Ingenio EZporator Electroporation System
Ingenio EZporator Electroporation System
Brand: Mirus Bio
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Ingenio EZporator Electroporation System
Easy to use and cost effective electroporation system for high efficiency transfection of mammalian cells
This system is designed to be used with the Ingenio® Electroporation Solution which is ideal for mammalian and insect cell transfection. Electroporation is the method of choice for many hard-to-transfect cell types, and the Ingenio® EZporator® Electroporation System is a cost-effective, straightforward, open system that is perfect for any lab seeking performance without breaking the bank.
- Performance: deliver any nucleic acid to hard-to-transfect, stem and primary cells
- Simplicity: use a single, universal electroporation solution across all cell types
- Flexibility: easily optimize electroporation parameters for each cell type
- Every system comes with a complimentary Ingenio® Electroporation Kit (8 reactions) and an easy-to-use protocol
Figures and Data
High Efficiency Electroporation with the Ingenio® EZporator® Electroporation System. Jurkat E6-1 (A), K562 (B), Raji (C), or Raw 264.7 (D) cells were electroporated with an EGFP reporter plasmid at various voltages using the Ingenio® Electroporation Solution (Mirus Bio) and the Ingenio® EZporator® Electroporation System (Mirus Bio) using either 0.2 cm or 0.4 cm electroporation cuvettes. The percentage of GFP positive cells (bar) and viability (dot) using propidium iodide was determined by flow cytometry at 48 hours post-electroporation.
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Figures and Data
High Efficiency Electroporation with the Ingenio® EZporator® Electroporation System. Jurkat E6-1 (A), K562 (B), Raji (C), or Raw 264.7 (D) cells were electroporated with an EGFP reporter plasmid at various voltages using the Ingenio® Electroporation Solution (Mirus Bio) and the Ingenio® EZporator® Electroporation System (Mirus Bio) using either 0.2 cm or 0.4 cm electroporation cuvettes. The percentage of GFP positive cells (bar) and viability (dot) using propidium iodide was determined by flow cytometry at 48 hours post-electroporation.
