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首页> 外文期刊>Turkish journal of zoology >Validation of reference genes for quantitative expression analysis by qPCR in various tissues of date mussel ( Lithophaga lithophaga )
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Validation of reference genes for quantitative expression analysis by qPCR in various tissues of date mussel ( Lithophaga lithophaga )

机译:QPCR在日期贻贝各种组织中验证参考基因的定量表达分析(LITHOPHAGA LITHOPHAGA)

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qPCR is a very popular method for identifying nucleotide sequences as a result of its sensitivity and relatively low cost and technical simplicity. Normalization is one of the most important steps in analyzing qPCR data and the use of reference genes is the most common normalization strategy. In the present study five commonly used reference genes ( 18S, 28S, ef1a, ?-act , and ?-tub ) were evaluated for their stability in the mantle, gill, foot, and pallial gland of date mussel ( L. lithophaga ) in different seasons. Four different software packages were used for evaluation: geNorm, NormFinder, BestKeeper, and RefFinder. Although these programs contain different algorithms and analytical procedures, their ranking of the candidate reference genes was similar. Of the five selected reference genes 18S, 28S , and ef1a were determined as the three most stable in different tissues and seasons. A-tub was evaluated as the least stable reference gene and therefore inappropriate for normalization of quantitative gene expression data. The results will help improve the accuracy of gene expression analysis in samples of date mussel and at the same time provide guidance for selection of reference genes in future qPCR studies in the species.
机译:QPCR是一种非常流行的方法,用于鉴定其敏感性和相对较低的成本和技术简单的结果。归一化是分析QPCR数据的最重要步骤之一,参考基因的使用是最常见的标准化策略。在本研究中,在贻贝(L.Leithophaga)的披风,鳃,脚和痛风中,评估五种常用的参考基因(18秒,28s,Ef1a,α-,和Δ-tub)。不同的季节。四种不同的软件包用于评估:Genorm,Normfinder,Bestkeeper和Reffinder。虽然这些程序包含不同的算法和分析程序,但它们的候选参考基因的排名相似。在五种选定的参考基因18s,28s和Ef1a中被确定为不同组织和季节中最稳定的三个。评估A桶作为最低稳定的参考基因,因此不适合定量基因表达数据的标准化。结果将有助于提高日期贻贝样品中基因表达分析的准确性,同时为各种QPCR研究中选择参考基因的选择提供指导。

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