1·This is the website of the Restriction Enzyme Database.
这是限制酶数据库的网站。
2·Restriction enzyme site analysis was used to confirm the mutation.
突变位点经限制性内切酶分析证实。
3·Note: Underline sequences are cleavage sites of restriction enzyme.
注：标有下划线的碱基序列为限制酶切位点。
4·The recombinants were analyzed and identified by restriction enzyme, PCR and sequencing.
通过酶切、PCR及测序鉴定各重组体。
5·Both genes were correctly cloned and identified by PCR, restriction enzyme digestion and sequencing.
经pcr鉴定、酶切鉴定和测序说明所克隆的两种基因是正确的。
6·The length and the results of restriction enzyme digestion indicate that the amplified products are respected.
各扩增产物长度和限制性酶酶切结果表明均为预期产物。
7·Based on the number of restriction enzyme detecting RFLPs, most of mutations were attributed to point mutation.
根据揭示多态性的限制性内切酶的数量可将产生的突变大多归为点突变。
8·Results The constructed vectors of EBO-WT and EBO-G87 were identified by restriction enzyme digestion and nucleotide sequencing.
结果构建的EBO G87和EBO WT重组载体经内切酶双酶切鉴定及核苷酸序列测定证实。
9·The bovine, sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.
P 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。
10·Restriction enzyme: Protein (more specifically, an endonuclease) produced by bacteria that cleaves DNA at specific sites along its length.
限制性内切：由细菌产生的一种蛋白质，能在特定的地方切断去氧核糖核酸分子。收藏。