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首页> 外文期刊>Electronic Journal of Biotechnology >Improved isolation of good-quality total RNA from the optic stalk of Mud crab, Scylla paramamosain
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Improved isolation of good-quality total RNA from the optic stalk of Mud crab, Scylla paramamosain

机译:改进了从泥蟹视神经Sc的视杆中分离高质量总RNA的方法

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An improved and efficient protocol was developed based on the TaKaRa RNAiso Plus Kit (Code: D9108A) for isolating good-quality total RNA from the optic stalk of mud crab, Scylla paramamosain. The protocol was based on the Trizol method with modifications. The carapace overlapping the optic stalk was retained with RNA in regular protocol. In order to remove the abundant deposition correlative with the carapace which makes the isolation of RNA particularly difficult, 5M potassium acetate solution (pH = 6.0) was added before the precipitation of RNA, and the temperature of RNA deposition was also decreased to -70oC to ensure the stabilization of RNA. Good-quality total RNA from the optic stalk of S. paramamosain could be easily isolated with this modified protocol and three conventional methods were also employed to confirm the quality of RNA. This improved method would be helpful in facilitating molecular research of crabs involving RNA from the optic stalk.
机译:基于TaKaRa RNAiso Plus试剂盒(代码:D9108A),开发了一种改进的高效协议,用于从泥蟹视神经Sc(Scyla paramamosain)的视柄中分离出高质量的总RNA。该协议基于带有修饰的Trizol方法。重叠视杆的甲壳按常规方法用RNA保留。为了去除与甲壳相关的大量沉积,这使得分离RNA特别困难,在RNA沉淀之前添加5M乙酸钾溶液(pH = 6.0),并将RNA的沉积温度降至-70oC。确保RNA的稳定。用这种改进的方案可以很容易地分离出副链霉菌视杆中的高质量总RNA,并且还采用了三种常规方法来确认RNA的质量。这种改进的方法将有助于促进蟹蟹涉及视杆RNA的分子研究。

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