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倪慧

作品数:5 被引量:12H指数:3
供职机构:中国农业大学农学与生物技术学院昆虫学系更多>>
发文基金:国家重点基础研究发展计划公益性行业(农业)科研专项更多>>
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A Comparative Study on Three Methods for the Extraction of Total RNA from Pinus bungeana被引量:3
2011年
[Objective] The aim of this study was to compare three RNA extraction methods and thus find out the suitable one for isolating intact and high quality total RNA from Pinus bungeana.[Method] Employing three extraction methods of Trizol,RNeasy Mini Kit,LiCl precipitation,total RNAs of P.bungeana were extracted from pine leaf samples,and their integrity and purity were detected via agarose gel electrophoresis and spectrophotometry for a comparative study.[Result] Among the three extraction methods,LiCl precipitation method demonstrated higher yield and better integrity of total extracted RNA,with OD260/OD280 ratio between 1.8-2.0 and clear 28 S and 18 S bands in electrophoresis pattern.[Conclusion] LiCl precipitation method could be used to extract highly pure and intact total RNA from P.bungeana.
王雁李贞刘小侠倪慧毛红张青文
棉铃虫β-微管蛋白基因cDNA序列的克隆与序列分析被引量:3
2012年
β-微管蛋白是构成细胞骨架的重要组成性蛋白,对昆虫的蜕皮、器官形成等生长发育阶段均能产生重要影响。本文以棉铃虫Helicoverpa armigera(Hübner)3日龄成虫为材料,利用RACE末端扩增技术克隆得到棉铃虫的β-微管蛋白基因的cDNA序列。序列分析表明:棉铃虫β-微管蛋白基因的cDNA序列包含1775个碱基,包括一个1347个碱基的开放阅读框,编码448个氨基酸组成的多肽。GenBank登录号:JF767013。同源性分析表明,棉铃虫的微管蛋白基因与本研究所比对其它昆虫的β-微管蛋白基因具有高度的同源性,达到90%左右。本研究克隆得到棉铃虫的β-微管蛋白基因的cDNA序列,对进一步深入研究该基因功能有重要意义。
闫硕刘小侠韩娜娜倪慧孙洁茹张青文
关键词:棉铃虫CDNA克隆微管蛋白
交配和黑光灯处理对棉铃虫Helicoverpa armigera生物钟基因cryptochromes mRNA表达的影响被引量:1
2011年
[目的]明确交配和黑光灯处理对棉铃虫生物钟基因cryptochromes mRNA表达的影响。[方法]应用实时定量PCR(SYBR Green)技术检测不同条件下棉铃虫cryptochromes(cry1和cry2)基因的表达。提取棉铃虫头部总RNA,经DNase I消化后进行反转录合成cDNA,并采用特异性引物分别对cry1、cry2和EF-1α基因进行实时定量PCR扩增。[结果]黑光灯处理棉铃虫2h,其cry1mRNA的表达量明显降低;cry2mRNA的表达量小于对照,但两者之间差异性并不显著。交配对棉铃虫cry1和cry2mRNA表达均存在显著影响,并且雌、雄两性cry1和cry2mRNA表达量在交配后随时间延长呈下降趋势。[结论]该结果对进一步研究cry基因的功能以及棉铃虫防治具有重要意义。
倪慧闫硕刘小侠张青文
关键词:棉铃虫交配
Cryptochromes mRNA Expression Under Mating and Black light Treatment on Helicoverpa armigera
2011年
[ Objective ] The paper was to confirm the effect of mating and black light treatment on cryptochromes mRNA expression of Hclicoverpa armigera. [ Method ] Quantitative real-time PCR ( SYBR Green) technique was applied to detect the expression of cryptochromes gene ( cryl and cry2 ) of H. armigera under different conditions. Total RNA was extracted from the head of H. armigera, and carried out reverse transcription to synthesize cDNA after digested by DNase I. Specific primers were used to carry out quantitative real-time PCR on cryl, cry2 and EF-Ict gene, respectively. [ Result] The expression of cryl mRNA of H. ar- migera significantly decreased after exposure to black light for 2 h, the mRNA expression of cry2 was smaller than control, they had no significant difference with each other. Mating had significant effect on mRNA expression of cryl and cry2 of H. armigera, and the mRNA expression of cryl and cry2 of male and female adults showed decreasing trend with the prolongation of time after mating. [ Conclusion] The result had important significance for further studying on function of cry gene and the control of cotton bollwonn.
倪慧闫硕刘小侠张青文
关键词:MATING
白皮松总RNA3种提取方法的比较研究被引量:5
2011年
[目的]对白皮松(Pinus bungeana)松针总RNA提取方法做比较,以得到完整的、高质量的白皮松总RNA。[方法]采用Trizol法、RNA提取试剂盒法和LiC l沉淀法3种方法提取白皮松总RNA,通过琼脂糖凝胶电泳和紫外分光光度计检测总RNA的完整性和提取纯度。[结果]LiC l沉淀法提取的RNA收率高,完整性好,OD260/OD280均在1.80~2.00,28S、18S条带清晰。[结论]LiC l沉淀法能高效地从白皮松针叶组织中分离出纯度高、完整性好的RNA样品。
王雁李贞刘小侠倪慧毛红张青文
关键词:白皮松总RNACDNA文库
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