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1.immunologically competent cell
免疫活性细胞收藏指正
2.One RING domain and two BIRs domain contained in IAP2 while one RING and one BIR domain contained in IAP3.iap2 and iap3 were ligated into expression vector pET-28a, then were transformed into BL21(DE3) competent cell respectively.
用表达载体pET28a-iap2转化宿主菌BL21(DE3)感受态细胞,挑取单菌落并接种于加卡那霉素的LB中,扩大培养后加入IPTG诱导表达,表达结果显示,含iap2基因载体的表达产物在电泳中出现一条约40kDa的表达带,与理论推测的蛋白分子量一致。收藏指正
3.Methods The replication-competent HBV recombinant plasmid pHBV4.1 plus different liver-enriched transcription factor (HNF1,HNF3,HNF4,HNF6,C/EBP and RXRα/PPARα) expression plasmids were co-transfected into nonhepatic cell lines (NIH3T3,HeLa,293T,SW1353,CV-1 and COS1).
方法用复制型HBV重组质粒PHBV4.1与肝富集转录因子HNF1、HNF3、HNF4、HNF6、C/EBP或RXRΑ/PPARΑ的表达质粒,分别共转染非肝源细胞株NIH3T3、HELA、293T、SW1353、CV-1和COS1。收藏指正
4.To construct the Baculovirus expression vector for translationally controlled tumor protein (TCTP) gene of Schistosoma japonicum and to express in insect sf9 cell line, the TCTP eDNA was cloned into plasmid pFASTA, and therecombinant plasmid was transformed to competent cells DH10Bat.A transformant containing the target gene was obtained and named as BacmidGFP-SjTCTP.
目的构建日本血吸虫的翻译控制肿瘤蛋白(SjTCTP)基因的杆状病毒重组供体质粒pFASTA-TCTP,用该重组转移质粒转化含有杆状病毒表达载体以构建BacmidGFP-TCTP,感染昆虫细胞进行表达。收藏指正
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