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[Research of GFP-expressing H22 cells and S180 cells by electroblot in vitro and in vivo].

Fang Ma, Yuan Wang, Jie Zhao

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Abstract

Mouse hepatoma H22 cells and sarcoma cells (H22 and S180) were infected with EGFP-N1 by electroblot, and the acquired gfp-H22 and gfp-S180 cells expressing strong green fluorescence protein (GFP) fluorescence were supplemented with medium G418 Sigma (800 mg/ml). Meanwhile, the models bearing cancer (gfp H22 and gfp S180) subcutaneously and with abdominal cavity were established. There were no statistically significant differences by comparison on the cell phenotype, ultramicrostructure, growth curve and bearing cancer time between the H22 cells and S180 cells (P>0.05). The GFP fluorescence was detected with whole body GFP imaging system in vivo and with fluorescence microscope. According to the results of in vitro and in vivo assay, it was shown that, by application of fluorescence technology, the GFP-expressing H22 cells and S180 cells could be used in further studies on the tumor biological behavior.

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What this paper is about

Mouse hepatoma H22 cells and sarcoma cells (H22 and S180) were infected with EGFP-N1 by electroblot, and the acquired gfp-H22 and gfp-S180 cells expressing strong green fluorescence protein (GFP) fluorescence were supplemented with medium G418 Sigma (800 mg/ml). Meanwhile, the models bearing cancer (gfp H22 and gfp S180) subcutaneously and with abdominal cavity were established. There were no statistically significant differences by comparison on the cell phenotype, ultramicrostructure, growth curve and bearing cancer time between the H22 cells and S180 cells (P>0.05). The GFP fluorescence was detected with whole body GFP imaging system in vivo and with fluorescence microscope. According to the results of in vitro and in vivo assay, it was shown that, by application of fluorescence technology, the GFP-expressing H22 cells and S180 cells could be used in further studies on the tumor biological behavior.

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Available abstract

Mouse hepatoma H22 cells and sarcoma cells (H22 and S180) were infected with EGFP-N1 by electroblot, and the acquired gfp-H22 and gfp-S180 cells expressing strong green fluorescence protein (GFP) fluorescence were supplemented with medium G418 Sigma (800 mg/ml). Meanwhile, the models bearing cancer (gfp H22 and gfp S180) subcutaneously and with abdominal cavity were established. There were no statistically significant differences by comparison on the cell phenotype, ultramicrostructure, growth curve and bearing cancer time between the H22 cells and S180 cells (P>0.05). The GFP fluorescence was detected with whole body GFP imaging system in vivo and with fluorescence microscope. According to the results of in vitro and in vivo assay, it was shown that, by application of fluorescence technology, the GFP-expressing H22 cells and S180 cells could be used in further studies on the tumor biological behavior.

Key concepts: Green fluorescent protein, In vivo, In vitro, Fluorescence microscope, Fluorescence, Molecular biology, Cell culture, Chemistry

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[Research of GFP-expressing H22 cells and S180 cells by electroblot in vitro and in vivo]. — Research Paper | ScholarLens