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1)  repeated and altered region of gD
gD基因重复高变区
2)  gene hypervariable region
基因高变区
1.
Sequence analysis of S1 gene hypervariable region Ⅰ of IBV strains isolated in Guangxi;
传染性支气管炎病毒广西分离株S1基因高变区Ⅰ的序列分析
3)  gD gene
gD基因
1.
Cloning and analysis of PRV-gD gene;
猪伪狂犬病病毒gD基因的克隆与分析
2.
Cloning and sequence analysis of gB,gC,gD genes of pseudorabies virus strain Fa;
伪狂犬病毒Fa株gB、gC、gD基因的克隆与序列分析
3.
Eukaryotic expression of gB, gC and gD genes of ILTV WG strain;
传染性喉气管炎病毒王岗株gB基因gC基因和gD基因的真核表达
4)  VH gene
重链可变区基因
1.
The VH gene ws amplified from genomic DNA of hybridomacells cells producing McAb against HBeAg byPCR reaction.
本文应用PCR技术从HBeAg单克隆抗体鼠─鼠杂交瘤细胞基因组DNA中扩增出重链可变区基因(VH),并将VH基因与pUC19载体连接,转化JM109菌,克隆出VH基因。
5)  S1 gene hypervariable region I
S1基因高变区Ⅰ
1.
The S1 gene hypervariable region I (HVR I) of 22 infectious bronchitis virus (IBV) strains isolated in Guangxi during the period of 1985-2007 were sequenced and compared to that of the other IBV reference strains and the pigeon coronavirus isolates.
对广西1985~2007年间分离到的22株传染性支气管炎病毒(IBV)的S1基因高变区Ⅰ(HVRⅠ)进行序列测定,并与发表的其他IBV参考株及鸽子分离的冠状病毒株的基因序列进行比较和分析。
2.
To investigate genetic variations of S1 gene hypervariable region I(HVR I) and nucleocapsid(N) protein genes and their variation correlation,S1 gene HVR I and N genes of 21 infectious bronchitis virus(IBV) strains isolated in Guangxi province of China between 1985 and 2008 were amplified by reverse transcriptase polymerase chain reaction(RT-PCR), cloned,sequenced and analyzed.
为了解广西传染性支气管炎病毒(IBV)的纤突蛋白S1基因高变区Ⅰ(HVRⅠ)和核(N)蛋白基因变异情况及S1和N基因变异间的相关性,本研究应用RT-PCR方法扩增了广西1985—2008年的21株IBV的S1基因HVRⅠ和N基因,并进行了克隆、序列测定及分析。
6)  VP2 gene hypervariable region
VP2基因高变区
1.
Based on the reported nucleotide sequence of IBDV in GenBank,a pair of primers that can amplify the cDNA of IBDV VP2 gene hypervariable region were designed.
参考GenBank发表的传染性法氏囊病病毒(IBDV)基因组序列,设计并合成了1对特异扩增IBDVVP2基因高变区的引物。
2.
According to the reported nucleotide sequence of IBDV in GeneBank,a pair of primers that can amplify the cDNA of IBDV VP2 gene hypervariable region were designed.
参考GeneBank发表的传染性法氏囊病病毒(IBDV)基因组序列,设计并合成了一对特异扩增IBDVVP2基因高变区的引物。
补充资料:重复基因
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性质:生物体中以串联方式重复排列在特定染色体上的某些多拷贝基因。如核糖体RNA基因、转移RNA基因和组蛋白基因都属于这类串联的多基因家族。

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