1、

Screening Genes Related to Piglet ETEC F4 Receptor with δ DDRT-PCR Method

δ差异显示法筛选仔猪ETEC F4受体相关基因

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2、

The P1 structure gene was amplified by PCR method.

采用PCR扩增方法获取P1结构基因。

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3、

Analysis of PCR-RFLP on LPL Gene of Six Chicken Breeds

6个品种鸡LPL基因的PCR-RFLP分析

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4、

Objective : To establish fluorescence quantitative nested RT-PCR method for detecting Borna disease virus ( BDV ).

目的: 建立博尔纳病病毒 ( BDV ) 荧光定量套式RT -PCR 检测方法,为快速、准确地定量检测BDV奠定基础.

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5、

D 13 S 317 locus was sequencing by Beckman CEQ 8800. The PCR products were analyzed by PAG vertical electrophoresis.

用BeckmanCEQ 8800毛细管测序仪测定序列, 应用PCR技术和聚丙烯酰胺凝胶垂直板电泳分型.

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6、

After PCR and sequencing, the expression plasmid pWD κ H was transfected into CHO ( dhfr ~-) cells.

经PCR和测序鉴定正确后, 用lipofectAMINE2 000转染CHO ( dhfr - ) 细胞.

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7、

The full length CMO cDNA was cloned from Salicornia europaea by RT-PCR and RLM-RACE.

本研究利用RT -PCR 和RLM-RACE技术获得了盐角草的CMOcDNA全序列.

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8、

To review PCR-based genotyping methods for genetic polymorphism of CYP 2 A 6 gene.

综述检测CYP2A6基因多态性的PCR技术的基因型方法.

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9、

RT-PCR kit was obtained from Takara Company.

RT-PCR试剂盒为hkaa产品,引物均由北京奥科公司合成。

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10、

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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11、

Cathepsin E , Maspin, S 100 P was analyzed with immunohistochemical analysis , PCR , ELISA, Western blotting in the specimens obtained by EUS-FNA.

免疫印迹法检测胰腺癌EUS-FNA 活检物中CathepsinE 、 Maspin 、 S100P蛋白含量.

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12、

Methods The tlh gene amplified by PCR was cloned into the vector pET32a+ and sequenced, followed by analysis of the biological information by with presenting the sequences to the websites of bioinformatics on the Internet.

方法利用PCR技术扩增tlh基因,克隆至载体pET32a+并测序。将测序结果提交国际互联网上有关生物信息网站进行生物信息学分析。

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13、

Thrombopoietin ( TPO) cDNA obtained by RT-PCR from human fetal liver

利用RT-PCR从人胎肝获得血小板生成素cDNA

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14、

METHODS � �-Lactamase genes including TEM, SHV, OXA-10 , PER, VEB, GES, CARB, IMP, VIM, SPM, GIM, DHA, FOX, MOX and oprD 2 were detected by PCR amplification in 33 PAE isolates.

方法对33株铜绿假单胞菌,采用PCR检测β - 内酰胺类药物耐药相关基因(TEM 、 SHV 、 OXA -10 群 、 PER 、 VEB 、 GES 、 CARB 、 IMP 、 VIM 、 SPM 、 GIM 、 DHA 、 FOX 、 MOX和OprD2).

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15、

Commonly methods of testing include GUS activity detection, PCR technology, hybridization, and immunological detection.

常用检测方法有GUS活性检测, PCR技术, 杂交检测, 免疫学检测.

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16、

Commonly methods of testing include GUS activity detection, PCR technology, hybridization, and immunological detection.

常用检测方法有GUS活性检测, PCR技术, 杂交检测, 免疫学检测.

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17、

RT-PCR was employed to measure the HIF-1α and VEGF mRNA expressions in gastrocnemii.

采用RT -PCR 法检测,半定量分析大鼠腓肠肌HIF -1 αmRNA和VEGFmRNA表达.

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18、

RT-PCR was employed to measure the HIF-1α and VEGF mRNA expressions in gastrocnemii.

采用RT -PCR 法检测,半定量分析大鼠腓肠肌HIF -1 αmRNA和VEGFmRNA表达.

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19、

Methods: Under a condition of heat stress, amplify HSP 70 gene from colon cancer cells by PCR.

方法在热应激条件下, 用PCR法从结肠腺癌细胞获取HSP70基因.

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20、

Methods: Under a condition of heat stress, amplify HSP 70 gene from colon cancer cells by PCR.

方法在热应激条件下, 用PCR法从结肠腺癌细胞获取HSP70基因.

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