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不同人源性细胞中内参基因的筛选

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目的 为筛选在不同人源性细胞中能够稳定表达的内参基因,以期为不同组织的定量研究提供一定的参考。方法 通过实时荧光定量PCR(RT-qPCR)方法检测36种人源性细胞中β-珠蛋白(β-Globin)、甘油醛-3-磷酸脱氢酶(GAPDH)、核糖体RNA(18S rRNA)和核糖核酸酶P(Rnase P)4个候选内参基因的表达量,并利用geNorm、NormFider和BestKeeper三个软件对候选内参基因的稳定性进行评价。结果 同一种细胞中,Rnase P的表达量较高;不同细胞中,18SrRNA的表达较为稳定。结论 综合分析发现候选内参基因18S rRNA虽较为稳定,但并不是最优选择。
Screening of reference genes in different human-derived cells
[Objective]To screen internal reference genes that can be stably expressed in different human-derived cells,in order to provide a certain reference for quantitative research of different tissues.[Methods]The Expression of β-Globin,GAPDH,18S rRNA and Rnase P four candidate reference genes in 36 types of human-derived cells was detected by real-time fluorescence quantitative PCR(RT-qPCR).The stability of four candidate reference genes was evaluated using geNorm,NormFider and BestKeeper software.[Results]In the same type of cell,the expression of Rnase P is relatively high;in different cells,the expression of 18S rRNA is relatively stable.[Conclusion]Comprehensive analysis found that although the candidate reference gene 18S rRNA is relatively stable,it is not the best choice.

human-derived cellsreference genesscreen

李俊慧、裴倩倩、赵晓转、王新明、刘功成

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郑州标源生物与科技有限公司研发部,河南郑州 450016

人源性细胞 内参基因 筛选

2024

中国医学工程
中国医药生物技术协会 卫生部肝胆肠外科研究中心

中国医学工程

影响因子:0.504
ISSN:1672-2019
年,卷(期):2024.32(6)