1·Genes of ethylene receptor were cloned and characterized firstly in Arabidopsis Thaliana.
乙烯受体基因首先在拟南芥中被克隆并证实了其功能。
2·The invention discloses an aseptic water culture method applicable to Arabidopsis thaliana root system proteomics research.
本发明公开了一种适用于拟南芥根系蛋白质组学研究的无菌水培方法。
3·According to the results in Arabidopsis thaliana, both BOTERO and COBRA are required for normal orientation of cell expansion.
模式植物拟南芥中对BOTERO和COBRA的研究结果表明它们都是与细胞伸长方向有关的基因。
4·This review deals with the variation of testa luster as well as the mechanism of flavonoid biosynthesis in Arabidopsis thaliana .
在此，就拟南芥种皮的色泽变异及类黄酮生物合成机理作一介绍。
5·To test whether AtADCL in Arabidopsis thaliana has enzymatic activity, soluble form of the recombinant protein has to be obtained.
结果表明重组蛋白只在沉淀中表达即以包涵体形式存在。
6·The third part analyzes the genome structure of Arabidopsis thaliana and develops an ab initio eukaryotic gene recognition program.
论文的第三部分是真核生物基因识别和基因组结构分析。
7·Prediction of Arabidopsis thaliana secretome by the aid the combined computer - based software will accelerate the experimentally functional study of secretome.
通过相关生物信息学软件对拟南芥分泌蛋白组预测及功能的分类，将加速实验室对南芥分泌蛋白组功能的研究。
8·The function of gene has been identified using Prokaryotic expression system and Arabidopsis thaliana (A. thaliana) transformation systems. The study has got following results:1.
利用序列分析技术克隆与抗逆相关的基因，并通过原核表达体系和转基因技术进行功能验证。
9·The NPR1 gene was amplified from Arabidopsis thaliana genome DNA by DNA-PCR method. The DNA sequenced analysis showed that the sequence of amplified NPR1 gene was the same as the published sequence.
该文以DNA PCR扩增的方法，从拟南芥基因组DNA中克隆出NPR1基因，通过序列分析，所克隆的NPR1 基因与报道的基因序列完全一致。
10·CBF1 gene from rape was transformed into Arabidopsis thaliana by Agrobacterium tumefaciens-mediated method to screen its transgenic plants with resistance and conduct PCR detection and GUS staining.
采用根癌农杆菌介导法将油菜CBF1基因转入拟南芥，筛选抗性转基因拟南芥植株，进行PCR检测和GUS染色。