Cellular Reprogramming

Proprietary Footprint-Free RNA Reprogramming Method to Generate iPSCs.

Cellular Reprogramming with Pluristyx's Footprint-Free mRNA

Pluristyx has pioneered a proprietary approach to cellular reprogramming that utilizes a non-integrating, footprint-free method to generate induced Pluripotent Stem Cells (iPSCs). This innovative technique leverages the power of messenger RNA (mRNA) engineered to introduce and express transcription factors that transform adult cells into iPSCs resulting in direct cellular reprogramming. 

Donors appropriate
for clinical use

Pluristyx has worked hard to source regulatory-compliant donors that are appropriate for clinical use to generate high quality induced Pluripotent Stem Cells.  

Non-integrating, footprint-free mRNA technology

Pluristyx uses non-modified mRNA constructs that efficiently reprogram adult cells into genetically stable iPSCs.

Rigorously tested
to ensure success

Pluristyx's cellular reprogramming technique leverages mRNA that is engineered to express transcription factors to ensure successful reprogramming to iPSCs.

Freedom
to operate

Our proprietary mRNA cellular reprogramming technology provides groups with full Freedom to Operate for their chosen clinical indication and most major geographic territories.   

Donors appropriate
for clinical use

Pluristyx has worked hard to source regulatory-compliant donors that are appropriate for clinical use.  

Non-integrating, footprint-free mRNA technology

Pluristyx uses non-modified mRNA constructs that efficiently reprogram adult cells into genetically stable iPSCs.

Rigorously tested
to ensure success

Pluristyx uses non-modified mRNA constructs that efficiently reprogram adult cells into genetically stable iPSCs.   

Freedom
to Operate

Our proprietary mRNA reprogramming technology provides groups with full Freedom to Operate for their chosen clinical indication and most major geographic territories.   

mRNA Sequences

The heart of our technology lies in mRNA sequences that utilize non-modified nucleotides that organize into stable structures to provide long-lasting expression of transcription factors that guide somatic cells on their remarkable journey towards pluripotency.

Unlike traditional methods that rely on the integration of genetic material, Pluristyx's cellular reprogramming approach ensures a footprint-free process to produce early passage, genetically stable iPSCs that can be used as an ideal starting material for downstream genetic engineering and GMP manufacturing.  

Rigorously Tested to Ensure the Highest Quality

Pluristyx iPSCs are rigorously tested to ensure cell identity and consistently demonstrate their capacity to transform into various cell lineages, including neurons, cardiomyocytes, hepatocytes, and more. Our unmodified iPSCs then then selected based on their trilineage differentiation potential for the insertion of our FailSafe® and iACT Stealth Cells™ technologies, which provide the unparalleled safety and immune evasion abilities, respectively, that allows these cells to be used as the starting material for a multitude of therapeutic applications.   

Our commitment to innovation and excellence in cellular reprogramming ensures that Pluristyx's iPSCs stand at the forefront of regenerative medicine. Whether for drug discovery, disease modeling, or cell-based therapies, our proprietary footprint-free RNA cellular reprogramming method empowers researchers and clinicians with a powerful tool to unlock the full potential of induced pluripotent stem cells. Join us in revolutionizing the future of medicine, one reprogrammed cell at a time. 

Pluristyx's Cellular Reprogramming method transforms adult cells into iPSCS ensuring genetic stability

Rigorously Tested

Pluristyx iPSCs are rigorously tested and consistently demonstrate their capacity to transform into various cell lineages, including neurons, cardiomyocytes, hepatocytes, and more. Our unmodified iPSCs then then selected based on their trilineage differentiation potential for the insertion of our FailSafe® and iACT Stealth Cells™ technologies, which provide unparalleled safety and immune evasion abilities, respectively, that allows these cells to be used as the starting material for a multitude of therapeutic applications.   

Our commitment to innovation and excellence in cellular reprogramming ensures that Pluristyx's iPSCs stand at the forefront of regenerative medicine. Whether for drug discovery, disease modeling, or cell-based therapies, our proprietary footprint-free RNA reprogramming method empowers researchers and clinicians with a powerful tool to unlock the full potential of induced pluripotent stem cells. Join us in revolutionizing the future of medicine, one reprogrammed cell at a time. 

Pluristyx's Cellular Reprogramming method transforms adult cells into iPSCS ensuring genetic stability
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iACT Stealth Cells™

A groundbreaking technology that enables allograft transplantation without the need for systemic immune suppression
Our groundbreaking iACT technology with immune-modulatory genes allows the acceptance of allografts without the need for systemic immune suppression. Equipping pluripotent stem cells with this technology will allow the same cell line to be used for differentiation and ultimately transplantation into any individual.
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REA Process & Licensing

Try Before You Buy
By offering the Research Evaluation Agreement you can gain access to our modified and non-modified cellular products for evaluation with our Try Before You Buy model. A smaller upfront payment limits your risk. Once you see the successful results, you can then enter into a license agreement with us panCELLa / Pluristyx.
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Human Pluripotent Stem Cells

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Human pluripotent stem cells (hPSC) for use in R&D activities. Inquire for GMP grade cells suitable as a starting material in clinical applications. All cell lines are registered with the U.S. National Institutes of Health (NIH), are listed in the NIH Human Stem Cell Registry and are eligible for use in NIH-funded research.
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iACT Stealth Cells™

A groundbreaking technology that enables allograft transplantation without the need for systemic immune suppression
Our groundbreaking iACT technology with immune-modulatory genes allows the acceptance of allografts without the need for systemic immune suppression. Equipping pluripotent stem cells with this technology will allow the same cell line to be used for differentiation and ultimately transplantation into any individual.
Learn More

REA Process & Licensing

Try Before You Buy
By offering the Research Evaluation Agreement you can gain access to our modified and non-modified cellular products for evaluation with our Try Before You Buy model. A smaller upfront payment limits your risk. Once you see the successful results, you can then enter into a license agreement with us panCELLa / Pluristyx.
Learn More

Human Pluripotent Stem Cells

Product
Human pluripotent stem cells (hPSC) for use in R&D activities. Inquire for GMP grade cells suitable as a starting material in clinical applications. All cell lines are registered with the U.S. National Institutes of Health (NIH), are listed in the NIH Human Stem Cell Registry and are eligible for use in NIH-funded research.
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