E7基因表达的检测采用RTPCR和间接免疫荧光实验。
The expression of E7 gene was examined by RT PCR and the indirect immunofluorescence.
间接免疫荧光检测和IMMS与细胞的结合实验证明，所构建的IMMS可有效地和靶细胞结合。
The results of indirect immunofluorescence and cell binding suggest that IMMS can effectively bind target cells while do not have nonspecific binding activity.
最后，对制备出的假病毒颗粒进行真核细胞感染实验，以间接免疫荧光法验证上述抗原的真核表达情况。
Immuno-fluorescence assay was used to confirm the expression of the recombinant proteins after virus infection in BHK21 cells.
最后，对制备出的假病毒颗粒进行真核细胞感染实验，以间接免疫荧光法验证上述抗原的真核表达情况。
Immuno-fluorescence assay was used to confirm the expression of the recombinant proteins after virus infection in BHK21 cells.
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