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- S1 gene hypervariable region I S1基因高变区I
- VP2 gene hypervariable region VP2基因高变区
- gene hypervariable region 基因高变区
- The gene cloning and sequence analysis of IBV S1 hypervariable region in Shandong 肾型IBV山东分离株S1高变区(HVR)的基因克隆与序列分析
- Cloning and Determination of S1 Gene of IBV GD05 Strain and Its Expression in E.coli. 与相似的文献。
- E2 protein, including hypervariable region 1 (HVR1) in the N-terminal region, contains some epitopes that can induce neutralizing antibodies. 包括高变区的E2蛋白含有中和性抗原表位,能诱导机体产生中和性抗体。
- The complete S1 gene from strain M41 of infectious bronchitis virus(IBV) was amplified by RT-PCR and cloned into the pGEM-T vector. 采用RT-PCR扩增出鸡传染性支气管炎病毒(IBV)M 41株的全长S1基因,并将其片段连接到pGEM-T载体,经酶切、PCR及序列测定表明,获得的S1基因ORF全长为1 659 bp,与G enB ank上公布的IBV M 41 S1基因序列一致。
- Using a reverse transcriptase polymerase chain reaction (RT-PCR) the 540bp-long S1 gene of two strains of avian Reovirus (ARV) (S1133,1733) were amplified successfully. 利用RT-PCR(Reverse Transcriptase-Polymerase chain Reaction)技术,扩增出禽呼肠孤病毒S1133、1733两毒株长为540bp的S1基因片段。
- Objective To clarify the significance of antibodies to hypervariable region 1(HVR 1) of hepatitis C virus (HCV) in chronic HCV-infected patients. 目的 探讨慢性丙型肝炎病毒 (HCV)感染者血清中抗高变区 1 (HVR1 )抗体的多型性及其临床意义。
- Objective:To acquire a series of high cross_reactive hypervariable region 1(HVR1) peptides of HCV isolated in China and their cocktail. 目的 :研究丙型肝炎病毒 (hepatitisCvirus ,HCV)第一高变区 (hypervariableregion 1,HVR1)抗原的交叉反应性 ,获得适合我国HCV感染株的高交叉反应性HVR1序列及其组合。
- Nucleotide similarities between the S1 gene of AVAV C-98 and that of ARV-176,MDRV-YJL,ARV-S1133 and ARV-138 were 99.9%,99.3%,97.9% and 81.2%,respectively. 与MDRV-YJL的同源性为99.;3%25;与弱毒疫苗株ARV-S1133的同源性也达97
- According to the published S1 gene sequence of ARV-S1133 strain in GeneBank,two pairs of primer were designed,one is sequencing primer,the other is diagnostic primer. 参考GeneBank中ARV-S1133株S1基因序列设计一对测序引物,一对诊断引物。
- Moreover, the viral genome of MW9710 strain could be amplified only with the primers specific for S1 gene of MDRV, but not with the primers specific for S1 gene of ARV by RT-PCR. 而以MDRV89026株S1基因的特异引物HP11、HP12进行RT PCR扩增,只能从MW9710等分离毒株中扩增出特异性条带。
- Aim To study the sequence diversity of the hypervariable region 1(HVR1) in the putative envelope protein E2/NS1 of genotype III/2a HCV in Chinese patients. 目的研究中国丙型肝炎患者III/2a型丙型肝炎病毒(HCV)包膜蛋白E2/NS1高变区1(HVR1)序列变异的规律及意义。
- Analysis of amino acids exhibited that the sequence of tested PRCV S1 gene is 100% homology with DQ811787 in Genbank, and 95.2% & 95.6% with M94096、M94097. 氨基酸推测分析表明,试验测序的PRCV S1基因氨基酸序列与Genebank中DQ811787同源性为100%25,与M94096、M94097的同源性分别为95.;2%25和95
- hypervariable region of VP2 gene VP2蛋白基因高变区
- A lot of point mutations were found in the S1 gene and N gene of the IBV isolates. In addition, a insertion mutation of 21-nt were found in the S1 gene of two IBV isolates, SC021202 and J. 在分离株的S1基因和N基因序列中均发现了大量散在的点突变,而且在SC021202株和J株的Sl基因中发现一段长21nt的插入片段,在以前的毒株中不存在。
- The extremely high variability of HCV especially at the hypervariable region of its envelope protein draws back the research to develop a vaccine against it in the traditional ways. 由于HCV具有不同的基因型,基因突变率高,尤其是包膜蛋白中的高变区,使得传统的疫苗制备方法在HCV面前显得束手无策。
- Total RNA of avian viral arthritis virus C-98 strain(AVAV C-98) isolated in Nei Monggol,China was extracted. According to the published S1 gene sequence of ARV-S1133 strain in GenBank,two pairs of primers were designed. 提取鸡病毒性关节炎病毒(AVAV)内蒙古分离株(C-98株)总RNA,参考GenBank中禽呼肠孤病毒(ARV)S1133株S1基因序列设计了2对引物,应用RT-PCR技术扩增了病毒S1基因,将S1基因cDNA克隆到pGEM-T Easy载体后测序。
- The invention discloses a hypervariable region 1 antigen in hepatitis C virus (HCV), and also discloses the purpose of the antigen in the preparation of hepatitis C virus detection reagent. 本发明公开了本发明提供丙型肝炎病毒(HCV)第一高变区抗原,还公开了该抗原在制备丙型肝炎病毒检测试剂中的用途。
