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首页> 外文期刊>Molecular biotechnology >An improved protocol for the isolation of RNA from roots of tea (Camellia sinensis (L.) O. Kuntze)
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An improved protocol for the isolation of RNA from roots of tea (Camellia sinensis (L.) O. Kuntze)

机译:一种从茶树根中提取RNA的改进方案(山茶)

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Tea, a beverage crop, is a rich source of polyphenols and polysaccharides which greatly attribute to its importance. However, oxidation and precipitation of these compounds during nucleic acids extraction is a limitation to molecular biology and genomic studies. On isolation of total RNA from root tissue using established protocols, difficulties were encountered in terms of purity and quantity of isolated RNA or some of the methods were time-consuming and also yields were low. The present communication combines a phenol-based RNA isolation protocol with a cetyltrimethylammonium bromide-based procedure with appropriate modifications. This protocol successfully isolated RNA from tap root tissue in 2-3 h as compared with 16 h reported by the previous method. Also, RNA yield was higher by more than fourfold. The RNA isolated by this protocol was successfully used for downstream applications such as RT-PCR and the construction of suppression subtractive hybridization library. The developed protocol worked well with other plant tissue with high polyphenols and polysaccharides contents.
机译:茶作为一种饮料作物,是多酚和多糖的丰富来源,这很大程度上归功于其重要性。然而,在核酸提取期间这些化合物的氧化和沉淀是分子生物学和基因组研究的限制。使用已建立的方案从根组织中分离总RNA时,在分离RNA的纯度和数量方面遇到了困难,或者某些方法耗时且产量也很低。本通讯将基于苯酚的RNA分离方案与基于十六烷基三甲基溴化铵的程序进行了适当的修改。与先前方法报道的16小时相比,该协议在2-3小时内成功地从水龙头根组织中分离了RNA。同样,RNA产量提高了四倍以上。通过该方案分离的RNA已成功用于下游应用,例如RT-PCR和构建抑制消减杂交文库。所开发的协议可与其他具有高多酚和多糖含量的植物组织很好地配合使用。

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