1) Ribonuclease P (RNase P)
核酶P(RNaseP)
2) RNase P
RNaseP
1.
To research technique for gene silence and antiviral agents, ribozyme M1GS-T6 was constructed from external guide sequences(EGSs)that consist of a sequence complementary to HCMV UL54 gene RNA and M1 RNA, the catalytic RNA subunit of RNase P from Escherichia coli.
为研究病毒基因沉默工具和抗病毒制剂,以人巨细胞病毒UL54基因mRNA序列设计互补的外部引导序列,共价结合到大肠杆菌来源RNaseP催化核心M1RNA上,从而构建成M1GS-T6核酶。
2.
tRNase Z,RNase P and tRNA splicing endonuclease are three major endonucleases that participate in pre-tRNA processing.
tRNaseZ、RNaseP和tRNA剪接内切酶是参与tRNA前体加工的三种主要的核酸内切酶,分别参与tRNA前体3'末端、tRNA前体5'末端和内含子剪接的加工。
3) RNase P
核酶P
1.
DNA-EGS1386 in cells induced RNase P inhibits the expression of human cytomegalovirus UL49 gene
DNA-EGS1386胞内诱导核酶P抑制人巨细胞病毒UL49基因的表达
2.
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。
3.
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。
4) RNase P
核糖核酸酶P
5) RNase P(M1-RNA)
核糖核酸酶P(M1-RNA)
6) human ribonuclease P
人类核糖核酸酶P
1.
Research advance on human ribonuclease P;
人类核糖核酸酶P的研究进展
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。
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。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条