快速扩增技术,GeneRacer英语短句,例句大全

快速扩增技术,GeneRacer
1)GeneRacer快速扩增技术
1.Its full-length was amplified by GeneRacer rapid amplification of cDNA ends.方法根据本实验室已经克隆的家蝇抗菌肽基因diptericin片段设计1对引物,运用cDNA末端快速扩增技术(GeneRacer)、T-A克隆和序列测定,将所得序列与GenBank中已知的diptericin基因进行同源性分析。
2)RACE[英][re?s][美][res]cDNA末端快速扩增技术
1.To understand the mechanism of chick focal adhesion kinase gene(FAK)expression and regulation,the transcription start sites and four kinds alternatively spliced 5′end(5′untranslated region,5′UTR)of FAK mRNA in chick embryo fibroblast cells were identified by RACE.为了研究鸡局部黏着斑激酶(FAK)基因表达调控的分子机制,运用cDNA末端快速扩增技术确定了鸡胚成纤维细胞FAK基因的转录起始位点,并发现FAK基因mRNA的5′非翻译区(5′UTR)存在4种剪切形式。
2.Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning of full-length cDNA 5 and 3 ends after a partial cDNA sequence has been obrained by other methods.cDNA末端快速扩增技术是一种基于多聚酶链式反应的技术 ,它的发展大大便利了应用其它方法获得的部分cDNA序列后克隆全长cDNA 5’和 3’末端的工作。
3.This study has cloned Grass carp The full-length cDNA of CRP by the methods of RACE and analysed the sequences, And the CRP tissue distribution was detected in the Grass carp different tissue With the method of RT-PCR,as well as Prokaryotic Expression vector of CRP was suceessfully to be constructed.本研究采用cDNA末端快速扩增技术(RACE)’对草鱼C反应蛋白基因的cDNA全长序列进行克隆,序列分析,并通过RT-PCR方法研究了草鱼CRP组织分布,同时成功构建了草鱼CRP原核表达重组质粒。
3)rapid breeding technique快速扩繁技术

英文短句/例句

1.Study on Breeding Technology by Seedlings to Seedlings of Carya illinoensis美国山核桃以苗繁苗快速扩繁技术研究
2.Study on Atractylodes macroephala Koidz By Tissue Culture and Rapid Propagation;祁术的组织培养及快速繁殖技术研究
3.Study on in vitro rapid propagation technology of chinese short cherry中华矮樱桃试管苗快速繁殖技术研究
4.STUDY ON RAPID PROPAGATION OF ZANHUANG CHINESE DATE BY TISSUE CULTURE赞皇大枣组织培养快速繁殖技术研究
5.Study on the Technology of Rieger Begonia Micropropagation丽佳秋海棠组培快速繁殖技术的研究
6.On the Fast Reproduction Technology of Tissue & Culture for Chrysanthemum- green Beauty;菊花-绿美人组织培养的快速繁殖技术
7.Fast Breed Tech of Medicinal Herbs;药用植物重楼快速繁殖技术研究前景
8.Studies on Rapid Propagation Technology of 2 Step ways of 4 Floribunda Roses Cultivars;丰花月季的两步法快速繁殖技术研究
9.The Technology Study on Tissue Culture and Rapid Propagation of Oncidium;文心兰(Oncidium)微体快速繁殖技术的研究
10.The Cultivation and Vitro Rapid Propagation of the Test Tube Seedlings of Musa AAA Red Green;红皮香蕉试管苗快速繁殖及栽培技术
11.Study on the Tissue Culture and Rapid Multiplication of Kerria japonica棣棠花组织培养与快速繁殖技术研究
12.Study on tissue culture and micropropagation of Dendrobium pierardii瀑布兰组织培养快速繁殖技术的研究
13.Fast Acquisition Technology to the Spread Spectrum Signal Based on the FFT基于FFT的扩频信号快速捕获技术研究
14.A Research on the Tissue Culture and Rapid Propagation of Opuntia Milpa Alta Haw食用仙人掌组织培养及快速繁殖技术研究
15.Study on Technique System of Tissue Culture and Rapid Propagation of Cherry樱桃组织培养和快速繁殖技术体系的研究
16.Tissue Culture and Rapid Propagation of Acer Ginnala;茶条槭（Acer ginnala）组织培养与快速繁殖技术研究
17.Study on the Technique in Vitro of Mornordica Charantia (Lvren);‘绿人’苦瓜离体快速繁殖技术体系的研究
18.Rapid Propagation Protocol in the Culture of Cymbidium Kanran Makino and in Vitro Flowering;寒兰快速繁殖技术及其试管成花的研究

相关短句/例句

RACE[英][re?s][美][res]cDNA末端快速扩增技术
1.To understand the mechanism of chick focal adhesion kinase gene(FAK)expression and regulation,the transcription start sites and four kinds alternatively spliced 5′end(5′untranslated region,5′UTR)of FAK mRNA in chick embryo fibroblast cells were identified by RACE.为了研究鸡局部黏着斑激酶(FAK)基因表达调控的分子机制,运用cDNA末端快速扩增技术确定了鸡胚成纤维细胞FAK基因的转录起始位点,并发现FAK基因mRNA的5′非翻译区(5′UTR)存在4种剪切形式。
2.Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning of full-length cDNA 5 and 3 ends after a partial cDNA sequence has been obrained by other methods.cDNA末端快速扩增技术是一种基于多聚酶链式反应的技术 ,它的发展大大便利了应用其它方法获得的部分cDNA序列后克隆全长cDNA 5’和 3’末端的工作。
3.This study has cloned Grass carp The full-length cDNA of CRP by the methods of RACE and analysed the sequences, And the CRP tissue distribution was detected in the Grass carp different tissue With the method of RT-PCR,as well as Prokaryotic Expression vector of CRP was suceessfully to be constructed.本研究采用cDNA末端快速扩增技术(RACE)’对草鱼C反应蛋白基因的cDNA全长序列进行克隆,序列分析,并通过RT-PCR方法研究了草鱼CRP组织分布,同时成功构建了草鱼CRP原核表达重组质粒。
3)rapid breeding technique快速扩繁技术
4)rapid technology快速技术
5)PCR amplification techniquePCR扩增技术
6)RACE[英][re?s][美][res]快速cDNA末端扩增
1.The rapid amplification of cDNA ends(RACE)technique and the electronic cDNA library select mathod was applied to amplify full length of the expressing sequence tag(EST) ,which is a specfic-stage in Schistosoma japonicum adult worm, and a cDNA fragment with an ORF was identified(GenBank accession number is AY847290).利用快速cDNA末端扩增(RACE)技术结合“电子cDNA文库”筛选法,对日本血吸虫成虫期特异表达基因EST片段的全长序列进行了扩增,获得了一含完整开放性阅读框(ORF)的基因序列(GenBank中的登录号为AY847290)。