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apis
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  蜜蜂
     Expression of Prepromelittin Gene of Apis cerana cerana in Tn-5B1-4 cell
     中华蜜蜂前溶血肽原基因在Tn-5B1-4细胞中的表达
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     The breeding proportion of Apis cerena cerena to local apis population was 41.5%, 36.8%, 3.1% and 1.1%, and that of Apis mellifera Ligustica was 58.5%, 63.2%, 96.9% and 98.9% in the mountainous areas of south and west Anhui, Jianghuai area, and Huaibei plain, respectively.
     皖南山区、皖西大别山区、江淮地区和淮北平原,中华蜜蜂分别占本地区蜂群的41·5%、36·8%、3·1%和1·1%,意大利蜜蜂分别占本地区蜂群的58·5%、63·2%、96·9%和98·9%.
短句来源
     Cloning and Functional Prediction of ant Gene and vha16 Gene From Honeybee(Apis mellifera) Based on Bioinformatics
     蜜蜂(Apis mellifera)ant基因和vha16基因的克隆及其功能预测的生物信息学研究
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     Sequence and Expression of MRJPs cDNA from Apis Cerana Cerana
     中华蜜蜂(Apis cerana cerana)王浆蛋白cDNA的序列分析及表达
短句来源
     The results showed that the mean content of DNA extracted from fresh royal jelly of Apis cerana was(82.95 ±10.39)μg/g,the mean purity(A_260/A_280)was 1.69±0.08.Taking the DNA as the template for RAPD-PCR,the obtained bands were clear,bright and complete.
     结果表明:中华蜜蜂新鲜王浆中DNA的含量为66.29~105.34μg/g,平均含量为(82.95±10.39)μg/g,平均纯度(A260/A280)为1.69±0.08,以其作为模板进行RAPD-PCR扩增,扩增的条带较清晰、明亮、稳定性好。
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  蜜蜂属
     Molecular cloning of Apis cerana cerana MRJP2 and comparative analysis of C-terminal repetitive sequences of MRJP2 among six species in Apis genus
     中华蜜蜂MRJP2基因克隆及蜜蜂属(Apis)六蜂种间MRJP2基因C-端重复序列比较分析
     Comparative Study of Esterase Isozymes in Six of Apis
     蜜蜂属(Apis)六个种酯酶同功酶的研究
短句来源
     THE CLASSIFICATION,DISTRIBUTION,AND CHARACTERISTICS OF MORPHOLOGY AND BIOLOGY OF BEE SPECIES IN GENUS APIS
     蜜蜂属内蜂种的分类、地理分布、形态特征和生物学特性
短句来源
     The C-terminal repetitive sequences of MRJP2 were also cloned and sequenced in other five species in Apis genus. The results showed that the sequences of the C-terminal repetitive fragment performed individual polymorphism based on core bases mutation instead of different duplications in the other five species, while the lengths of the repetitive sequences are almost the same among different individuals belong to one species.
     克隆并测定了蜜蜂属(Apis)内其他五个种的MRJP2基因的C-端重复序列,结果表明,在蜜蜂属的其他五个种中,C-端重复片段的核心序列是以碱基高度突变方式而表现出个体之间的多态性,而重复片段长度基本一致。
     Esterase isozymes of the samples of Hymenoptera collected from Beijing and Yunnan were investigated with isoelectric forcusing electrophoresis with polyacrylamide gel. The samples covered 7 superfamilies of Hymenoptera, 9 genera of Apoidea, 6 species of Apis and 4 races of Apis mellfern.
     用聚丙烯酰胺凝胶等电聚焦电泳分析了膜翅目七个总科、蜜蜂总科9个属,蜜蜂属6个种和西方蜜蜂4个宗样品的酯酶同工酶。
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  “apis”译为未确定词的双语例句
     Wireless Web Services Application Security Based on Bouncy Castle Crypto APIs
     基于Bouncy Castle Crypto API的无线Web Services应用安全
短句来源
     The temperature signal was captured by sensor PT_1000 and 16 bit AD LTC1606.The program was designed by U'nsp IDE APIs and the water temperature was controlled by using SPCE061A.
     由传感器PT_1000和16位AD LTC1606获取温度信号,使用U'nsp IDE环境提供的API函数进行控制程序设计,通过SPCE061A实现温度实时控制.
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     The Study of the Mapping of Call Concepts Between Parlay APIs and SIP
     Parlay APIs与SIP间呼叫相关概念映射的研究
短句来源
     The longest variable times that Apis mellifera ligustica eggs could develop were 4h at 15, 18, 21℃, 8h at 24, 27℃, 20h at 30℃, 2h at 40℃.
     意蜂卵为:15、18、21oC为4h,24、27℃为sh,30,C为20h,40oC为Zh。
短句来源
     The paper focuses on the research of OSS/J APIs, and applies OSS/J Service Activation API to an eTOM-based Service Provisioning System, according to the principle of NGOSS and OSS/J.
     本论文对OSS/J尤其是Service Activation API进行了重点研究,并在对NGOSS、OSS/J的研究基础上,将SAAPI应用到一个基于eTOM标准的服务开通系统中。
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  apis
Polymorphism of Locus COI-COII of Mitochondrial DNA in the Honeybee Apis mellifera L.
      
In spite of high biodiversity within the honeybee species Apis melliferaL., only one geographical race, the dark-colored forest honeybee A.
      
Local honeybee (Apis mellifera mellifera L.) populations in the Urals
      
The COI-COII intergenic region of mitochondrial DNA (mtDNA) was studied in local honeybee (Apis mellifera mellifera) L.
      
For the Chinese honeybee (Apis cerana cerana F.) a phylogenetic dendrogram has been constructed in which 4 subfamilies are clustered based on DNA fingerprint patterns.
      
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It has been experienced that in Peking immediately after the soil is defrozen in the spring, no trace of soft-rot bacteria can be isolated from the field soil, although this organism can be readily isolated from the undecomposed residues of the Chinese cabbage in the field, if there is any. The soft rot of the Chinese cabbage in cellar develops throughout the storage period. It is therefore convinced that the-primary source of infection of the soft rot of the Chinese cabbage is either from the undecomposed residues...

It has been experienced that in Peking immediately after the soil is defrozen in the spring, no trace of soft-rot bacteria can be isolated from the field soil, although this organism can be readily isolated from the undecomposed residues of the Chinese cabbage in the field, if there is any. The soft rot of the Chinese cabbage in cellar develops throughout the storage period. It is therefore convinced that the-primary source of infection of the soft rot of the Chinese cabbage is either from the undecomposed residues from the field or from the debris in the cabbage cellar. The seed Chinese cabbage from the cellar after overwintering is planted out at the end of march and meanwhile carries the soft rot organisms to the field. Furthermore, a number of insects serves as spreaders. Isolations of a number of insects found either in cabbage cellar or in spring cabbage fields reveal that 76% of Sarcophaga sp., 66.8% of Fannia sp., 4% of Apis mellifera, 40% of Athalia rosae and 30% of Plutella maculipennis are found to carry soft-rot organisms both externally and internally. The results of an field experiment point out that the early diseased cabbage plants in the field serve as centers of infection of the soft-rot disease. The bacteria are disseminated in the field by the irrigation water. However, only those cabbage plants which are wounded at the basal part are liable to the attack. It is therefore suggested that in addition to the control of insect pests in connection with the adequate cultural practice, the thoroughness of eliminating the centers of infection by prompt removal of the diseased plants from the field every time before irrigation must be observed. In the present paper a rapid method for determining the pathogenic soft-rot bacteria from the soil is described.

白菜軟腐細菌Erivinia aroideae不能在田間土壤中越冬,但能在未分解的病菜根和病菜叶中越冬。用病根及病叶等所作的堆肥中不能分离出具有致病力的軟腐細菌。菜窖中的废菜叶为軟腐細菌越冬及繁殖的主要場所之一?杭居陕橛?Sarcophaga sp.)及花蝇(Fannia sp.)传布到田間的感病作物上,另外也可以由蜜蜂(Apis mellifera L.)、叶蜂(Athalia rosae L.)及小菜娥(Plutella maculipennis curtis)等繼續在白菜間传布。此外窖中移出的菜种株上亦带有病原細菌。因此認为菜窖中及田間殘菜根的越冬細菌是軟腐病的初次侵染源。菜畦內发生的早期病株是軟腐細菌的供給者。凡是畦內菜株受伤而有早期病株时全畦发病最重;畦內菜株无伤而无早期病株时发病最輕。在菜株受伤的情况下,早期病株的影响特别显著。灌溉水有在畦內传布病原細菌的能力。建議在防治中結合栽培及防虫必須注意在每次灌水前及早拔除早期病株,以增进防治的效果。

A qualitatve paper chromatographic analysis of the amino acids in royal jelly of the honey bee (Apis indica) has been investigated. The proteins of royal jelly from Apis indica were precipited with 95% ethyl alcohol. The proteins were hydrolyzed with 0.38N Ba(OH)_2 or 6NHCl. Aliquots of the hydrolyzates were chromatographed. Aspartic acid, glutamic acid, lysine, arginine, histidine, glycine, serine, threonine, alanine, tyrosine, methionine, valine, tryptophan, isoleucine, leucine, phenylalanine,...

A qualitatve paper chromatographic analysis of the amino acids in royal jelly of the honey bee (Apis indica) has been investigated. The proteins of royal jelly from Apis indica were precipited with 95% ethyl alcohol. The proteins were hydrolyzed with 0.38N Ba(OH)_2 or 6NHCl. Aliquots of the hydrolyzates were chromatographed. Aspartic acid, glutamic acid, lysine, arginine, histidine, glycine, serine, threonine, alanine, tyrosine, methionine, valine, tryptophan, isoleucine, leucine, phenylalanine, proline, and cystinc were identified in the protein hydrolyzates.

1.本文概述了王浆的化学成分,营养价值、医疗性能以及中蜂王浆的生产过程。 2.应用新华定性层析沪紙作紙上层析,初步鑑定了中蜂王浆蛋白貭的氨基酸組成有門冬氨酸,谷氨酸,賴氨酸,精氨酸,組氨酸,甘氨酸,絲氨酸,苏氨酸,丙氨酸,酪氨酸,甲硫氨酸,缬氨酸,色氨酸,异亮氨酸,亮氨酸,苯丙氨酸,脯氨酸,胱氨酸共18种。

The haemolymph protein patterns of two species of honeybees, Apis mellifera and Apis cerana were investigated with polyacrylamide gel disc electrophoresis and were shown to be quite similar. The haemolymph protein pattern of the worker bees of Apis mellifera shows eleven bands typically; there are certain differences in different castes, developmental stages and between the species. Band V of the female bees is vitellogenin which is either absent in the drones or present only in traces. This...

The haemolymph protein patterns of two species of honeybees, Apis mellifera and Apis cerana were investigated with polyacrylamide gel disc electrophoresis and were shown to be quite similar. The haemolymph protein pattern of the worker bees of Apis mellifera shows eleven bands typically; there are certain differences in different castes, developmental stages and between the species. Band V of the female bees is vitellogenin which is either absent in the drones or present only in traces. This band of vitellogenin is most prominent in the egg-laying queens. Band XI is a larval protein, most prominent in the larval stage, gradually disappears in the adult stages of Apis cerana, but is still present in the adult stages of Apis mellifera. The hamolyinph protein pattern of the pupa is characterised by having many indistinct bands, probably representing disintegrating proteins during histolysis. The molecular weight of the vitellogenin of Apis mel-lifera was determined to be 185,000 with Thorun's method.

本实验用聚丙烯酰胺凝胶电泳分析了两个蜂种的血淋巴蛋白质成分。意蜂和中蜂都是Apis属,血淋巴蛋白质电泳谱相似。但是,两蜂种以及同一蜂种不同级别、不同发育阶段的电泳谱又各有特点。根据实验,我们把成年蜂血淋巴电泳谱分为11条带,雌蜂电泳谱上的带5是卵黄原蛋白;雄蜂卵黄原蛋白含量很少或测不出。 用Thorun方法,在聚丙烯酰胺凝胶平板电泳上测得意蜂卵黄原蛋白的分子量为185,000。

 
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