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Expression Stabilities of Ten Candidate Reference Genes for RT-qPCR in Zanthoxylum bungeanum Maxim

Real-time reverse transcription quantitative PCR has become a common method for studying gene expression, however, the optimal selection of stable reference genes is a prerequisite for obtaining accurate quantification of transcript abundance. Suitable reference genes for RT-qPCR have not yet been i...

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Detalles Bibliográficos
Autores principales:	Fei, Xitong, Shi, Qianqian, Yang, Tuxi, Fei, Zhaoxue, Wei, Anzhi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2018
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017173/ https://www.ncbi.nlm.nih.gov/pubmed/29601541 http://dx.doi.org/10.3390/molecules23040802

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