hexon

After a pair of primers for hexon gene were designed , the PCR was carried out and the immuno-PCR assay technique was therefore established through the quantitative analysis of the amount of amplified DNA fragments instead of the enzyme-substrate reaction of ELISA .

设计一对扩增六邻体基因的引物进行PCR，通过对DNA扩增片段浓度的定量分析，替代ELISA方法中的酶-底物显色反应而建立TNF-α的免疫PCR检测方法。

Construction and expressing of Hexon gene of human adenovirus type 3

人3型腺病毒六邻体基因表达质粒的构建及表达

Homology Modeling and Evolution Trace Analysis of Human Adenovirus Type 3 Hexon

人3型腺病毒六邻体蛋白同源建模及其进化轨迹分析

Methods Under the optimum expression conditions , the hexon protein of human type 3 adenovirus was efficiently expressed in E.

方法在原核表达系统中高效表达重组人3型腺病毒六邻体蛋白。

Purification and antigenicity detection of recombinant hexon of human type-3 adenovirus

重组人3型腺病毒六邻体蛋白纯化及抗原性检测

The template was amplified by the primers of adenovirus hexon gene .

用腺病毒六邻体基因的特异引物扩增指标分子。

Cloning of Hexon-encoding Gene of Egg Drop Syndrome Virus and Construction of Eukaryotic Expression Plasmids of Hexon Gene

减蛋综合征病毒六邻体蛋白基因的克隆与真核表达载体的构建

Objective To purify the recombinant hexon of human type-3 adenovirus and detect its antigenicity .

目的纯化重组人3型腺病毒六邻体蛋白并检测其抗原性。

Analysing the sequence of hexon of adenovirus type 3 epidemiced in 2004 in Guangzhou

2004年广州地区流行的3型腺病毒六邻体基因序列分析

With a sequence from the Genebank that includes part of hexon gene , DNA binding protein gene and the whole protease gene , two pairs of oligonucleotide primer sets were designed by using PRIMER program and synthesized .

从GeneBank的1段含六邻体蛋白基因、蛋白酶基因、DNA结合蛋白基因的序列中，应用Primer软件设计了2对引物。

Aim To analyze conserved region amino acid sequences of human adenovirus ( HAdV ) hexon , and to synthesize conserved peptides and prepare anti-peptide antibodies , then to determine intertype-specific epitopes .

目的分析人类腺病毒（HAdV）六邻体保守区氨基酸序列，合成保守区多肽并制备抗多肽抗体，以确定型间共同的特异性表位。