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amplification相关的网络例句

查询词典 amplification

与 amplification 相关的网络例句 [注:此内容来源于网络,仅供参考]

A new LOS2 (Genbank accession no.: AY559080) gene was cloned from Capsella bursa-pastoris by rapid amplification of cDNA ends .

本研究在荠菜中克隆了一个新的冷相关基因转录调节因子Cblos2。

AY506804 gene from apsella bursa-pastoris by rapid amplification of cDNA ends . The full-length cDNA of Capsella bursa-pastoris ICE1 gene (Cbice53) including complete 5'-UTR and 3'-UTR was 1811bp long, containing a 1476bp open reading frame which encodes a 492 amino acids protein.

本研究在荠菜还得到了一个新的ICE1基因(基因bank登录号:AY506804),该基因(Cbice53)全长cDNA为1811bp,含有一个1476bp的开放阅读框,预测编码一个492个氨基酸的蛋白。

A new CBF (Genbank accession no.: AY391121) gene was cloned from Gapsella bursa-pastoris by rapid amplification of cDNA ends . The full-length cDNA of Capsella bursa-pastoris CBF gene was 1034bp long and contained a 657bp open reading frame encoding a putative DRE/CRT -binding protein of 219 amino acids.

本文克隆得到了荠菜Cbcor15b转录激活因子Cbcbf(基因bank登录号:AY391121)全长cDNA为1034bp,含有一个657bp的开放阅读框,预测编码一个219个氨基酸的DRE/CRT的结合蛋白质。

Objective:To examine the effects of ECRG2 in centrosome amplification and chromosome instability.

目的:非整倍体是肿瘤细胞的典型特征,是人类肿瘤染色体不稳定性的普遍形式。

Therefore, abnormal centrosome is common in tumor cells, and centrosome amplification is probably an early event in the origination and development of cancer.

因此,中心体异常也是肿瘤细胞的普遍特征,并且可能出现在肿瘤发生的早期阶段。

The activitys of Super Oxide Dismutase, peroxidase and Multiple Displacement Amplification of Ceratophyllum demersum L raised rapidly in the late of experiment, and the maximum value of MDA of Ceratophyllum demersum L in the eutrophic condition was 5 time higher than that in the medium nutritional condition, implied that Ceratophyllum demersum L has been stressed in the middle nutritional condition.

金鱼藻超氧歧化酶活性、过氧化物酶活性和丙二醛含量在试验后期上升速度加快,且富营养水平下金鱼藻MDA质量分数的最大值是中营养水平下最大值的5倍,表明在中营养水平下金鱼藻已经受到明显胁迫,而在富营养水平下受到胁迫更为显著。

A chalcone synthase gene was isolated from Ginkgo biloba leaves using the method of rapid amplification of the cDNA ends.

利用RACE技术克隆到银杏的一个查尔酮合成酶基因,命名为GbCHS2,其cDNA全长1608 bp,包括长1173 bp的读码框,编码391个氨基酸。

By mechanical inoculation, the in vitro transcripts of pUBF52 were infectious to Chenopodium amaranticolor, causing local lesions on the leaves same as that of wild type BBSV. Also, the virus amplification could be detected by Northern blot.

体外转录物摩擦接种表明,pUBF52的体外转录物对苋色藜具有侵染活性,可以在接种叶片上产生与野生型病毒接种相同的局部枯死斑点,同时可以在接种植物中检测到病毒RNA。

Salina by RT-PCR and 3¢ Rapid Amplification of cDNA Ends, which shared homology with Chlamydomonas (48%), Arabidopsis thaliana (50%), Homo sapiens (46%), etc.

序列分析显示克隆的cDNA全长1 650 bp,具有一定保守性,与衣藻、拟南芥和人的相似性分别为48%、50%和46%。

The major results of this proposal are as follows:(1) ABA induces a rapid, substantial accumulation of apoplastic H2O2 in mesophyll and bundle sheath cells of maize leaves, and the accumulation of apoplastic H2O2 is involved in the induction of the chloroplastic and cytosolic antioxidant enzymes.(2) ABA-induced H2O2 production activates a 46 kDa MAPK, which in turn induces the expression of antioxidant genes and up-regulates the activities of antioxidant enzymes. The activation of MAPK also enhances H2O2 production, forming a positive amplification loop.(3) Water stress also induces the activation of a 46 kDa MAPK, which is dependent on the accumulation of ABA and H2O2 production induced by water stress and involved in the up-regulation of the expression and the activities of antioxidant enzymes.(4) ABA-induced H2O2 production mediates NO generation, which in turn activates a 46 kDa MAPK and results in the up-regulation in the expression and the activities of antioxidant enzymes in ABA signaling. NO-independent signaling is also involved in ABA- and H2O2-induced antioxidant defense.

本项目的主要研究结果如下:(1)ABA诱导的H2O2产生主要出现在叶肉细胞与维管束鞘细胞的质外体中,质外体H2O2的积累能够上调叶绿体与细胞溶质中抗氧化酶的活性;(2)ABA诱导的H2O2产生活化一个46kDa的MAPK,由此而导致编码抗氧化防护酶基因的表达与酶活性的上调;而MAPK的活化也能增强H2O2的产生,从而形成一个正的反馈调节环;(3)水分胁迫也能诱导一46kDa MAPK活化,这一MAPK活化依赖于水分胁迫诱导的ABA积累以及H2O2的产生,同时参与水分胁迫诱导的抗氧化防护基因的表达与抗氧化酶活性的上调;(4)ABA诱导一个依赖于H2O2的NO产生,NO活化一个46kDa的MAPK,从而导致抗氧化防护基因的表达以及抗氧化酶活性的上调;同时一个不依赖于NO的信号转导途径也存在于ABA诱导的抗氧化防护过程中。

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