1) Bombyx mori single nuclear polyhydrosis virus
家蚕单(核壳体)核型多角体病毒
2) BmNPV
家蚕核型多角体病毒
1.
Study on Bombyx mori Nuclear Polyhedrosis Virus (BmNPV) Ubiquitin and Its Binding Peptides;
家蚕核型多角体病毒遍在蛋白及结合肽的研究
2.
Study on Bombyx Mori Nuclear Polyhedrosis Virus (BmNPV) Ubiquitin and Purification of Bombyx Mori Ubiquitin;
家蚕核型多角体病毒遍在蛋白及家蚕遍在蛋白的分离纯化
3.
Resistance to BmNPV of Transformation Cells Expressing Short lef-1 dsRNA
表达短lef-1 dsRNA的转化细胞对家蚕核型多角体病毒的抗性
3) Bombyx mori Nucleopolyhedrovirus (BmNPV)
家蚕核型多角体病毒
1.
【Objective】Studies were performed to investigate the inhibitory effects of different corresponding dsRNAs of gene gp64 on the multiplication of Bombyx mori Nucleopolyhedrovirus (BmNPV).
【目的】研究gp64基因相对应的多个dsRNA对家蚕核型多角体病毒增殖的抑制效果。
4) Bombyx mori nuclear polyhedrosis virus
家蚕核型多角体病毒
1.
Combination pathogenicity of Bacillus thuringiensis and Bombyx mori nuclear polyhedrosis virus to silkworms was investigated preliminarily, the results showed that BmNPV could enhance virulence of B.
t)和家蚕核型多角体病毒(Bombyxmorinuclearpolyhedrosisvirus,BmNPV)对家蚕的联合致病作用。
2.
A pair of primers was designed according to the conversed flanking sequence of p10 gene from BmNPV strain T3 and an 877 bp fragment was amplified by polymerase chain reaction (PCR) using genomic DNA extracted from Bombyx mori nuclear polyhedrosis virus Egyptian strain (BmNPVEg) as template.
根据BmNPVT3株中p10基因侧翼保守序列设计一对特异性引物,以家蚕核型多角体病毒埃及株(Bombyxmori nuclearpolyhedrosisvirusstrainEgyptian,BmNPVEg)基因组DNA为模板,应用PCR技术扩增得到p10基因(GenBank登录号:AF533970)。
3.
Bombyx mori nuclear polyhedrosis virus (BmNPV) as the main illness ofthe Bombyx mori has been studied for many fields .
本文利用家蚕核型多角体病毒(Bombyx mori Nuclear polyhedrosis virus,简称 BmNPV)感染多种农林业害虫,以期筛选出宿主域扩大的病毒株系。
5) Bombyx mori nuclear polyhedrosis virus (BmNPV)
家蚕核型多角体病毒
1.
To exploit the inhibition effect of RNAi on the replication and multiplication of Bombyx mori Nuclear Polyhedrosis Virus (BmNPV), we selected the immediate early gene 1 (ie-I), helicase and gp64 as the target genes, which play important roles in the replication and the horizontal transmission of BmNPV DNA.
为了探讨利用RNAi抑制病毒复制、增殖的效果,选取家蚕核型多角体病毒(BmNPV)对复制具有关键作用的极早期表达基因ie-1、解旋酶基因helicase以及对细胞释放型病毒(CRV)水平传播具有关键作用的病毒囊膜蛋白基因gp64为靶基因,体外合成了与其相对应的dsRNA,经脂质体转染家蚕BmN细胞,感染病毒粒子或共转染病毒基因组DNA,研究比较了供试dsRNA对BmNPV复制、增殖的抑制效果,探讨dsRNA分子大小以及同时抑制2个基因表达对病毒滴度的影响,筛选最佳标靶基因序列,为结合利用转基因技术和RNAi技术进行家蚕抗病毒研究提供依据。
6) Bombyx mori nucleopolyhedrovirus
家蚕核型多角体病毒
1.
We obtained the occlusion-derived virus(ODV) virion of Bombyx mori nucleopolyhedrovirus(BmNPV) by sucrose density gradient centrifugation,and used techniques of SDS-PAGE,2-DE and MS to identify the proteins present within or associated with ODV virion for the first time.
家蚕核型多角体病毒是引起家蚕病毒严重感染的关键病原之一,病毒与宿主的相互博弈一直是研究者们关注的问题。
2.
In order to know whether the red fluorescent protein(RFP) could be used as a molecular marker in baculovirus expression system,the open reading frame of rfp gene was cloned and inserted into Bombyx mori nucleopolyhedrovirus(BmNPV) genome.
尝试将红色荧光蛋白(RFP)作为昆虫表达体系的分子标签,克隆了rfp基因的读码框,通过Bac-to-Bac杆状病毒表达系统,将该基因插入家蚕核型多角体病毒(BmNPV)中,获得重组杆状病毒BmNPV-rfp。
3.
In order to explore whether transgenic technology and RNA interference can be used to enhance silkworm\'s resistance to Bombyx mori nucleopolyhedrovirus(BmNPV),the partial sequences of four BmNPV genes,namely DNA polymerase,protein kinase(PK1),bro-d and orf1629,were selected and used to prepare their inverted repeat sequences.
基于探讨利用转基因RNA干涉技术使家蚕获得对核型多角体病毒抗性的目的,将家蚕核型多角体病毒(BmNPV)的DNA聚合酶基因、蛋白激酶(PK1)基因以及bro-d和orf1629基因的部分编码片段,分别以其反向重复的形式与家蚕Actin3启动子连接,构建了基于piggyBac转座子载体的转基因表达载体,通过显微注射于家蚕卵,获得了36~107个G1蛾区,得到了20~23头转基因阳性家蚕。
补充资料：家蚕
| 家蚕 Bombyx mori 见桑蚕。 |
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条