Electroporation-Mediated In Vitro Gene Delivery: An Electric Pulse Technique to Introduce Fluorescent Reporter Protein-Encoding Plasmids Into Cultured Cells

Published: April 30, 2023

Abstract

Source: Lo, J. C. W. et al., Efficient and Cost Effective Electroporation Method to Study Primary Cilium-Dependent Signaling Pathways in the Granule Cell Precursor. J. Vis. Exp.  (2021)

This video demonstrates the electroporation technique that introduces fluorescent protein-encoding plasmid DNA into mouse primary cerebellar granule cell precursors.

Protocol

1. Electroporation for Hh receptor transgene overexpression:  pEGFP-Smo For electroporation using a 2 mm gap cuvette, prepare the following plasmid-cell electroporation mixture for each reaction of electroporation: 1.2 × 106 mouse primary cerebellar granule cell precursors cells and 10 µg of pEGFP-mSmo (adjust the DNA stock concentration to ~2-5 µg/µL in Tris-EDTA buffer or sterile dH2O) in 100 µL of Opti-MEM.  <stro…

Disclosures

The authors have nothing to disclose.

Materials

B27 supplement Life Technologies LTD 17504044
GlutamMAXTM-I ,100x Gibco, Life Technologies 35050061 L-glutamine substitute
Matrigel BD Biosciences 354277 Basement membrane matrix
Neurobasal Gibco, Life Technologies 21103049
Poly-D-lysine Hydrobromide Sigma Aldrich P6407
CU 500 cuvette chamber Nepagene CU500
EPA Electroporation cuvette (2 mm gap) Nepagene EC-002
Opti-MEM Life Technologies LTD 31985070 Reduced-serum medium for transfection
pEGFP-mSmo Addgene 25395
Super Electroporator NEPA21 TYPE II In Vitro and In Vivo Electroporation Nepagene NEPA21 Electroporator

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Cite This Article
Electroporation-Mediated In Vitro Gene Delivery: An Electric Pulse Technique to Introduce Fluorescent Reporter Protein-Encoding Plasmids Into Cultured Cells. J. Vis. Exp. (Pending Publication), e20992, doi: (2023).

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