste), Campus of Presidente Prudente, São Paulo, Brazil.

出版信息

Anal Biochem. 2020 May 1;596:113641. doi: 10.1016/j.ab.2020.113641. Epub 2020 Feb 20.

Abstract

Sample types such as those from reproductive systems often yield scarce material, which limits RT-qPCR analysis to only a few targets. Recently developed high-throughput systems can potentially change this scenario, however, the nanoliter scale of such platforms requires extra processing, e.g., preamplification, which needs to be defined through observation and experience. In order to establish best practices in high-throughput PCR approaches using samples from reproductive systems, we evaluated the Biomark™ HD performance using 11 different sample types from the bovine reproductive system: blastocyst (single/pool), oocyte (pool), cumulus, granulosa, and theca cells, oviduct tissue, fetal ovary, testicle (adult/fetal), and uterine horn. We observed that the preamplification step is not just reliable, but mandatory. Our results indicated that 14-preamplification cycles associated to 5- and 7-fold-dilution is the best approach for those samples. Additionally, the Biomark™ HD system has a high intra and inter reproducibility, therefore its performance in duplicate is unnecessary for the ΔCq analysis, taking in consideration the cutoff value 4 < Cq < 22. In summary, this high-throughput approach is a reliable and excellent tool for studying the bovine reproductive system, especially using quantitatively-limited samples, as a larger number of target genes can be assessed from a very low amount of starting material.

摘要

样本类型,如生殖系统的样本,通常产生的材料很少,这限制了 RT-qPCR 分析只能针对少数几个目标。最近开发的高通量系统可能会改变这种情况,然而,这种平台的纳升级规模需要额外的处理,例如预扩增,这需要通过观察和经验来定义。为了在使用生殖系统样本的高通量 PCR 方法中建立最佳实践,我们使用牛生殖系统的 11 种不同样本类型评估了 Biomark™ HD 性能:囊胚(单个/混合)、卵母细胞(混合)、卵丘、颗粒细胞和膜细胞、输卵管组织、胎儿卵巢、睾丸(成年/胎儿)和子宫角。我们观察到预扩增步骤不仅可靠,而且是必需的。我们的结果表明,对于这些样本,14 个预扩增循环与 5 倍和 7 倍稀释相结合是最佳方法。此外,Biomark™ HD 系统具有很高的内和间重现性,因此在考虑到 4 < Cq < 22 的截止值时,其在重复分析中的性能对于 ΔCq 分析是不必要的。总之,这种高通量方法是研究牛生殖系统的可靠且出色的工具,特别是在使用定量有限的样本时,可以从非常少量的起始材料中评估更多数量的靶基因。

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