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1)  VP2 variable region
VP2可变区
1.
Using RT - PCR technique, the cDNA fragments with length of 454 bp of VP2 variable region were amplified.
VP2可变区个别氨基酸的改变可引起毒力和抗原性改变,但不是唯一的决定因素。
2)  VP2 hydrophilic region
VP2高变区
3)  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。
4)  VP2 hypervariable region
VP2基因高变区
1.
The VP2 hypervariable regions(vVP2)were amplified by RT-PCR/Nest.
应用Nested-PCR分别对3株分离株VP2基因高变区进行克隆测序和序列分析,结果表明:3个分离株与国内外参考超强毒株的核苷酸同源性为97。
5)  hypervariable region of VP2
VP2基因高变区
1.
RT-PCR based on a set of primers designed to amplify the hypervariable region of VP2 gene(vVP2) of infectious bursal disease virus(IBDV) was used to detect the tissue samples of Fabricus\' bursa collected from a clinical flock in Yongzhou region of Hunan province.
设计针对传染性法氏囊病病毒(IBDV)VP2基因高变区(vVP2)的引物对湖南永州送检的一群疑似传染性法氏囊病病例的法氏囊组织通过逆转录-聚合酶链式反应(RT-PCR)技术进行检测,应用鸡胚绒毛尿囊膜(CAM)接种的方法对阳性样品进行病毒分离,同时对IBDV分离株中的vVP2进行限制性内切酶分析和核苷酸序列测定,分析关键位点的氨基酸特征和同源性,绘制遗传进化树。
6)  hypervariable region of VP2 gene
VP2蛋白基因高变区
1.
Specific PCR primers for hypervariable region of VP2 gene(vVP2) of infectious bursal disease virus(IBDV) and hexon gene of fowl adenovirus(FAV)were designed respectively to detect the genomes of IBDV and FAV from bursal and cloacal swab samples of two individual birds in a flock in which an outbreak of IBD was clinically suspected.
应用设计的分别针对传染性腔上囊病病毒(IBDV)VP2蛋白基因高变区(vVP2)和Ⅰ群禽腺病毒(FAV)六邻体(hexon)蛋白基因的特异性PCR引物,对临床疑似IBD病例的2只鸡的腔上囊样品和泄殖腔拭子样品分别进行IBDV和FAV的分子检测。
补充资料:可变区基因
分子式:
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性质:又称V基因。指编码抗体可变区的基因。现可用重组技术将两个不同的可变区基因组建在一个抗体编码区中,从而可表达出具两种抗体性能的双效抗体。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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