1)  RNase P
核酶 RNase P
2)  RNase P
RNase P
1.
Targeted in vitro Cleavage of Human Cytomegalovirus UL54 mRNA Segments by RNase P;
RNase P核酶对人巨细胞病毒UL54基因mRNA体外切割作用
2.
RNase P was a ribonucleoprotein complex, which was responsible for the 5 maturation of precurosor tRNAs, and abroad existed in Archaebacteria, bacterium, yeast and animals.
RNase P是一种核蛋白复合物，广泛存在于古细菌、细菌、酵母和动物体内，它可以特异性地剪切tRNA前体(ptRNA)的5’末端，形成成熟的tRNA。
3)  RNase P ribozyme
RNase P Ribozyme
4)  RNase P
核酶P
1.
Methods:The M1GS-T6 ribozyme was constructed by linking the catalytic RNA subunit of RNase P from Escherichia coli(M1 RNA) covalently to a guide sequence(GS) that is complementary to the mRNA coding sequence of UL97,which encode a phosphotransferase of HCMV.
方法:针对HCMV UL97 mRNA T6位点设计与之互补的引导序列(Guide Sequence,GS),将其共价结合至大肠杆菌核酶P催化亚基(M1 RNA)的3′末端,构建M1GS-T6核酶,并用其对UL97基因亚克隆片段转录产物进行体外靶向切割实验。
2.
Methods Using the pFL117 plasmid,which containing M1 gene of the RNase P from Escherichia coli as the template,DNA products encoding the artificial M1GS gene which contain different lengths of bridge sequences were amplified with PCR method.
方法以含大肠杆菌核酶P催化单位(M1 RNA)基因的pFL117质粒作为模板,通过巧妙设计不同的下游引物,经PCR扩增、扩增产物克隆及克隆基因的体外转录,构建一组具有不同桥序列的人工M1GS核酶。
3.
Objective:To explore the cleaved ability of RNase P target HCMV UL97 mRNA in vitro.
目的　探讨核酶P对HCMVUL97mRNA的体外切割能力。
5)  Ribonuclease P (RNase P)
核酶P（RNaseP）
6)  RNase P RNA gene
RNase P RNA基因
参考词条
补充资料：酒化酶、醇酶、发酵酶
分子式：
CAS号：

性质：又称酒化酶、醇酶、发酵酶。从酵母中分离而得的一系列酶。不耐热。它能催化酒精发酵反应，与糖酵解有关，如磷酸化酶、醛缩酶、葡萄糖磷酸变位酶、葡萄糖6-磷酸酶等。

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