The genotypes of apoE, apoC-I and LRP genes were analyzed by using PCR and restriction fragment length polymorphism ( RFLP) techniques.

Analyze the differences in the genes expressions of the two types of the cells using restriction fragment difference display method.

使用限制性酶切片段差异展示技术分离滑膜成纤维细胞与皮肤成纤维细胞差异表达之基因。

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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。

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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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