Stem Cells

HighQC™ Human iPSC Line (Episomal, Fibroblast)

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  • High Purity Levels
  • Precision and Reliability
  • Customization Options
Species

Human

Cat.No

ABC-SC214Y

Quality Control

All cells test negative for mycoplasma, bacteria, yeast, and fungi.

Product Category Stem Cells
Size/Quantity

1 vial

Cell Type

Induced Pluripotent Stem Cell

Shipping Info

Dry Ice

Growth Conditions

37℃, 5% CO2

Source Organ

Human Skin Fibroblast

Disease

Normal

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human iPSCs

Description

HighQC™ Human iPSC Line (Episomal, Fibroblast) is a human induced pluripotent stem cell (iPSC) line generated using episomal-based reprogramming technology. This method involves the use of episomal vectors to introduce key reprogramming factors (such as OCT4, SOX2, KLF4, and c-MYC) into fibroblasts, inducing them to revert to a pluripotent state without integrating the vectors into the host genome. The resulting iPSCs exhibit typical pluripotent characteristics, including the expression of pluripotency markers like OCT4, SOX2, NANOG, and SSEA-4, and they are capable of forming embryoid bodies in culture. The Episomal vector remains in a non-integrated state within the cell and is naturally lost after reprogramming is complete, the adverse effects of long-term expression of reprogramming factors are reduced. HighQC™ Human iPSC Line (Episomal, Fibroblast) is suitable for a variety of applications, including disease modeling, drug discovery, and cell-based therapies.

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Citation

When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).

Application

  • HighQC™ Human iPSC Line (Episomal, Fibroblast) is ideal for disease modeling, drug discovery, and regenerative medicine. Due to its non-integrating nature, it is widely used in gene therapy research and cell-based therapy development. Specific applications include studying genetic diseases such as cystic fibrosis and ALS, developing new antiviral drugs, or conducting regenerative research for liver and retinal diseases.

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
Customization Options
Tailed to your research

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