Ingenio® Electroporation Products

High efficiency electroporation using any instrument

 

Looking for an electroporation device?
Mirus now offers the Ingenio® EZporator® Electroporation Systemdesigned for simple, high efficiency electroporation.

 

To inquire about bulk pricing, please call 888-530-0801
International inquiries please call +1-608-441-2852
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Choose a Product:

Ingenio® Electroporation SolutionIngenio® Electroporation Kit for the EZporator® Electroporation System and Lonza-Amaxa® Nucleofector® II/2b devices (0.2 cm cuvettes and cell droppers)Ingenio® Electroporation Kits for the EZporator® Electroporation System and all conventional electroporators such as Bio-Rad® and Harvard-BTX® (0.4 cm cuvettes and cell droppers)

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MIR 5011125 reactionsMIR 5011450 reactionsMIR 50117100 reactions

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Note: Ingenio® Solution is compatible with all electroporators including Amaxa®'s Nucleofector® Device.

  • High Efficiency Electroporation– Deliver to hard to transfect cell lines and primary cells
  • Compatible with Most Conventional Electroporation Devices – Use your existing system including the Ingenio® EZporator®, Lonza-Amaxa®, Bio-Rad® or Harvard BTX®
  • Save Money and Reduce Research Costs Without Sacrificing Performance – Ingenio® Electroporation Solution is available as a stand-alone solution or as part of a complete kit with cuvettes and cell droppers

Looking for a high quality, cost-effective electroporation device?

Mirus now offers the new Ingenio® EZporator® Electroporation System, perfect for labs seeking high performance without breaking the bank. 

NEW PROTOCOL
Electroporation of Human Induced Pluripotent Stem (iPS) Cells with Ingenio® Electroporation Solution

Ingenio® Pulse Condition Recommendations
Electroporating Primary cells and Other Hard to Transfect Cell Types using Ingenio® Electroporation Solution
Electroporation of Human Induced Pluripotent Stem (iPS) Cells with Ingenio® Electroporation Solution

 

Figures and Data

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CRISPR RNP Delivery with Ingenio Electroporation Solution Targeting PPIB

CRISPR RNP Delivery with Ingenio® Electroporation Solution. K562 and Jurkat cells were electroporated with a Cas9 protein/gRNA, ribonucleoprotein (RNP) complex, composed of 750 nM Cas9 protein (EnGen® Cas9 NLS, NEB) and 1500 nM pre-complexed two-part gRNA (IDT) targeting PPIB using the Ingenio® Electroporation Solution and a Gene Pulser Xcell™ Eukaryotic System. Exponential pulse conditions of 130V, 950 µF for K562 and 150V, 950 µF for Jurkat cells were applied to triplicate 0.2 cm cuvettes, 100 µl volume, 10 x 106 cells/ml +/- RNP complex. A T7E1 mismatch assay was used to measure cleavage efficiency at 48 hours post-transfection. Non-specific bands (NSP) were observed in the negative control of both cell lines. Cleavage efficiency was calculated based on the ratio of cleaved band intensities to the sum of cleaved and uncleaved band intensities minus the average signal of the non-specific band(s) in negative control lanes.

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High Efficiency Plasmid DNA Electroporation of Human Induced Pluripotent Stem (iPS) Cells Using Ingenio

High Efficiency Plasmid DNA Electroporation of Human Induced Pluripotent Stem (iPS) Cells Using Ingenio®. The Ingenio® Electroporation Kit was used to transfect 2 x 106 iPS cells on the Amaxa® Nucleofector® II Device. Cells were electroporated with 8 µg ZsGreen expressing plasmid (Clontech) in 100 µl and plated in 6-well plates at 0.33 x 106 cells/well. Cells were visualized 24 hours post-transfection and imaged under 4X objective with an Olympus IX71® Inverted Microscope. Images are (A) phase contrast, and (B) green fluorescence. Cells were also assayed 24 hours post-transfection on an Accuri® Cytometer. The histogram (C) shows unelectroporated cells (black line) compared to cells electroporated with plasmid using the Ingenio® Electroporation Kit (green line). See more information on stem cell applications.

Data courtesy of
CDI logo

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Ingenio Solution Provides Comparable Efficiency on Amaxa Nucleofector Device

Ingenio® Solution Provides Comparable Efficiency on Amaxa® Nucleofector® Device. Cells were electroporated in parallel with an EGFP reporter vector using a Nucleofector® II Device (Amaxa®) and either the Ingenio® Electroporation Solution or the Nucleofector® Kit V (Amaxa®) according to Amaxa®’s recommended protocol for each cell line [HL-60 (T-019), Jurkat E6-1(X-001), K-562 (T-016), THP-1 (V-001), SK-N-MC (A-023), and MCF-7 (P020)]. EGFP expressing cells were identified 24 hours post-electroporation by flow cytometry and presented as a percentage of the live cell population.

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Efficient Plasmid DNA Delivery Using Ingenio Solution with Amaxa Nucleofector Device

Efficient Plasmid DNA Delivery Using Ingenio® Solution with Amaxa® Nucleofector® Device. Ingenio® Electroporation Kits were used to transfect indicated cell types using Amaxa® Nucleofector® II Device. Cells were assayed at 24 hours by flow cytometry and reported as percentage of live cell population. See the recommended experimental conditions.

*Primary cell types

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Ingenio Outperforms Other Electroporation Solutions in Efficiency and Viability

Ingenio® Outperforms Other Electroporation Solutions in Efficiency and Viability. Cells were electroporated in parallel with an EGFP reporter vector using either Ingenio® Electroporation Solution, PBS or the Gene Pulser Electroporation Buffer (Bio-Rad®) on the Gene Pulser Xcell™ Eukaryotic System. (A) EGFP expressing cells were identified 24 hours post-electroporation by flow cytometry and presented as a percentage of the live cell population. (B) Cells were assayed for viability by propidium iodide staining and flow cytometry analysis. Experiments were performed in triplicate on three separate days and the data averaged.

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Ingenio Provides High Efficiency Electroporation of Hard to Transfect Cell Lines

Using Standard Electroporators, Ingenio® Provides High Efficiency Electroporation of Hard to Transfect Cell Lines. Cells were electroporated with an EGFP reporter vector using the Ingenio® Electroporation Solution and a Gene Pulser Xcell™ Eukaryotic System. EGFP expressing cells were identified 24 hours post-electroporation by flow cytometry and presented as a percentage of the live cell population. See the recommended pulse conditions.

Resources

Specifications

Storage Conditions:
All Configurations: Store solution at 4°C, store cuvettes and droppers at room temperature

Product Guarantee:
All Configurations: 1 year

Usage Statement:
All Configurations: For Research Use Only.

Animal Origin Statement:
All Configurations: This product is animal origin free.

Technical Product Literature


Additional Resources

COA Lookup

Download Certificates of Analysis

COO Lookup

Download Certificate of Origin

Testimonials

I have been using the Ingenio® Electroporation Solution to generate knockouts using the CRISPR/Cas system in primary neural stem cells. The transfection efficiency is comparable to the Amaxa® kit, and knockout generation is quite efficient using wt-Cas9 plasmids. Multiple gRNAs have yielded comparable efficiency.
Simon Weissman
Biotech Research and Innovation Centre, Denmark
I like the Ingenio® Electroporation Solution a lot. It is simple, efficient and reasonably priced. Also, I like that you can use it with multiple different instruments. The Ingenio® EZporator® Electroporation system worked great for our lab too. I love that you have some control over the electroporation settings, but its not too complicated.
Artem Nemudryi
Montana State University
I was very depressed for the last 6 months because I was unable to transfect my rat cell line with various transfection reagents. I tried 5 Nucleofection® programs, 2 buffers and several different cell densities. But nothing worked. I am very happy to inform you, Ingenio® is a life saver!
Sanal Madhusudana Girija
Albert Einstein College of Medicine
The Ingenio® Electroporation Kit is routinely used in our lab to transfect induced pluripotent stem cells (iPSCs) via electroporation and yields extremely high transfection efficiency. The Ingenio® Kit is entirely compatible with the Amaxa® Nucleofector® and is also a much more cost effective solution.
Elizabeth Dominguez
Cellular Dynamics International (CDI)