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限制性酶切分析，限制性内切酶分析
1、effector enzyme───效应酶
2、restriction orifice───节流孔板
3、enzyme───n.[生化]酶
4、assimilatory enzyme───同化酶
5、restriction enzyme───[遗]限制性内切酶；[遗]限制酶
6、analysis───n.分析；分解；验定
7、conjugated enzyme───缀合酶；结合酶类；[生化]结合酶
8、restriction───n.限制；约束；束缚
9、caloric restriction───[医]热限制
1、sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.───CR检测和酶切鉴定结果表明，在水平测试的混合饲料粉中可检出牛源、羊源性成分。
2、Finally a recombinant plasmid named pcNcSRS2, which was identified by PCR, restriction enzyme analysis and sequencing, was obtained.───经PCR鉴定、限制性内切酶分析和克隆片段序列测定、比较，证实了重组质粒的正确性。
3、were prepared by alkali lysis and purified with polyethylene glycol 8000. Restriction enzyme analysis show that both genes are well-constructed suitable for transgenic animal experiment.───限制性酶切图谱分析证实这两个基因的结构是完整的，符合转基因实验要求。
4、Results The three results of restriction enzyme analysis are coincident completely, and the method is more precise than RT-PCR.───结果限制性内切酶分析法的三次检测结果完全一致，较RT-PCR法的检测结果更精确。
5、Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.───结果酶切和测序证实PTEN基因克隆和真核表达载体构建成功。
6、Polymerase chain reaction and restriction enzyme analysis of human cytomegalovirus infection in pregnant women and neonates───孕妇及新生儿巨细胞病毒感染的聚合酶链反应及限制酶分析
1、Methods: The serum samples were collected from 56 patients with morbilliform maculopapular eruption. The target DNA of CBV was detected by RT-PCR and restriction enzyme analysis.
2、Subcloning and comparative restriction enzyme analysis were carried out with the replication origin from tne integrated F' plasmid and that from the autonomous F plasmid.
3、Plasmid DNAs were prepared by alkali lysis and purified with polyethylene glycol 8000. Restriction enzyme analysis show that both genes are well-constructed suitable for transgenic animal experiment.
4、The recombinant plasmid pcDNA3 F was stable within the host stain ZJ111 in vitro and in vivo as shown by restriction enzyme analysis and PCR identification of the F gene.
5、Finally a recombinant plasmid named pcNcSRS2, which was identified by PCR, restriction enzyme analysis and sequencing, was obtained.
6、The bovine, sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.
7、Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.