1、

TRAP α was a glycosylated protein with the weight of 34 kD in mammal, which was under regulation of Ca2+ and located in the endoplasmic reticulum and nuclear envelope.

哺乳动物TRAPα是一个糖基化蛋白,大小为34kD,它受到Ca2+的调控,分布在内质网膜和核膜。

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2、

Prediction of B cell epitope in B domain of envelope E protein of Chinese dengue 2 virus

我国登革2型病毒包膜E蛋白B区抗原表位的预测

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3、

P32 protein is one of the virus structure proteins. It stands out on the virus envelope surface and contains neutralized antigen epitope.

羊痘病毒P32蛋白是位于羊痘病毒膜表面的主要结构蛋白,含有中和抗原表位;

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4、

Hemagglutinin-neuraminidase as a fiber protein on NDV envelope has the absorption function to host cells.

血凝素-神经氨酸酶(Hemagglutinin-neuraminidase,HN)作为NDV包膜上的纤突,具有吸附宿主细胞的功能。

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Results Fifty of the 1929 ANA positive cases detected ANA were positive for anti-nuclear envelope protein autoantibodies.

结果1929例血清标本中50例抗核包膜蛋白抗体阳性,相关疾病包括PBC等多种系统性自身免疫病。

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The obtained polyclonal antibody against domain ⅲ of envelope protein has some specificity; 4.

收获的抗登革病毒E蛋白第三结构域多克隆抗体具有一定的反应特异性;4。

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7、

Immunogenicity and antigenicity of Japanese encephalitis virus envelope protein domain ⅲ

日本脑炎病毒SA14-14-2E蛋白结构域Ⅲ的抗原性和免疫原性分析

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8、

Because of these deletion mutations, functional envelope protein could not be produced. S gene and HBV DNA polymerase gene are completely overlaps, but these variants were still predominant with mutated polymerase. The mechanism and significance were worth in-depth study.

由于复杂突变的变异株不能产生功能性包膜蛋白,S基因与HBV dna聚合酶基因完全重叠,而这类变异株为优势毒株,其机制和意义值得深入研究。

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Methods: The putative envelope protein 2 gene fragments of HCV in sera from Shandong ( SD), Shanghai ( SH) patients were amplified by reverse transcription nested PCR and sequenced.

方法:对来自山东(SD)、上海(SH)两地患者血清RNA进行逆转录-巢式PCR,扩增HCV囊膜蛋白2基因片段,用PCR直接测序法对该片段进行序列测定。

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10、

study on dna immune of envelope protein gene of rift valley fever virus

裂谷热病毒囊膜蛋白基因DNA免疫的研究

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11、

we analyze the hepatitis c virus ( hcv) envelope protein-coding sequences from 18 general geno/ subtypes worldwide, and find 4 amino acid sites under positive selection.

我们应用最大似然法分析了丙型肝炎病毒的包膜蛋白编码序列,从全世界18个常见的基因型/亚型中,发现了4个正选择/适应性位点。

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12、

Cloning and sequencing of major envelope protein and membrane protein genes of equine arteritis virus

马动脉炎病毒大囊膜蛋白和膜蛋白基因的克隆与序列分析

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13、

42K envelope protein gene of Contagious Ecthyma virus were amplified by specification primers and recombinant to different expression vector. The 9 strains stable recombinant were screened by dot blotting and southern blotting with DNA probe labeled DIG.

用特异性引物扩增羊传染性脓疱病毒42K囊膜蛋白基因,与不同的表达载体重组后用DIG标记的特异性DNA探针进行Dot-blotting和southern blotting杂交检测,挑选出能稳定传代的重组菌9株。

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14、

The cloning and expression of contagious Ecthyma virus 42K envelope protein gene

羊传染性脓疱病毒42K囊膜蛋白基因克隆及表达

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15、

Influence of Intramolecular Disulfide Bond on Fusion Core Structure of Envelope Protein of HERV

分子内二硫键对HERV囊膜蛋白融合核心结构的影响

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16、

Retroviral Vector Mediated CSFV E2 Envelope Protein Gene Expression in Eukaryotic Cells and Animal Immune Experiment

逆转录病毒载体介导的猪瘟病毒E2基因在真核细胞中表达及动物免疫试验初报

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17、

Using the recombinant envelope protein of WNV as antigen, the serum antibody was detected by ELISA.

方法利用构建的包膜蛋白重组质粒(pQE-30)表达纯化西尼罗病毒包膜蛋白,以此为抗原进行ELISA检测。

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