restriction enzyme

It enables a specific gene to be located on a particular restriction enzyme fragment.

它就能使专一的基因被定位于特定的限制性内切酶切成的片段上。

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

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

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

The recombined clone was confirmed by restriction enzyme and sequencing analysis.

将获得基因片段重组到pCI质粒中，转化到大肠杆菌Top10后挑选克隆，利用限制性酶切和核苷酸序列分析鉴定重组质粒。

The Restriction Enzyme Database from NEB.

限制苺资料库取自新英格兰生物实验室公司.

Restriction Enzyme Mediated Integration, a New Strategy for Cloning New Genes

限制酶介导整合技术：一种克隆新基因的新策略

Gene mappings were made in 11 cases among 25 immuno-positives with restriction enzyme.

从25例中随机抽取11例作限制性内切酶解的基因图谱分析，以对照检查酶联免疫吸附试验法的准确度，结果10例为α-地贫1，基因型是αα/一一；

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。

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

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。

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

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

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。

Studies on restriction enzyme map of mitochondrial DNA from Silurus asotus

鲇鱼线粒体DNA的酶切图谱

The restriction digestion system consisted of 10μ L PCR products, 2.0μ L 10× Buffer, 83.350 nkat restriction enzyme and 7.5μ L ddH 2 O.

PCR产物10.0μL, 加入2.0μL10×Buffer, 83.350nkat内切酶,7.5μL双蒸水构成20μL酶 切反应体系.

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。

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。

This is the website of the Restriction Enzyme Database.

这是限制酶数据库的网站。

Ultrasensitive detection method for restriction enzyme cleavage product using molecular beacon.

建立了限制性内切酶切割产物的超灵敏检测方法。

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。

Results The expressive vector has been constructed and confirmed by restriction enzyme digestion and DNA sequencing analysis.

结果构建的表达载体经过限制性内切酶分析和DNA序列测定，证实准确无误。

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

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。

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。

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。

Restriction Enzyme Map Of Human IFN-α_1 Gene

人α1型干扰素基因的酶切图谱

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。

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。

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。