查询词典 gene library

In different embryo developmental stages, its expression was decline gradually . This result indicated that the survivin may play important role in oogenesis and early embryogenesis. One PABP gene was cloned from the subtractive cDNA library.

RT-PCR分析表明该基因主要在卵巢中表达，随着胚胎发育表达逐渐减少，这可能表明该基因在半滑舌鳎卵子形成和早期胚胎发育中起到重要作用。ePABP是特异的在卵巢和早期胚胎表达的Poly结合蛋白。

Based on the established library,an antibacterial peptide gene was obtained primely using PCR method.

利用建立的宏基因组文库，采用PCR技术初步筛选到具有编码抗菌肽的功能基因。

By screening a rice genomic library, we isolated a TB1-like gene-Oryza sativa Teosinte Branched (OsTB1) in rice. We also isolated the cDNA of OsTB1 by RT-PCR.

通过筛选水稻的基因组文库，得到了水稻中的一个TB1同源基因Oryza sativa Teosinte Branched1 (OsTB1)。

In this paper, we studied M. meretrix ferritin, cathepsin B and caspase genes, which are involved in clam larval shell formation, nutrition, metabolism and apoptosis, respectively. We have cloned the three genes, investigated the temporal and spatial expression profile both at gene and protein level in trochophore (L1), D-veliger (L2), pediveliger (L3) and postlarvae (L4). The potential roles of these proteins were analyzed with specific inhibitors during larval development. Firstly, embryos were found developed into trochophore-like larvae with no shell if cultured at gastrula stage in artificial seawater without iron. Shell-like structures were formed only in the presence of iron. The larvae which had been transferred at L1 stage into ASW developed normal shell. This indicated that iron and iron associated protein are important for larval shell formation. The EST sequence which is homologous with ferritin, which is a principal iron metabolic protein, was selected from the M. meretrix cDNA library. The full-length of ferritin subunit cDNA was cloned by RACE. The results of real-time PCR revealed that the MmeFer mRNA expression changed before and after the larval shell formation.

本论文以文蛤幼虫为研究对象，分别对文蛤幼虫发育过程中贝壳形成相关的铁蛋白、营养及变态相关的组织蛋白酶B及变态过程中细胞凋亡相关的caspase三个基因进行了克隆，分析了基因及编码蛋白在担轮幼虫期(L1)、D形幼虫期(L2)、壳顶幼虫期(L3)和稚贝期(L4)的时空表达特征，解析了其可能的功能，并研究了相应酶类的特异性抑制剂作用对幼虫发育过程的影响，进行了目标蛋白的功能验证，详述如下：研究结果显示，在文蛤胚胎发育到原肠胚时放入不含铁离子的人工海水中培养，发育成无壳的畸形，随着人工海水中铁离子添加浓度的升高，幼虫长出壳状组织接近正常状态；而发育到L1期幼虫放入不含铁离子的人工海水中培养却可以发育出正常的壳，推测铁和铁代谢相关蛋白在幼虫贝壳初始形成有重要的作用。

To understand whether the GST can protect plant from the damage of ultra-violet radiation,a UV inducible GST gene was isolated from an Arabidopsis cDNA library.The plant expression vector containing the GST cDNA was constructed and transferred into Arabidopsis thaliana plants by the Agrobacterium-mediated vacuum method.Molecular genetic analyses showed that the overexpression of the UV inducible GST could increase the tolerance of the transgenic plants to UV radiation

为了阐明GST在紫外辐射下是否对植物有保护作用，以紫外强烈诱导表达的GST cDNA为探针，筛选拟南芥cDNA文库，获得了这种GST的全长cDNA；利用此cDNA构建植物表达载体，并通过农杆菌介导法转化拟南芥，使其在拟南芥中得到大量表达；通过对转基因植株的紫外辐射耐性分析，证实了该GST的过量表达可明显增强拟南芥对紫外辐射损伤作用的耐受性。

In order to clone AVR-Pia, the flanking sequence of MS220K4 was used as a probe to screening the TAC library and 17 positive clones were obtained. Further restriction enzyme mapping and Southern blot analysis on 10 of the 17 positives clones narrowed the avirulence gene to a region of 10 kb.

为克隆AVR-Pia基因，以MS220K4的侧端序列为探针筛选稻瘟菌基因组TAC文库，得到17个阳性克隆，通过对其中10个进行的限制性内切酶分析并结合Southern杂交确定了目的基因所在区域。

The mouse embryonic stem cells cDNA library was screened by yeast two-hybrid assay,some candidate molecules were get,including DDX39 DEAD (Asp-Glu-Ala-Asp box polypeptide 39, BAT1A(HLA-B-associated transcript 1A), NAC1 ( nucleus accumbens-1 ), BicD2 (bicaudal D homolog 2)、MLL3 (myeloid/lymphoid or mixed-lineage leukemia 3). NAC1 and MLL3 were associated with regulation of gene transcription. DDX39 andBAT1A were associated with pre-mRNA processing and mRNA export from nucleus to cytoplasm. BicD2 was associated with the regulation of Golgi body.

通过利用酵母双杂交方法，以小鼠全长Plk1作为诱饵蛋白筛选小鼠胚胎干细胞cDNA文库中与其相互作用的蛋白，获得了DDX39DEAD(Asp-Glu-Ala-Aspbox polypeptide 39、BAT1A(HLA-B-associated transcript 1A)、NAC1(nucleus accumbens-1)、BicD2(bicaudal D homolog 2)、MLL3(myeloid／lymphoid or mixed-lineage leukemia 3)等几个候选蛋白，其中NAC1、MLL3与基因的转录调控有关，DDX39、BAT1A与mRNA前体的剪切、加工及mRNA从细胞核转运到细胞质紧密相关，而BicD2与高尔基体的调控紧密相关，提示我们Plk1与基因转录、mRNA前体的剪切、加工、mRNA的运输及胞质分裂中高尔基体的调控有关。

Methods The BiVP gene was screened by the ESTs technology and cloned by PCR method from the cDNA library of the bumblebee, Bombus ignitus. It was reconstructed to form the baculovirus transfervector pBac1-BiVP and expressed in Sf-9 insect cell. The recombinant BiVP was purified by the fast protein liquid chromatography system.

利用ESTs从红光熊蜂cDNA文库中获得BiVP基因，以PCR技术扩增出BiVP的完整cDNA，并构建病毒表达载体PBac1-BiVP，通过昆虫杆状病毒表达系统，在Sf-9昆虫细胞中进行表达，表达产物用快速蛋白液相色谱系统进行纯化。

This high quality cDNA library can be further used for gene clone and ESTs analysis and provides a useful tool for the study of the molecular mechanisms of winter-blooming of Chimonanthus praecox.

LTP基因在蜡梅开花过程中可能具有重要的生物学功能，为探索蜡梅冬季开花分子机理提供了线索。

Objective Screening ,molecular cloning , and identifying of encoding gene of fibrinolytic activity protein from cDNA library established from clamworm digestive tract epithelial cells by SMART(Switching Mechanism At 5' end of the RNA Transcript) technology .

①目的：构建沙蚕消化道上皮细胞的cDNA文库，并从中筛选、克隆和鉴定一种具有纤溶活性的蛋白编码基因序列。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。