1) Pear vein yellow virus(PVYV)
梨脉黄病毒
1.
The double-strand RNA(dsRNA)from fresh,refrigerated(4℃2～4days),freezen leaf and bark of Korlaxiangli pear variety infected with Pear vein yellow virus(PVYV)and virus-free seedling were extracted respectively.
用已知带梨脉病毒(Pearveinyellowvirus,PVYV)的库尔勒香梨植株和库尔勒香梨无病毒实生苗为供试材料,分别选用新鲜幼嫩叶片、4℃条件下保存2～4d的幼嫩叶片、冷冻的幼嫩叶片和皮层为试材,进行dsRNA的分离提取实验,得到了与PVYV基因组RNA长度9306bp相当大小的dsRNA谱带,并以dsRNA为模板,利用设计的特异引物,研究建立了梨脉黄病毒(PVYV)的RT-PCR检测技术体系,能有效地扩增出PVYV的一条长为316bp的特异片段,该技术可广泛用于果树病毒的分子检测。
2) pear vein yellow virus (PVYV)
梨脉黄病毒(PVYV)
3) Malvastrum yellow vein virus (MYVV)
赛葵黄脉病毒
1.
Partial DNA-A sequence of Y200 is closely related to that of Malvastrum yellow vein virus (MYVV) DNA-A with 96.
对其DNAA基因组部分序列测定分析表明,该序列与赛葵黄脉病毒Malvastrumyellowveinvirus(MYVV)相应序列的同源性为96。
4) Ageratum yellow vein virus
胜红蓟黄脉病毒
1.
The material used in this thesis, which is termed Ageratum yellow vein virus-Fujian isolate F1 (AYVV-[F1]), is the first report of geminivirus found in Fujian.
本文以福建省首例发现的胜红蓟黄脉病毒AYVV(登录号EF544600)为研究对象,通过双生病毒卫星小分子DNAβ的通用引物,PCR扩增获得AYVV-[F1]的完整DNAβ分子。
5) Beet Necrotic Yellow Vein Virus
甜菜坏死黄脉病毒
1.
RT-PCR Detection for Beet Necrotic Yellow Vein Virus (BNYVV);
应用RT-PCR技术检测甜菜坏死黄脉病毒
2.
The RNA was extracted from purified beet necrotic yellow vein virus (BNYVV) isolated from Inner Mongolia.
以来自于我国内蒙古、黑龙江和宁夏的3个甜菜坏死黄脉病毒(BNYVV)分离物为材料,采用反转录-PCR方法扩增不同RNA组分的基因片段,经cDNA克隆和序列测定后,与国外报道的BNYVV不同株系和来自于我国不同地区的BNYVV分离物之间进行比较分析。
3.
Spontaneously deleted RNA2, RNA3 and RNA4 cDNA clones were obtained respectively by cloning the RT PCR products of beet necrotic yellow vein virus NM isolate from Inner Mongolia into pGEM 7Zf(+).
以甜菜坏死黄脉病毒内蒙分离物 (BNYVVNM )总RNA为模板 ,经RT -PCR扩增 ,分别获得RNA2、RNA3和RNA4自然缺失突变体的cDNA克隆。
6) Lindernia anagallis yellow vein virus
长蒴母草黄脉病毒
补充资料：黄梨洲(见黄宗羲)
黄梨洲(见黄宗羲)
Huang Lizhou (Huang Li-chou)
HUongLjZ卜。u黄梨洲见黄宗羲。
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