查询词典 transcription

CRM genome screeners screen sequences or complete genomes for CRMs as homotypic or heterotypic clusters of binding sites for any combination of transcription factors.

CRM基因组筛选器作为任何组合的转录因子的同型的或异型的结合位点类为CRMs筛选序列或全部基因组。

The protein products of Hox genes,as transcription factors,are also highly conserved.

Hox基因是存在于染色体上的一段高度保守序列，其蛋白产物作为转录因子也是高度保守的。

Characterization of MYB and HOX transcription factors involved in controlling cotton fiber development

单萜、倍半萜及挥发性成分的生物合成及调控网络；控制棉纤维发育的MYB 和HOX 转

hyperglycemic rats;insulin intensive therapy; scald and trauma; nuclear transcription factor-κB; liver

j Qkko0 高血糖大鼠；胰岛素强化治疗；烫伤和创伤；核转录因子κB；肝脏

In order to improve the viral detection method in shrimp, a more rapid and convenient multiplex reverse transcription-polymerase chain reaction was established in the present study. The new method was used for detection of shrimp viruses, including Yellow-head virus, white spot syndrome virus, Taura syndrome virus, hepatopancreatic parvovirus, infectious hypodermal and hematopoietic necrosis virus and monodon baculovirus.

为了提高对虾病毒检测的快速性和简便性，建立了一种可同时检测6种对虾病毒的RT-PCR方法，并利用该方法对来自广西沿海地区的130份病虾样品中的黄头病毒、白斑综合征病毒、桃拉病毒、肝胰腺坏死病毒、传染性皮下组织坏死病毒以及杆状病毒进行了检测。

The object of this study is looking for the salt-toierancc re I atcd gcncs lroiit the hatiophy Lu l. imonium SIUCIWC 0. Kuntze. By using of the technique of liffcrential Display RT-PCR DDRT-PCR, the di lfercntiai expressIon pattern betwecn salt\' treated plant and thc control were anaii.zecl.

本实验设计目的是寻找有价值的耐盐相关基因，利用DDRT-PCR（Differential Display Reverse Transcription-Polymerase ChainReaction， mRNA差别显示）技术对补血草Limonium sinense O。

Methods Reverse transcription polymerase chain reaction method was adopted in detecting VEGF-CmRNA expression in 60 cases of breast infiltrative tubular cancer.

方法用逆转录聚合酶链反应法检测60例乳腺浸润性导管癌VEGF-C mRNA的表达情况，取15例乳腺纤维腺瘤标本作为对照。

MAIN OUTCOME MEASURES: At three and six weeks after injury, the infraspinatus were harvested to detect EGF, PDGF, TGF-β and BFGF by reverse transcription-polymerase chain reaction.

主要观察指标：术后3周，6周取岗下肌腱标本RT-PCR检测表皮生长因子、血小板源性生长因子、转化生长因子β、碱性成纤维细胞生长因子表达水平。

It encodes a putative zinc finger transcription factor, and is a transcriptional corepressor for thyroid hormone receptors. Hairless gene plays a critical role in maintaining the delicate balance between cell proliferation, differentiation, and apoptosis in the hair follicle as well as in the interfollicular epidermis, and is concerned with the control of hair growth cycling.

无毛基因是与皮肤和被毛结构有重要关联的核受体基因，编码一个锌指结构转录因子，是甲状腺激素受体的转录辅阻遏物，并参与毛发生长周期的调控，在维持毛囊及毛囊间上皮的增殖、分化、调亡的精致平衡中扮演重要角色。

Gondii, were cloned by PCR respectively. The PCR products were digested by the corresponding enzymes and ligatd into the intermedial vectors. Finally, the inducible RNAi vector, pBSK-HSP70/5UTR-IntronC-HSP70/3UTR, with the HSP70 gene promotor as a promotor, the intron C sequence ofβ-tubulin gene as intervening sequence, 3UTR sequences of HSP70 gene as transcription stop signals, was constructed successfully, and the results of sequencing were correct. 3The construction of the inherited and inducible RNAi vector system of T. gondii: The fragment of SAG1/5UTR-eGFP-SAG1/3UTR in pBSK-SAG1/GFP vector was cloned into the vector of pBSK-HSP70/5UTR-IntronC-HSP70/3UTR to construct pBSK-GFP-Hairpin vector, then the fragment of GFP-Hairpin in pBSK-GFP-Hairpin vector was cloned into pHANA-0.5 vector.

弓形虫可诱导的反向重复序列RNAi载体的构建：设计引物，通过PCR分别扩增弓形虫HSP70基因5&UTR启动子序列(HSP70／5UTR)、HSP70基因3&UTR序列(HSP70／3UTR)及β-微管蛋白基因内含子C序列，通过酶切连接，构建以弓形虫热休克蛋白HSP70基因启动子进行驱动的，以β-微管蛋白基因内含子C序列作为间隔序列，以HSP70基因3UTR序列作为转录终止信号的反向重复序列RNAi载体pBSK-HSP70／5UTR-IntronC-HSP70／3UTR，序列测定结果正确。

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。