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鹅细小病毒的英文

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"鹅细小病毒"怎么读用"鹅细小病毒"造句

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  • goose parvovirus

例句与用法

  • Goose parvovirus ( gpv ) is the pathogen of goslings plague
    鹅细小病毒( gooseparvovirus , gpv )为小鹅瘟的病原体。
  • Goose provirus ( gpv ) is the pathogen of highly contagious and fatal infectious diseases of goslings and muscovy ducklings
    鹅细小病毒( gooseprovirus , gpv )可引起雏鹅、雏番鸭高度致死性传染病?小鹅瘟。
  • Vp2 is one of viral structural proteins on the surface of provirus . its neutralizing antigenicity has been proved . in this study
    Vp2是鹅细小病毒结构蛋白之一,是gpv的重要保护性抗原,在体内诱导的抗体具有中和作用。
  • Goose parvovirus is the causitive agent of goose plague . which is also named as derzsy ' s disease . it is one of highly fatal diseases of goslings and muscovy ducklings
    鹅细小病毒( gooseparvovirus , gpv )主要引起雏鹅、雏番鸭的高致死性疾病,称为小鹅瘟或derzsy ' s病。
  • This study provides the basis evidence for the research of nucleotide sequence evolution relationship between domestic and exterior countries . it also establishes foundation for further research about developing gpv molecular diagnostic reagent and genetic engineering vaccine
    本研究为了解国内外鹅细小病毒核苷酸序列演化上的关系,为开发研制新型分子诊断试剂和抗鹅细小病毒感染的基因工程疫苗提供了理论依据。
  • The pathogen of goose plaque , goose parvovirus ( gpv ) , can cause acute infectious disease characterized by acute intestitis and inflammation of liver , kidney and heart in goslings and muscovy duckings under 1 month of age , which threaten the goose industry
    鹅细小病毒( gooseparvovirus , gpv )为小鹅瘟的病原体。小鹅瘟主要发生于1月龄内雏鹅和雏番鸭,是以急性肠炎及肝、肾、心实质脏器炎症为特征的烈性传染病,对养鹅业发展造成很大威胁。
  • In this study , the recombinant fowl - poxvirus was transfected into expressing the vp3 gene of isolated gpv h1 strain into the cef cells with fpv - 017 by liposome , which have the lacz reporter gene , earlier / latter promoters lp2ep2 of fpv , promoters p7 . 5 and p7 . 1 of vaccinia virus , replication unnecessary region of fpv - 017 . following 6 cycles screenings , clonings , purification of blue plaques , detection of pcr and dot - elisa , which verified the genetic stable vp3 - fowlpox virus recombinant constructed successfully . this study provided the theoretical and practical foundation for development of gpv recombinant fowl - poxvirus genetic engineering vaccine , as well as provided substance preparatory for prevention the high mortality gpv
    本研究采用脂质体转染方法,将含有完整gpvh1分离株vp3基因、报告基因lacz 、禽痘病毒早晚期启动子lp2ep2 、痘苗病毒启动子p7 . 5 、 p11和fpv - 017复制非必须区的转移载体质粒psy681vp3lacz与fpv - 017共转染鸡胚成纤维细胞,经6轮蚀斑克隆、筛选、表达, pcr鉴定和dot - elisa检测,证明该重组病毒已构建成功,并获得了遗传性状稳定的鹅细小病毒vp3基因的重组禽痘病毒。
  • The recombinant plasmid was identit1ed with restriction endonuclease , pcr , then sequenced . the resuit of sequence analysis showed that the vp3 gene is 1605bp and inc1uds a complete open reading frame encoding a protein of 534 amino acids . the hl isolate shares 98 . 5 % and 98 . 3 % identity with b isolate at nucieotide and amino acid levels respectively
    结果表明:鹅细小病毒h1分离株vp3基因全长1605bp ,编码534个氨基酸,只有一个完整的开放阅读框架,与国外已发表的鹅细小病毒b株核苷酸序列同源性为98 . 5 ,氨基酸序列同源性为98 . 3 ,表明这二个毒株亲缘关系相近。
  • The close genetic relationship of goose parvoviruse and aav allows the examination of the molecular biological properties of the nonstructural proteins of gpv . after the gpv infected the cell the viral life cycle was regulated by the nonstructural proteins encoded by the virus . according to the published of gpv b strain genome nucleotide sequences in genbank and a pair of specific primers were disigned with oligo4 . 1
    本研究根据genbank发表的gpvb株全基因序列,借助oligo4 . 1软件设计一对引物,采用pcr技术扩增gpvh1株非结构蛋白ns2基因,并与pmd18 - t载体连接后测序,结果表明:鹅细小病毒h1株ns2基因核苷酸全长1356bp ,编码451个氨基酸残基,与gpvb株的ns2基因相比,核苷酸数目相同,有17个碱基、 6个氨基酸的差异;同源性分析表明:二者核苷酸序列同源性为98 . 75 ,推导氨基酸序列同源性为98 . 67 。
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