1) potato leaves
马铃薯叶
1.
RP-HPLC method for determining the content of solanesol in the extracts of potato leaves
马铃薯叶中茄尼醇的RP-HPLC分析
2.
Solanesol was isolated and purified from the extracts of potato leaves by column chromatography,and RP-HPLC method was established for determining the content of solanesol.
通过柱色谱法从马铃薯叶的提取物中分离提纯了茄尼醇,并以RP-HPLC法测定了茄尼醇的质量分数。
2) potato leaf
马铃薯茎叶
1.
The volatile components of potato leaf (Solanum tuberosum L.
首次用顶空-固相微萃取-气相-质谱技术对马铃薯茎叶的挥发性成分进行了萃取和分析。
3) potato stems and leaves
马铃薯茎叶
1.
Comparison of two extraction methods of volatile compounds from potato stems and leaves
马铃薯茎叶挥发性成分的两种提取方法比较
2.
Adding biological agents have a great impact on the silage quality of potato stems and leaves.
采取因子完全区组实验设计,以7个不同含水量(鲜茎叶、80%、75%、70%、65%、60%、50%)的马铃薯茎叶为青贮原料,以不添加生物制剂处理与6种不同生物制剂(青贮体、乳酸菌、畜产1号、SL乳酸菌、牛用乳酸菌和酶贮制剂)为添加剂,进行马铃薯茎叶青贮饲料的感官评价和品质(pH值检测及评价、可溶性碳水化合物、干物质、粗蛋白质、纤维素、磷等)的系统监测,以及人工瘤胃下青贮饲料饲用价值(产气量和干物质消化率)的评价。
4) potato leafroll virus
马铃薯卷叶病毒
1.
Using RT-PCR-RFLP to detect and analysis potato leafroll virus;
马铃薯卷叶病毒RT-PCR-RFLP的检测分析
2.
The cDNA Cloning and Nucleotide Sequence Analysis of Potato Leafroll Virus Intergenic Region;
马铃薯卷叶病毒基因间隔区的克隆及序列分析
3.
One-step reverse-transcription polymerase chain reaction(RT-PCR) protocol for detection of potato virus X,potato virus Y and potato leafroll virus in infected potatoes and tobaccoes was developed.
运用一步法RT-PCR对马铃薯和烟草中的马铃薯X病毒、马铃薯Y病毒和马铃薯卷叶病毒进行了检测,实验表明:对酚-SDS方法提取的病毒核酸进行扩增,一步法RT-PCR检测到的扩增产物的灵敏度较两步法RT-PCR的高100倍左右。
5) PLRV
马铃薯卷叶病毒
1.
A pair of DNA primers were designed and synthesized based on the nucleotide sequence of potato leafroll virus(PLRV).
根据马铃薯卷叶病毒(PLRV)外壳蛋白基因的保守序列设计了一对寡聚核苷酸引物,从田间自然感染PLRV的马铃薯病株中提取病毒总RNA,用反转录-聚合酶链式反应扩增出符合设计大小240bp的特异性产物,而对照没有任何扩增产物。
6) potato leafroll virus (PLRV)
马铃薯卷叶病毒
1.
Total RNA of potato leafroll virus (PLRV) was extracted from virus-infected potato leaves collected from fields in Zhangjiakou of Hebei.
从典型的马铃薯卷叶病毒病株中直接提取出植物总RNA ,根据PLRV外壳蛋白基因序列 ,设计合成了一对寡核苷酸引物 ,经RT -PCR法扩增出全长的cDNA片段 ,将其克隆到质粒pGEM - 3Zf (+)上 ,并进行了序列分析。
2.
The intergenic sequence (IS) cDNA of Potato Leafroll Virus (PLRV) Chinese isolate was constructed into transformation binary vector pROK2 in positive or negative direction, then introduced into the commercial potato cultivar Desiree via Agrobacterium tumefaciens mediated gene transfer.
将本室合成、克隆的马铃薯卷叶病毒（ＰｏｔａｔｏＬｅａｆｒｏｌＶｉｒｕｓ，ＰＬＲＶ）中国分离株的基因间隔区（ｉｎｔｅｒｇｅｎｉｃｓｅｑｕｅｎｃｅ，ＩＳ）双链ｃＤＮＡ以正、反向两种方式分别构建于转化载体ｐＲＯＫ２中，通过致瘤农杆菌介导，以马铃薯叶圆片为转化材料，转化马铃薯栽培品种Ｄｅｓｉｒｅ，获得了转基因植株。
补充资料：马铃
1.系在马身上的铃铛。
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