The target gene couldn't express in NIH3T3 cells and blank control.
而转染鼠成纤维细胞NIH3T3，未见目的基因表达。
The mechanical scrape wound model of mouse NIH3T3 cells was used to identify the action on promoting the wound healing of this supernatant.
采用细胞机械创伤模型，检测此上清促进创伤愈合作用。
The objective of this study is to confirm the oncogenic and tumorigenic potential of the transformed NIH3T3 cells transfection mediated with TIF3.
本研究的目的是对TIF3基因转化NIH3T3细胞的致癌能力和致瘤性进行鉴定。
Addition of microencapsulated NGF expressing NIH3T3 cells could play good bridge and promotive role in regeneration of peripheral nerve and repair of nerve defect.
辅加转NGF基因3T3细胞对修复缺损的神经具有良好的桥梁作用和促神经生长作用。
We have obtained foci of transformed NIH3T3 cells through transfection of human DNA from CNE-2 (an undifferentiated epithelial cell line of nasopharyngeal carcinoma).
用低分化鼻咽癌细胞株CNE-2DNA转染NIH3T3细胞，获得的转化细胞株经扩增进行二轮和三轮转染。
CONCLUSION: a recombinant eukaryotic expression plasmid of amastin gene of Leishmania Donovani was successfully constructed, and can be expressed stably in the NIH3T3 cells.
结论：成功地构建杜氏利什曼原虫无鞭毛体蛋白基因的真核表达重组质粒，并且该基因在NIH3T3细胞中获得了稳定表达。
In this SFM SSV-NIH3T3 cells grow well, they keep the ability of secreting platelet-derived growth factor-like material into culture medium and causing tumor growth in nude mice.
在这个无血清培养基中，SSV -NIH3T3细胞可以很好地生长，并具有分泌血小板生长因子样生物学活性物质和致裸鼠肿瘤的能力。
The preliminary study showed that Malignant transformation of NIH3T3 cells have been induced by MNNG and the cell could be used to evaluate potential carcinogenicity of chemicals.
因此，初步认为NIH3T3细胞有可能作为评定化学物质转化作用的细胞株。
Meanwhile, normal NIH3T3 cells were taken as controls, and cultured by G418 contain MFD and by DMEM medium without G418 respectively. Light microscope was used to observe G418R NIH3T3 cells.
同时选用正常的NIH3T3细胞为对照，使用含有最小致死量g418及未加g 418的DMEM培养基进行培养，采用光学显微镜对G418抗性NIH3T3细胞进行观察。
AIM: to establish a NIH3T3 cell line which expresses human NT3 and to observe the growth of cochlear ganglion cells by co culturing.
目的：建立稳定表达nt3的NIH3T3细胞株，通过体外共培养实验观察其对耳蜗螺旋神经节细胞生长的影响。
AIM: to establish a NIH3T3 cell line which expresses human NT3 and to observe the growth of cochlear ganglion cells by co culturing.
目的：建立稳定表达nt3的NIH3T3细胞株，通过体外共培养实验观察其对耳蜗螺旋神经节细胞生长的影响。
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