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猪瘟兔化弱毒的英文

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"猪瘟兔化弱毒"怎么读用"猪瘟兔化弱毒"造句

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  • hclv

例句与用法

  • Studies on enhaning effect of alfalfa polysaccharide on the immune response of lapinized chinese strain of classical swine fever virus
    苜蓿多糖对猪瘟兔化弱毒疫苗免疫应答强化作用的研究
  • The sows , which are not pregnant , are vaccinated by hcv vaccine of different dose and then detected antibody against hcv with ppa - elisa at different time
    给空怀母猪接种不同剂量的猪瘟兔化弱毒疫苗,分别于不同时期用ppa - elisa检测血清抗体。
  • Hc ( hog cholera ) , the virulent infectious disease caused by hcv ( hog cholera virus ) , had been controlled effectively by hclv strain vaccine in the country
    猪瘟是由猪瘟病毒引起的猪的一种病毒性传染病。猪瘟兔化弱毒疫苗有效地控制了猪瘟在我国的急性发生和大流行。
  • Successfully cloned and constructed infectious full - length cdna of attenuated lapinized csfv chinese - strain ( derived from spleen ) could make us get pure rna virus genome of csfv c - strain , and further study and utilize mutation , deletion , insertion and substitution of csfv gene on dna molecular level
    中国猪瘟兔化弱毒(脾淋毒)全长感染性cdna的克隆和构建,可以使我们得到纯粹的csfvc -株rna病毒基因组,在dna水平上研究和利用csfv的基因突变、缺失、插入和替换。
  • A pair of primers were chemically synthesized based on the cdna sequence of hog cholera virus strain brescia and used to amplify the cdna fragments of envelope glycoprotein e2 gene of hclv which coding the major protective antigen by reverse transcription - polymerase chain reaction ( rt - pcr ) from total intact rna extracted from infected calf testicle cell culture by hclv
    猪瘟兔化弱毒犊牛睾丸细胞毒( hclv )中提取的细胞总rna为模板,以rt - pcr技术,扩增出了完整e2基因的cdna片段。经电泳、酶切分析,证实了所扩增片段为e2基因特异性片段。
  • The expression conditions of e2 gene in p . pastoris were optimized , the results indicated that the peak obtained after 72 hours ; pattern of inhibition / induction could improve expression level ; the best ph value were between 7 . 5 and 8 . 0 and the optimized methanol - induced concentration was 2 % - 3 % the e2 genes of the prevalent strain ( guangxi yulin strain ) and c strain derived from rabbit spleen tissue were amplified and cloned into e . coli the expression vector pproex - htb respectively , the recombinant plasmids pproex - gxyl and pproex - c were obtained and then were transformed into the dh5a e . coli competent bacteria respectively , the recombinant bacteria could express the major antigen region of e2 gene , the expression yields amount to 35 % and 38 % repectively
    猪瘟病毒ez基因的原核表达: pcr扩增出当前猪瘟流行野毒株,中国猪瘟兔化弱毒( c株)兔脾组织毒ez基因的主要抗原区,将其克隆到原核大肠杆菌表达载体pproex htb中诱导表达,经sds page检测表明,重组质粒能表达ez基因主要区蛋白, westernblot检测表明,诱导表达蛋白与猪瘟阳性血清发生特异性反应,表达量为35和38 ,可用于基因工程诊断抗原。
  • The study is mainly about finding the reason that caused atypical hc through analysis and homology comparison on e2 gene sequences and amino acid sequences of e2 glycoprotein among strains hclv , fc , hcv - jn , hcv - yc , shimen et . al . at last , the best program against hc was established in order to control and erase hc
    本研究主要是对猪瘟兔化弱毒疫苗、猪瘟病毒野毒株抗原基因( e2 )进行序列分析和同源性比较,分析发生非典型性猪瘟的原因,并在此基础上制定最佳猪瘟免疫程序。
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