1、

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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2、
3、

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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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。

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5、

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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7、

This is the website of the Restriction Enzyme Database.

这是限制酶数据库的网站。

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8、

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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9、

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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10、

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。

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11、

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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12、

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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13、

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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14、

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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15、

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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16、

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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17、

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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18、

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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19、

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.

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20、

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.

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