多靶点RNAi载体,multiplesite targeting RNAi vector
1)multiplesite targeting RNAi vector多靶点RNAi载体
2)multiple RNAi element多靶点RNAi元件
3)FAD2-RNAi vectorFAD2-RNAi载体
4)RNAi vectorRNAi载体
1.The produced fragments were respectively introduced to the binary expressed vector pBI121 to produce pBI-PhrIP1 and to the GFP expressed vector pMON18342 to produce pMON-GFP-PhrIP1 and to theRNAi vector Hellsgate2 to produce Hellsgate2-PhrIP1,and then these plasmids were respectively mo.216kb的片段,分别克隆至双元表达载体、GFP载体和RNAi载体上,得到了植物超表达载体pBI-PhrIP1、GFP载体pMON-GFP-PhrIP1和RNAi载体Hellsgate2-PhrIP1。
2.The produced fragments were respectively introduced to the binary expressed vector pBI121 to produce pBI-Ran2 andRNAi vector Hellsgate2 to produce Hellsgate2-Ran2.根据编码拟南芥小GTP结合蛋白的Ran2基因cDNA全序列设计超表达引物和序列内部第397~610bp之间序列设计RNAi引物,以pMD18-T-Ran2为模板,用PCR方法分别扩增出666bp和214bp的片段,分别连接至双元表达载体和RNAi载体上,得到了植物超表达载体pBI-Ran2和RNAi载体Hellsgate2-Ran2,并用电转化法导入农杆菌GV3101菌株中,PCR扩增结果表明所构建的植物超表达载体pBI-Ran2和RNAi载体Hellsgate2-Ran2已导入农杆菌。
3.In order to efficiently identify the functions of ZmPti1 gene,two plant-transformation vectors,pBPC-ZmPti1-bar(sense expression vector)and pBPC-PtS-GFP-PtAs-bar(RNAi vector)were prepared.构建了ZmPti1基因的正义表达载体和RNAi载体,以bar基因为抗性筛选标记,通过花粉管通道法将构建的两个表达载体分别转化到玉米自交系178。
英文短句/例句
1.Cloning of BBE gene of Papave somniferum and construction of its RNAi expression vector野生罂粟BBE基因克隆及RNAi载体构建
2.Cloning of Pollen Fertility Gene MS2 and Construction of Its RNAi Expression Vector花粉育性基因MS2的克隆与RNAi载体构建
3.Construction of the RNAi Vector Carrying BnCr4 Gene and Transformation of Brassica napus L.油菜BnCr4基因RNAi载体构建及植株转化
4.Isolation, Expression and Construction RNAi Vector of Drought-Resistant Related Genes in Mongolian Wheatgrass蒙古冰草抗旱相关基因克隆、表达及RNAi载体构建
5.Cloning and RNAi Vector Construction of Gene Fragments Related to Lignin Metabolism of Miscanthus芒木质素代谢基因片段的克隆及RNAi载体构建
6.Construction of Mongolian Wheatgrass LEA3 Gene in RNAi Expression Vector蒙古冰草LEA3基因RNAi表达载体的构建
7.Advance in RNAi Mediated with Lentivirus-based Vectors慢病毒载体介导RNAi的研究进展
8.Construction of RNAi plant expression vectors in transgenic watermelon resistant to viruses西瓜抗病毒RNAi植物表达载体的构建
9.Construction and identification of lentiviral vector of RNA interference of CDC25B3 geneCDC25B_3基因RNAi慢病毒载体的构建与鉴定
10.Construction and Functional Identification of pSUPER Vector of p21 RNAip21 RNAi的pSUPER载体的构建及功能鉴定
11.Construction and identification of lentiviral vector-mediated RNA interference of SATB1 geneSATB1基因RNAi慢病毒载体的构建与鉴定
12.Construction and identification of lentiviral vector encoding shRNA against Smad3Smad3基因RNAi慢病毒载体的构建与鉴定
13.Construction and identification of lentiviral vector of RNA interference of GFβ1 geneTGFβ1基因RNAi慢病毒载体的构建与鉴定
14.Construction of lentivector-mediated RNAi and it efficiently downregulates expression of murine TNF-α gene in vitro小鼠TNF-α基因RNAi慢病毒载体的构建及体外研究
15.Construction and identification of lentivial RNA interference vector of rat leptin receptor gene大鼠瘦素受体RNAi慢病毒载体的构建及鉴定
16.The Construction of Expressing Vector shRNA/mdr1 and a Study on Multidrug Resistance Reversal of Human Hepatocellular Carcinoma by RNA Interference;shRNA/mdr1表达载体构建及RNAi逆转肝细胞癌多药耐药
17.The Inhibitory Effects of Survivin Expression Vector of HL-60 Cells by RNAi;Survivin基因RNAi真核表达载体对HL-60细胞的抑制作用
18.Inhibition Effect of RNAi on CTCF Expression by Adeno-associated Virus Vector;腺相关病毒载体介导的RNAi抑制CTCF的表达
相关短句/例句
multiple RNAi element多靶点RNAi元件
3)FAD2-RNAi vectorFAD2-RNAi载体
4)RNAi vectorRNAi载体
1.The produced fragments were respectively introduced to the binary expressed vector pBI121 to produce pBI-PhrIP1 and to the GFP expressed vector pMON18342 to produce pMON-GFP-PhrIP1 and to theRNAi vector Hellsgate2 to produce Hellsgate2-PhrIP1,and then these plasmids were respectively mo.216kb的片段,分别克隆至双元表达载体、GFP载体和RNAi载体上,得到了植物超表达载体pBI-PhrIP1、GFP载体pMON-GFP-PhrIP1和RNAi载体Hellsgate2-PhrIP1。
2.The produced fragments were respectively introduced to the binary expressed vector pBI121 to produce pBI-Ran2 andRNAi vector Hellsgate2 to produce Hellsgate2-Ran2.根据编码拟南芥小GTP结合蛋白的Ran2基因cDNA全序列设计超表达引物和序列内部第397~610bp之间序列设计RNAi引物,以pMD18-T-Ran2为模板,用PCR方法分别扩增出666bp和214bp的片段,分别连接至双元表达载体和RNAi载体上,得到了植物超表达载体pBI-Ran2和RNAi载体Hellsgate2-Ran2,并用电转化法导入农杆菌GV3101菌株中,PCR扩增结果表明所构建的植物超表达载体pBI-Ran2和RNAi载体Hellsgate2-Ran2已导入农杆菌。
3.In order to efficiently identify the functions of ZmPti1 gene,two plant-transformation vectors,pBPC-ZmPti1-bar(sense expression vector)and pBPC-PtS-GFP-PtAs-bar(RNAi vector)were prepared.构建了ZmPti1基因的正义表达载体和RNAi载体,以bar基因为抗性筛选标记,通过花粉管通道法将构建的两个表达载体分别转化到玉米自交系178。
5)RNAi plasmid vectorRNAi质粒载体
6)RNAi expression vectorRNAi表达载体
延伸阅读
FAD-Na2分子式：C27H31N9Na2O15P2分子量：829.52CAS号：84366-81-4性质：水溶性5 g/L。
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