用两种不同方法分离 RNA,分析小鼠脂肪组织的脂肪生物标志物

D. Chu, Hue Vu Thi, Ngoc Hoan Le
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引用次数: 0

摘要

RNeasy Mini Kit 和 TRI Reagent 协议是提取总 RNA 的常用技术,在有关脂肪生物标志物表达的研究中被广泛使用。本研究旨在建立和确定从冷冻脂肪组织中分离 RNA 的适当方法,目的是分析脂肪生物标志物。研究人员使用 RNeasy Mini Kit 和 TRI Reagent 方法从冷冻的小鼠白色脂肪组织(-80oC)中提取总 RNA。使用 NanoDrop 对 RNA 的浓度和纯度进行了评估。采用一步式 RT-qPCR 对三种脂肪生物标志物的 mRNA 表达水平进行量化:MEST、SFRP5 和 SCD1。研究结果表明,与 TRI 试剂法相比,RNeasy Mini 试剂盒产生的 RNA 浓度更高。此外,RNeasy Mini 试剂盒提供的 RNA 样品纯度更高,260/230 比率也更高。虽然使用 TRI 试剂提取的 RNA 在三种生物标志物的 mRNA 表达水平上略有升高,但这些差异未达到统计学意义。总之,两种方法都适用于总 RNA 提取,但建议使用 RNeasy Mini 试剂盒来获得更高的 RNA 浓度和纯度。选择哪种方法应根据 RNA 的下游应用而定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA isolation by two different methods in analysing adipose-biomarkers of mouse adipose tissues
The RNeasy Mini Kit and the TRI Reagent protocol are commonly employed techniques for extracting total RNA and are widely utilised in research pertaining to the expression of adipose biomarkers. This study was undertaken to establish and determine an appropriate method for isolating RNA from frozen adipose tissue, with the objective of analysing adipose biomarkers. Total RNA was extracted from frozen white adipose tissues of mice (-80oC) using both the RNeasy Mini Kit and the TRI Reagent protocol. The concentration and purity of the RNA were assessed using NanoDrop. One-step RT-qPCR was employed to quantify the mRNA expression levels of three adipose biomarkers: MEST, SFRP5, and SCD1. The results of this investigation indicated that the RNeasy Mini Kit yielded a higher RNA concentration when compared to the TRI Reagent method. Furthermore, the RNeasy Mini Kit provided RNA samples with superior purity, as evidenced by a higher 260/230 ratio. Although RNA extracted using the TRI Reagent exhibited slightly elevated mRNA expression levels for the three biomarkers, these differences did not reach statistical significance. In summary, both methods are suitable for total RNA extraction, but the RNeasy Mini Kit is recommended for obtaining higher RNA concentration and purity. The choice of method should be contingent upon the intended downstream application of the RNA.
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