3'RACE法,3'RACE
5-RACE and 3-RACE5'-RACE与3'-RACE方法
3)3 RACE3'RACE
1.3 RACE Amplification and Sequence Analysis of a Strain of Norovirus;一株诺如病毒的3’RACE扩增及基因序列分析
2.Objective:To amplify the 3 -cDNA end of phospholipase D(PLD)gene of Agropyron mongolicum Keng by 3 RACE technique and to analyze the sequence in the experiment,the 3 -cDNA end cloning establish foundation in order to obtain the cDNA sequence and research the function of PLD gene.目的:采用3’RACE方法对蒙古冰草磷脂酶D(PLD)基因3’端全序列进行了快速扩增和序列分析,为得到全序列及研究该基因的功能奠定基础。
3.The cDNA of DMrt1(DM-related transcription factor1)was amplified by 3 RACE-PCR(Rapid Amplification of cDNA Ends-Polymerase chain reaction)strategy using the total isolated RNA as template.从奥利亚罗非鱼精巢提取总RNA,采用RT和3’RACE(rapid amplification of cDNA ends)法分离和测定了奥利亚罗非鱼DMRT1(DM-related transcription factor1)cDNA的3’序列,扩增得到1086bp的片段,阅读框共编码254个氨基酸,序列分析结果表明,奥利亚罗非鱼DMRT1基因的氨基酸序列与尼罗罗非鱼DMRT1基因的同源性为99%,与黑鲷、黄鳝、新月鱼、虹鳟、青鳉鱼等动物的DMRT1cDNA和尼罗罗非鱼、奥利亚罗非鱼等动物的DMO(DM-domain gene in Ovary)cDNA的同源性分别为:80%、78%、73%、62%、41%、26%、26%。
4)3'-RACE3-'RACE
1.In this study,a cDNA fragment of dehydroascorbate reductase(DHAR) including whole 3 -end was cloned from Royal Gala by RT-(nest) PCR and 3′-RACE.以皇家嘎拉苹果叶片为材料提取总RNA,合成cDNA第一链后,先利用巢式PCR获得苹果脱氢抗坏血酸还原酶(DHAR)基因中间片段,再利用3-′RACE方法进一步获得3′末端核酸序列,共得到840 bp包含完整3′末端的DHAR基因cDNA片段,其序列与烟草、水稻、番茄中DHAR基因序列的同源性均大于70%,证明所克隆到的核苷酸片段确为苹果DHAR基因cDNA片段。
5)3-RACE3'-RACE
1.Amplification Carbo-tip of L Gene by 3 -RACE and Sequence Analysis of Rabies Virus;RV野毒株L基因C端3’-RACE扩增及序列分析
2.Methods:An objective gene was isolated by using a RT-PCR and 3 -RACE approachs and two degenerate PCR primers against conserved sequences in the MADS-box and in the C-terminal region of several plants.方法:根据多种植物的MADS-box保守区及其C-端序列设计一对简并性引物,利用RT-PCR及3’-RACE的方法分离目的基因。
6)3 RACE or 5 RACE3 RACE或5 RACE
延伸阅读

[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]分子式:C16H16ClN3O3S分子量:365.5CAS号:26807-65-8性质:暂无制备方法:暂无用途:用于轻、中度原发性高血压。