Journals / Turkish Journal of Medical Sciences / 2011 / Cilt: 41 - Sayı: 5

An efficient method for stable transfection of mouse myogenic C2C12 cell line using a nonviral transfection approach

Pages
821–825
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: The T-RExTM system is useful in the development of stable cell lines for protein production or regulation of gene expression.

📌 3 Key Takeaways

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Objective & Hypothesis:To describe in detail the use of the T-RExTM System (a tetracycline-regulated mammalian expression system; Invitrogen) for rapid, easy, and effective generation of stable C2C12 cell clones.
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Key Findings & Data:Materials and methods: Generation of a stable C2C12 cell line was performed by stable transfection of the cells with the pcDNA6/TR plasmid vector, which contains the tetracycline repressor and the blasticidin drug resistance genes.
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Conclusion & Impact:Conclusion: The T-RExTM system is useful in the development of stable cell lines for protein production or regulation of gene expression.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: C2C12 cell line · stable transfection · inducible expression

Abstract

To describe in detail the use of the T-RExTM System (a tetracycline-regulated mammalian expression system; Invitrogen) for rapid, easy, and effective generation of stable C2C12 cell clones. Tetracycline-inducible stable cell lines are useful tools to study the function of various genes in different types of mammalian cells. However, the generation of stable cell lines is a time-consuming, technically difficult, and expensive process. Materials and methods: Generation of a stable C2C12 cell line was performed by stable transfection of the cells with the pcDNA6/TR plasmid vector, which contains the tetracycline repressor and the blasticidin drug resistance genes. The establishment of the stable cell line and the efficiency of the tetracycline-inducible gene expression system were shown with the transient transfection of reporter plasmid pTO-EGFP and observation of the GFP expression by fluorescence microscopy. Results: We established a stable T-RExTM C2C12 cell line that can be used for muscle research studies by transfecting the gene of interest with a second plasmid. Conclusion: The T-RExTM system is useful in the development of stable cell lines for protein production or regulation of gene expression.

Özet

To describe in detail the use of the T-RExTM System (a tetracycline-regulated mammalian expression system; Invitrogen) for rapid, easy, and effective generation of stable C2C12 cell clones. Tetracycline-inducible stable cell lines are useful tools to study the function of various genes in different types of mammalian cells. However, the generation of stable cell lines is a time-consuming, technically difficult, and expensive process. Materials and methods: Generation of a stable C2C12 cell line was performed by stable transfection of the cells with the pcDNA6/TR plasmid vector, which contains the tetracycline repressor and the blasticidin drug resistance genes. The establishment of the stable cell line and the efficiency of the tetracycline-inducible gene expression system were shown with the transient transfection of reporter plasmid pTO-EGFP and observation of the GFP expression by fluorescence microscopy. Results: We established a stable T-RExTM C2C12 cell line that can be used for muscle research studies by transfecting the gene of interest with a second plasmid. Conclusion: The T-RExTM system is useful in the development of stable cell lines for protein production or regulation of gene expression.

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Cite This Article

AKYÜZ, M. D., BALCI, B. H., DİNÇER, P. R. (2022). An efficient method for stable transfection of mouse myogenic C2C12 cell line using a nonviral transfection approach. Turkish Journal of Medical Sciences, Cilt: 41 - Sayı: 5, 821–825. https://ajindex.com/articles/611299

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