1) UL6 and UL7 gene
UL6和UL7基因
1.
To develop a SYBR GreenⅠreal-time quantitative PCR for detection of duck plague virus (DPV),specific primers were designed by using Beacon Designer software according to the UL6 and UL7 gene sequence available in GenBank.
根据GenBank中鸭瘟病毒(DPV)UL6和UL7基因的保守序列,设计了一对特异性引物,扩增位于UL6和UL7基因第891～991位长度为101bp片断。
2) UL6 gene
UL6基因
1.
Prediction of epitopes on B cell of UL6 gene of duck enteritis virus and prokaryotic expression of major antigen determinant sequence;
鸭肠炎病毒UL6基因B细胞表位的预测及其主要抗原域的原核表达
2.
To identify the features of DEV UL6,the "targeted gene walking PCR" was used to amplify the UL6 open reading frame(ORF) of the DEV Clone-03,and a 2,534 bp DNA fragment was obtained,which covers the entire DEV UL6 gene of the DEV Clone-03 genome.
为了研究鸭肠炎病毒(Duck enteritis virus,DEV)UL6的特征,以DEV Clone-03株基因组DNA为模板,用靶基因步移PCR方法扩增得到UL6基因区域2534 bp的DNA片段。
3.
In this study,the UL6 gene of pseudorabies virus(PRV) strain Ea was amplified by PCR and cloned into pMDI8-T vector.
根据测定的序列,设计一对能扩增UL6基因完整编码区的引物,PCR扩增UL6基因并将其插入真核表达载体pEGFP-C2中EGFP基因的3′端,获得与EGFP融合表达的真核表达质粒pEGFP-UL6,转染Hela细胞,通过激光共聚焦显微镜观察发现,转染48 h,融合蛋白EGFP-UL6主要定位在胞浆,为进一步研究伪狂犬病病毒Ea株UL6基因的结构和功能奠定了基础。
3) UL1-UL7 gene
UL1～UL7基因
5) P20 and P14 gene
P20基因和P14基因
补充资料：J基因
分子式：
CAS号：
性质： 为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。
CAS号：
性质： 为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条