为了进一步检测转基因大米的抗病毒性能，研究小组准备首先比较大米和由玉竹提炼而来的纯抗病毒蛋白质的抗病毒性能。
To test the effect further, they plan to compare the antiviral powers of the GM rice that has produced the protein with protein isolated directly from Yuzhu.
但是这种蛋白质的“头”的结构很容易发生变异，当它改变形式时允许病毒不被检测到。
But the structure of the protein's "head" mutates readily, allowing the virus to go undetected when it changes form.
间接免疫荧光、ELISA和免疫印迹检测证明，含SO.7片段的三种重组杆状病毒均在昆虫细胞中表达出相应的活性蛋白。
By IFA, ELISA and Western blot experiments, it was proved all the recombinant baculoviruses containing SO. 7 segment could express biologically active proteins in insect cells.
用亲和层析纯化的猪繁殖与呼吸综合征病毒(PRRSV)重组核衣壳蛋白gst - N作为诊断抗原，建立检测prrs血清抗体的间接ELISA方法。
Using recombinant nucleocapsid protein GST-N of porcine reproductive and respiratory syndrome virus (PRRSV) as antigen, an indirect ELISA for the detection of antibodies against PRRSV was developed.
目的：建立高灵敏检测蓝舌病毒VP7蛋白的生物条形码检测方法。
Objective: to establish a high sensitive bio-bar codes assay method for detecting bluetongue virus (BTV) VP7 protein.
试剂盒采用原核表达的重组P30蛋白作为包被抗原，依据竞争ELISA原理检测猪血清中非洲猪瘟病毒的抗体。
The kit adopts prokaryotic expression recombinant P30 protein as coating antigen, and detects the African swine fever virus antibody in pig serum according to a competitive ELISA principle.
本文以藻红蛋白为荧光探针，探讨了藻红蛋白荧光标记技术及荧光探针在烟草花叶病毒免疫检测中的应用效果。
The fluorescence labeling technique of phycoerythrin and application for the immunoassay of Tobacco mosaic Virus were studied in this research using it as a labeling probe.
所以事实上他们所作的是检测构成以前大流行病毒株基因表达的蛋白的成分并且寻找这些病毒株间交叉的重复模式。
So in effect what they did was scan all the building blocks of proteins that all the genes of previous pandemic strains expressed and looked for repeated patterns across the strains.
原核表达并纯化单纯疱疹病毒特异性糖蛋白抗原，用于建立单纯疱疹病毒的临床检测方法。
To express and purify the specific glycoprotein antigens of herpes simplex virus (HSV) as used in HSV clinical detection.
用表达的口蹄疫3a蛋白作为包被抗原，建立了间接elisa试验，对口蹄疫病毒感染血清、免疫血清和其它非口蹄疫病毒血清进行了检测研究。
An indirect ELISA was established with expressed 3a protein of FMDV as coating antigen and was experimentally used to detect FMDV infection sera, immune sera and other disease sera.
间接免疫荧光检测到病毒蛋白的表达。
The protein expression of chimeric virus was identified by indirect immunofluorescence analysis.
目的建立原材料胰蛋白酶中猪细小病毒的PCR检测方法。
Objective To establish PCR assay of Porcine Parvovirus detection in Trypsin.
旨在建立一种检测口蹄疫病毒非结构蛋白抗体的敏感、特异的ELISA方法。
To develop a sensitive and specific ELISA for detection of antibodies to the nonstructural protein of FMDV.
重点讨论了各种检测方法在实际中的应用，百合无症病毒提取过程中需要解决的问题，外壳蛋白基因在大肠杆菌中表达载体的构建。
The discussion was mainly focused on the application of these detection methods, the problem result in the virus extraction progress, and the construction of expression plasmid having LSV CP gene.
目的检测犬贾第虫病毒介导的锤头状核酶对犬贾第虫滋养体核仁功能性蛋白krr1基因体外转录体切割效率。
Objective to detect the cleavage activity of Giardia Canis virus (GCV) transfer vector-mediated hammerhead ribozyme for KRR1 in vitro transcript.
为了进一步检测转基因大米的抗病毒性能，研究小组准备首先比较大米和由玉竹提炼而来的纯抗病毒蛋白质的抗病毒性能。
To test the effect further, they plan to compare theantiviralpowers of the GM rice that has produced the protein withproteinisolated directly from Yuzhu.
本文建立了一种用于检测猪乳中抗轮状病毒免疫球蛋白A的ELISA方法。
An enzyme-linked immunosorbent assay (ELISA) method was developed to allow direct quantification of antirotavirus immunoglobulin A (IgA) in sow colostrum and milk.
目的制备诺如病毒衣壳蛋白特异性单克隆抗体，为诺如病毒的快速检测及致病机制的研究提供实验材料。
To prepare the monoclonal antibodies against Norovirus capsid protein in order to develope a rapid assay for Norovirus and to investigate the pathogenesis of virus.
目的制备诺如病毒衣壳蛋白特异性单克隆抗体，为诺如病毒的快速检测及致病机制的研究提供实验材料。
To prepare the monoclonal antibodies against Norovirus capsid protein in order to develope a rapid assay for Norovirus and to investigate the pathogenesis of virus.
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