The length and the results of restriction enzyme digestion indicate that the amplified products are respected.

Restriction Enzyme Map Of Human IFN-α_1 Gene

人α1型干扰素基因的酶切图谱

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The DNA vaccine was identified by restriction enzyme analysis, sequencing and expression.

对此疫苗进行酶切、测序和表达鉴定。

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The mutation was confirmed by digestion of the PCR products with restriction enzyme.

发现突变后用特异性限制性内切酶对突变位点进行酶切，验证突变。

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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

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Restriction enzyme analysis of human papilloma virus ( hpv) dna from common warts

人乳头瘤病毒DNA的限制性核酸内切酶分析

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Restriction enzyme mapping and SDS-PAGE protein analysis were done on four transformants.

还进行了限制酶酶切分析和蛋白质SDS-PAGE分析。

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The construct was confirmed by PCR, restriction enzyme digestion and direct sequencing.

经限制性内切酶酶切和测序证实。

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Rapid Preparation and Restriction Enzyme Analysis of the DNA of Canine Adenovirus Type 2

犬Ⅱ型腺病毒DNA的快速提取及限制性酶切分析

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To verified the by restriction enzyme digestion, bacterial colony PCR, and sequencing analysis.

并对重组质粒进行双酶切、菌落PCR及测序分析进行鉴定。

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This is the website of the Restriction Enzyme Database.

这是限制酶数据库的网站。

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And the results were further confirmed by restriction enzyme analysis of the genomic DNA fragments.

限制性酶切分析其基因组DNA。

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Restriction enzyme pattern analysis of the DNAs of three nuclear polyhedrosis viruses

三种昆虫核型多角体病毒DNA的限制性内切酶酶解分析

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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。

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The target fragment was digested by restriction enzyme to determine the accuracy of the detection technology.

用限制性内切酶酶切的方法判断该检测技术的准确性。

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And have been identified by PCR and restriction enzyme digestion successfully constructed recombinant viruses.

并经过PCR和酶切鉴定重组病毒构建成功。

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Identification of 12 Mycobacteria to the Species Level by Polymerase Chain Reaction and Restriction Enzyme Analysis

采用PCR法和限制性内切酶分析对12种分枝杆菌进行鉴定

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Recombinants were confirmed by colony PCR and restriction enzyme digestion.

经菌落PCR和质粒酶切鉴定后，将目的基因进行序列测定。

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REMI transformation efficiency was 19.12~ 22.72 times higher than normal plasmid transformation without restriction enzyme.

实验结果还表明，REMI的转化效率是一般质粒转化效率的19.12～22.72倍。

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In vitro Enlargement of pBR322 and the Related Restriction Enzyme Maps

质粒pBR322的体外扩建以及有关限制性核酸内切酶图谱

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Restriction Enzyme Analysis and Molecular Cloning of CAV-1 DNA

犬Ⅰ型腺病毒DNA的酶切分析及分子克隆

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