全文获取类型
收费全文 | 296篇 |
免费 | 7篇 |
国内免费 | 4篇 |
专业分类
林业 | 28篇 |
农学 | 36篇 |
基础科学 | 1篇 |
8篇 | |
综合类 | 166篇 |
农作物 | 28篇 |
水产渔业 | 1篇 |
畜牧兽医 | 10篇 |
园艺 | 22篇 |
植物保护 | 7篇 |
出版年
2022年 | 1篇 |
2021年 | 1篇 |
2020年 | 3篇 |
2019年 | 1篇 |
2017年 | 5篇 |
2016年 | 8篇 |
2015年 | 7篇 |
2014年 | 12篇 |
2013年 | 11篇 |
2012年 | 26篇 |
2011年 | 43篇 |
2010年 | 26篇 |
2009年 | 44篇 |
2008年 | 31篇 |
2007年 | 35篇 |
2006年 | 19篇 |
2005年 | 10篇 |
2004年 | 8篇 |
2003年 | 4篇 |
2002年 | 3篇 |
2001年 | 3篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1998年 | 2篇 |
1996年 | 1篇 |
1983年 | 1篇 |
排序方式: 共有307条查询结果,搜索用时 15 毫秒
31.
[目的]获取白术中高质量基因组DNA。[方法]选取新鲜白术叶片,破碎细胞壁,用经改良的CTAB与SDS法进行DNA分离纯化提取。[结果]改良CTAB法提取的DNA OD值为1.8~1.9,较改良SDS法的OD值(1.5~1.6)高。[结论]改良CTAB法提取的DNA浓度和纯度较高,可作为模板用于后续分子标记的研究。 相似文献
32.
核桃不同组织高质量总RNA的提取方法 总被引:3,自引:0,他引:3
利用改良CTAB法,分别从富含多糖、多酚及黄酮类物质的核桃叶、绿果、茎、种子和根中成功提取高质量的总RNA。经电泳、紫外分光光度计、RT-PCR和Northern杂交分析,结果显示,各组织的总RNA至少有2条清晰的电泳条带,产量可达174μg/g,A260/A280比值在2.0左右,通过RT-PCR在不同组织中均能扩增出核桃18S基因的cDNA片段,而且以18S基因为探针在不同组织中也分别获得清晰的Northern杂交信号,说明利用此法分离核桃各组织的RNA纯度和浓度完全符合后续分子生物学研究的要求。 相似文献
33.
Using pathogen-induced promoters to control expression of the functional genes in transgenic plants may greatly increase the chances of boosting disease resistance. However, the number of the inducible promoters is limited. Here, we found that soybean GmaSKTI36 gene is strongly induced upon Phytophthora sojae infection. Functional analysis showed that its promoter could mediate rapid and strong induction of GUS expression upon pathogen infection in both Nicotiana benthamiana leaves and soybean hairy roots. Then, a 122 bp fragment that was critical to the activity was successfully identified by a progressive 5′ deletion analysis. Importantly, we found that a synthetic promoter by tetramerizing this fragment could confer strong P. sojae induction activities. Overall, the results suggested that the GmaSKTI36 promoter, the 122 bp fragment, and the synthetic promoter are potentially useful pathogen-inducible promoters. 相似文献
34.
甘薯薯块富含淀粉、酚类等物质,不利于DNA提取。为了研究甘薯薯块DNA提取的最佳方法,采用经典CTAB法、改良CTAB法一、改良CTAB法二和SDS提取法,对甘薯薯块总DNA提取效果进行比较,以试剂盒法提取结果作对照。结果表明:采用经典CTAB提取法和SDS提取法获得的薯块DNA含有较多杂质,且降解严重,样品质量低;CTAB改良法一能降低DNA样品中多糖等物质的含量,但DNA存在一定程度降解,且耗时较长;CTAB改良法二提取效果最佳,杂质含量低且DNA降解少,与试剂盒提取效果最接近,是一种较为理想的甘薯薯块DNA提取方法。 相似文献
35.
Hans-Peter Rusterholz Sylvain Ursenbacher Armin Coray Urs Weibel Bruno Baur 《Journal of insect science (Online)》2015,15(1)
The sampling of living insects should be avoided in highly endangered species when the sampling would further increase the risk of population extinction. Nonlethal sampling (wing clips or leg removals) can be an alternative to obtain DNA of individuals for population genetic studies. However, nonlethal sampling may not be possible for all insect species. We examined whether remnants of traffic-killed specimens of the endangered and protected flighless longhorn beetle Iberodorcadion fuliginator (L., 1758) can be used as a resource for population genetic analyses. Using insect fragments of traffic-killed specimens collected over 15 yr, we determined the most efficient DNA extraction method in relation to the state of the specimens (crushed, fragment, or intact), preservation (dried, airtight, or in ethanol), storage duration, and weight of the sample by assessing the quantity and quality of genomic DNA. A modified cetyltrimethyl ammonium bromide method provided the highest recovery rate of genomic DNA and the largest yield and highest quality of DNA. We further used traffic-killed specimens to evaluate two DNA amplification techniques (quantitative polymerase chain reaction [qPCR] and microsatellites). Both qPCR and microsatellites revealed successful DNA amplification in all degraded specimens or beetle fragments examined. However, relative qPCR concentration and peak height of microsatellites were affected by the state of specimen and storage duration but not by specimen weight. Our investigation demonstrates that degraded remnants of traffic-killed beetle specimens can serve as a source of high-quality genomic DNA, which allows to address conservation genetic issues. 相似文献
36.
37.
一种改良的CTAB法提取马尾松基因组DNA 总被引:1,自引:0,他引:1
以马尾松针叶为试验材料,利用改良的CTAB法抽提基因组DNA,其浓度和纯度符合PCR实验的要求,经凝胶电泳检测,DNA纯化效果好。 相似文献
38.
39.
40.
一种改良的棉花总DNA提取方法 总被引:6,自引:0,他引:6
为了获取高质量的棉花基因组DNA,进行了后续分子实验,通过对已有的几种DNA提取方法进行综合比较,寻找一套优化的适于棉花高质量DNA的提取方法。结果表明,优化的棉花基因组DNA提取方法所提取的DNA纯度高,无降解现象,适用于进行常规PCR扩增以及进行高精度要求的SSR扩增。 相似文献