Episomal iPSC Reprogramming System

Make transgene-free iPSCs suitable for in vivo applications with this kit that provides a non-viral, non-integrating plasmid system

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Episomal iPSC Reprogramming System

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Episomal iPSC Reprogramming System

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5 Reactions
SC900A-1
$ 808
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1-888-266-5066

Overview

Placing the power of iPSCs into your hands

When you’re using stem cells for modeling disease, discovering and developing new drugs, or building novel cell-based therapeutics, reliable generation of iPSCs is critical. Even better if the iPSCs are transgene-free. With SBI’s Episomal iPSC Reprogramming System you can quickly and efficiently reprogram human or mouse cells for a range of in vivo applications.

  • Ideal for in vivo studies—iPSC generation that’s virus-free and footprint-free
  • Efficient—get 70% more iPSC colonies than when using standard retroviral methods
  • Fast—iPSC colony formation is complete in 25 days
  • Flexible—works with both feeder and feeder-free conditions
  • Easy—a simple, hands-free workflow for reliable reprogramming

SBI’s Episomal iPSC Reprogramming System is based on the Epstein-Barr Nuclear Antigen-1 plasmid system (oriP/EBNA-1) that has been proven to reliably and efficiently generate iPSCs free from the risk of integrated transgenic sequences1. The system works efficiently with patient fibroblasts and blood cells2, and can even generate iPSCs from difficult-to-reprogram source cells like older patient fibroblasts (Figure 1).

pCDH-CuO-MCS-IRES-GFP-EF1α-CymR-T2A-Puro SparQ All-in-one Cloning and Expression Lentivector

Figure 1. Reprogram difficult source cells with the Episomal iPSC Reprogramming System. Successful iPSC reprogramming of eight-times passaged human dermal fibroblasts from a sixty-year-old patient sample is achieved with SBI’s Episomal iPSC Reprgramming System (left panel), but not with the standard Yamanaka OSKM factors (right panel).

The system contains Oct4, Sox2, Klf4, L-myc, Lin28, shRNA-p53, and miR302/367 cluster reprogramming factors, along with a GFP marker for monitoring transfection efficiency and plasmid loss over time. Unlike traditional plasmid systems, the oriP/EBNA-1 system replicates in synchrony with the host genome by anchoring itself to chromatin and replicating during each cell cycle divisions. The episomal plasmids are naturally lost at up to 5% per cell division cycle, with most cells losing the episome completely by passage fifteen.

References

  1. Okita K, et al. A more efficient method to generate integration-free human iPS cells. Nat Methods. 2011 May; 8(5):409-12. PMID: 21460823.
  2. Schlaeger, et al. A comparison of non-integrating reprogramming methods. Nat Biotechnol. 2015 Jan; 33(1):58-63. PMCID: PMC4329913.

How It Works

A simple workflow for integration-free, virus-free reprogramming

Simply transfect your cells with the Episomal iPSC Reprogramming System Plasmids and culture. Transfection efficiency can be monitored with the co-expressed GFP marker.

A simple workflow for integration-free, virus-free reprogramming

Supporting Data

Rapid and robust reprogramming with the Episomal iPSC Reprogramming System

Visible iPSC colony formation can be observed in as little as two weeks after transfection and is complete in 25 days, with 70% more iPSC colonies generated compared to standard OSKM methods

Figure 2. The Episomal iPSC Reprogramming system delivers visible colonies in as little as two weeks and is complete in twenty-five days. Human adult primary dermal fibroblasts electroporated with the Episomal iPSC System and cultured for (A) 24 hours, or (B) the time indicated on each panel. After 25 days, 70% more iPSC colonies are generated compared to standard OSKM methods.

Staining with alkaline phosphatase and immunostaining show that robust and healthy iPSCs are generated by the Episomal iPSC Reprogramming System.

Figure 3. Robust and healthy iPSCs are generated by the Episomal iPSC Reprogramming System. Colonies generated by the Episomal iPSC System clearly display the morphology of reprogrammed cells and express stem cell-specific markers as shown by staining with alkaline phosphatase and immunostaining for the pluripotency markers Nanog, Oct4, Sox2, SSEA3, TRA-1-60 and TRA-1-81, as indicated.