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- W2391168343 abstract "Objective: To explore the feasiability of using EGFP labeling stem cell.Methods: A recombinant vector EGFP-pLNCX2 was obtained by using standard molecular cloning techniques.The virus was directly transfected cavy MSCs.MSCs were induced into neuron-like cells.NF was tested and compared with non-transfected MSCs.Results: The recombinant vector was successfully contructed.EGFP expressed steadily in cavy MSC for more than a month.Transfected MSCs keep the ability to express NF when induced.Conclusions: The recombinant vector can be readily constructed and the tranfection of EGFP does not influence differentiation potential of MSC,which suggests that EGFP may be an ideal tool for labeling stem cells." @default.
- W2391168343 created "2016-06-24" @default.
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- W2391168343 date "2005-01-01" @default.
- W2391168343 modified "2023-09-23" @default.
- W2391168343 title "Study of cuinea pig mesenchymal stem cell tranfected with EGFP gene in vitro" @default.
- W2391168343 hasPublicationYear "2005" @default.
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