Methods The human embryo cerebral neurons were prepared for the primary culture using light microscope, tissue staining after inocula-ting HCMV of TCID50.
方法采用人胚脑神经细胞原代培养，接种TCID50的HCMV后用光镜、组织染色观察病变全过程。
Methods The human embryo cerebral neurons were prepared for the primary culture using light microscope, tissue staining after inocula-ting HCMV of TCID50.
方法采用人胚脑神经细胞原代培养，接种TCID50的HCMV后用光镜、组织染色观察病变全过程。
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