小鼠脑源性内皮细胞总rna的提取及逆转录。猪链球菌感染2例

Mingcheng Liu, O. Kasianenko
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引用次数: 1

摘要

猪链球菌2型是一种重要的新型人畜共患病原体。它主要引起猪的脑膜炎。我们用SS2感染bEnd。3 .获得稳定的cDNA,为下一步细胞因子基因表达和蛋白表达差异的研究提供依据。本文介绍了针对bEnd的SS2研究。3感染获得稳定的cDNA,用于后续研究基因表达差异和细胞因子蛋白表达差异。目的:从猪链球菌血清2型(SS2)感染的小鼠脑源性内皮细胞(bEnd.3)中提取总RNA并转录成互补DNA (cDNA)。材料与方法:SS2菌株来源于吉林大学。弯曲。3名来自中国河南科技学院。逆转录试剂盒来自日本Takara公司。Trizol来自中国Bioteke公司。Nanodrop仪器来自美国Thermo公司。聚合酶链反应(PCR)仪来自德国Biometra公司。我们使用SS2感染bEnd。3 .感染倍数(MOI)为100,持续12h。收集细胞,采用Trizol法提取bEnd总RNA。3个被SS2感染。采用纳米滴法测定RNA浓度及OD260/280、OD260/230值。用PCR仪逆转录试剂盒将RNA转录为cDNA。结果:本研究采用的三唑法可靠,获得了高质量的RNA。通过反转录试剂盒获得稳定的cDNA。结论:本实验获得了高质量的RNA,并逆转录为稳定的cDNA,可用于后续相关细胞因子的检测。本研究为下游研究提供了一种近似的RNA提取方法和良好的实验基础。
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Extraction and reverse transcription of total rna from mouse brain-derived endothelial cells.3 infected by streptococcus Suis 2
Streptococcus suis 2 is an important emerging zoonotic pathogen. It mainly causes meningitis in pigs. We use SS2 to infect bEnd.3 to get stable cDNA for next research on differences in gene expression and protein expression of cytokines. The paper presents an SS2 study for bEnd.3 infection to obtain stable cDNA for subsequent study of differences in gene expression and cytokine protein expression. Objective: The aim of this study was to extract the total RNA from mouse brain-derived Endothelial cells (bEnd.3) infected by Streptococcus suis serotype 2 (SS2) and transcript to complementary DNA (cDNA). Materials and methods: SS2 strain were obtained from Jilin University, China. BEnd.3 was from Henan institute of Science of Technology, China. Reverse transcription kit was from Takara company, Japan. Trizol was from Bioteke company,China. Nanodrop instrument was from Thermo company, USA. Polymerase chain reaction (PCR) instrument was from Biometra company, Germany. We used SS2 to infect bEnd.3 at a multiplicity of infection (MOI) of 100 for 12h. Cells were harvested and Trizol method was chose to extract the total RNA of bEnd.3 infected by SS2. Nanodrop instrument was used to measure the concentration of RNA and the values of OD260/280 and OD260/230. RNA were transcripted to cDNA with reverse transcription kit by PCR instrument. Results: trizol method used in this study was reliable and high-quality RNA were obtained. Stable cDNA were obtained by reverse transcription kit. Conclusion: in this experiment high-quality RNA was obtained and reverse transcribed to stable cDNA for subsequent detection of related cytokines. This study provides an approximate RNA extraction method and good experimental foundation for downstream research.
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